DB code: S00021
RLCP classification | 1.30.300.2 : Hydrolysis | |
---|---|---|
CATH domain | 1.10.530.40 : Lysozyme | Catalytic domain |
E.C. | 3.2.1.17 | |
CSA | 206l | |
M-CSA | 206l | |
MACiE |
CATH domain | Related DB codes (homologues) |
---|---|
1.10.530.40 : Lysozyme | S00265 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | CAZy | Pfam |
---|---|---|---|---|---|
P00720 |
Lysozyme
|
EC
3.2.1.17
Lysis protein Muramidase Endolysin |
NP_049736.1
(Protein)
NC_000866.4 (DNA/RNA sequence) |
GH24
(Glycoside Hydrolase Family 24)
|
PF00959
(Phage_lysozyme)
[Graphical View] |
KEGG enzyme name |
---|
lysozyme
muramidase globulin G mucopeptide glucohydrolase globulin G1 N,O-diacetylmuramidase lysozyme g L-7001 1,4-N-acetylmuramidase mucopeptide N-acetylmuramoylhydrolase PR1-lysozyme |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P00720 | LYS_BPT4 | Hydrolysis of (1->4)-beta-linkages between N- acetylmuramic acid and N-acetyl-D-glucosamine residues in a peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrins. |
KEGG Pathways | Map code | Pathways | E.C. |
---|
Compound table | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Substrates | Products | Intermediates | ||||||||||
KEGG-id | C00851 | C00889 | C00001 | C00851 | C04394 | C00140 | ||||||
E.C. | ||||||||||||
Compound | Chitodextrin | Peptidoglycan | H2O | Chitodextrin | Peptidoglycan(N-acetyl-D-glucosamine) | N-Acetyl-D-glucosamine | ||||||
Type | amide group,polysaccharide | amino acids,amide group,amine group,carbohydrate,peptide/protein,polysaccharide | H2O | amide group,polysaccharide | amino acids,amide group,amine group,carbohydrate,lipid,peptide/protein,polysaccharide | amide group,carbohydrate | ||||||
ChEBI |
15377 15377 |
8006 8006 |
506227 506227 |
|||||||||
PubChem |
22247451 962 22247451 962 |
5462260 5462260 |
439174 439174 |
|||||||||
102lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
103lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
104lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
104lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
107lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
108lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
109lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
110lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
111lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
112lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
113lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
114lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
115lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
116lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
116lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
116lC | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
116lD | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
118lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
119lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
120lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
122lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
123lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
125lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
126lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
127lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
128lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
129lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
130lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
131lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
137lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
137lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
138lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
139lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
140lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
141lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
142lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
143lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
144lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
145lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
146lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
147lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
148lE | Unbound | Unbound | Unbound | Unbound | Unbound | Intermediate-analogue:NAG-AMU-ALA-GLU-API-ALA (chain S:covalent bond with mutated residue Glu26) | ||||||
149lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
150lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
150lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
150lC | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
150lD | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
151lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
152lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
155lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
156lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
157lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
158lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
159lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
160lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
161lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
162lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
163lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
164lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
165lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
166lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
167lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
167lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
168lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
168lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
168lC | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
168lD | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
168lE | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
169lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
169lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
169lC | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
169lD | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
169lE | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
170lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
171lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
172lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
173lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
174lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
174lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
175lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
175lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
176lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
176lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
177lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
178lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
179lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
180lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
180lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
181lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
182lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
183lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
184lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
185lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
186lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
187lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
188lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
189lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
190lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
191lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
192lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
195lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
196lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
197lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
198lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
199lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1b6iA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c60A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c61A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c62A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c63A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c64A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c65A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c66A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c67A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c68A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c69A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6aA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6bA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6cA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6dA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6eA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6fA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6gA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6hA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6iA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6jA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6kA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6mA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6nA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6pA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6qA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1c6tA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1ctwA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cu0A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cu2A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cu3A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cu5A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cu6A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cupA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cuqA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv0A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv1A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv3A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv4A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv5A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cv6A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cvkA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cx6A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1cx7A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d2wA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d2yA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d3fA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d3jA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d3mA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d3nA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1d9wA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dyaA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dybA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dycA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dydA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dyeA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dyfA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1dygA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1epyA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l00A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l01A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l02A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l03A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l04A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l05A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l06A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l07A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l08A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l09A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l10A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l11A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l12A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l13A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l14A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l15A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l16A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l17A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l18A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l19A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l20A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l21A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l22A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l23A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l24A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l25A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l26A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l27A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l28A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l29A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l30A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l31A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l32A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l33A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l34A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l35A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l36A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l37A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l38A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l39A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l40A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l41A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l42A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l43A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l44A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l45A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l46A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l47A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l48A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l49A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l50A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l51A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l52A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l53A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l54A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l55A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l56A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l57A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l58A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l59A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l60A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l61A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l62A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l63A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l64A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l65A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l66A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l67A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l68A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l69A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l70A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l71A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l72A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l73A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l74A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l75A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l76A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l77A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l79A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l80A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l81A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l82A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l83A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l84A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l85A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l86A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l87A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l88A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l89A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l90A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l91A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l92A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l93A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l94A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l95A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l96A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l97A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l97B | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l98A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1l99A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lydA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lyeA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lyfA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lygA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lyhA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lyiA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1lyjA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1nhbA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qs5A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qs9A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qsbA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qsqA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt3A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt4A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt5A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt6A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt7A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qt8A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qtbA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qtcA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qtdA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qthA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qthB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qtvA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qtzA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qudA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1qugA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1quhA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1quoA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1tlaA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
200lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
201lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
201lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
205lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
206lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
209lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
210lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
211lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
212lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
213lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
214lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
215lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
216lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
216lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
217lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
218lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
219lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
220lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
221lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
222lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
223lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
224lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
225lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
226lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
227lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
228lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
229lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
230lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
231lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
232lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
233lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
234lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
235lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
236lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
237lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
238lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
239lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
240lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
241lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
242lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
243lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
244lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
245lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
246lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
247lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
248lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
249lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
250lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
251lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
252lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
253lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
254lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
255lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
256lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
257lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
258lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
259lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
260lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
262lA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
262lB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
2l78A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
2lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
3lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
4lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
5lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
6lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
7lzmA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
Swiss-prot;LYCV_BPT4;P00720 |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
102lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion N40-A | ||||||||
103lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion N40-SLD | ||||||||
104lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion S44-AA | ||||||||
104lB | GLU 11;ASP 20 | mutant C54T, C97A, insertion S44-AA | ||||||||
107lA | GLU 11;ASP 20 | mutant S44G, C54T, C97A | ||||||||
108lA | GLU 11;ASP 20 | mutant S44I, C54T, C97A | ||||||||
109lA | GLU 11;ASP 20 | mutant S44K, C54T, C97A | ||||||||
110lA | GLU 11;ASP 20 | mutant S44L, C54T, C97A | ||||||||
111lA | GLU 11;ASP 20 | mutant S44N, C54T, C97A | ||||||||
112lA | GLU 11;ASP 20 | mutant S44P, C54T, C97A | ||||||||
113lA | GLU 11;ASP 20 | mutant S44R, C54T, C97A | ||||||||
114lA | GLU 11;ASP 20 | mutant S44T, C54T, C97A | ||||||||
115lA | GLU 11;ASP 20 | mutant S44V, C54T, C97A | ||||||||
116lA | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
116lB | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
116lC | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
116lD | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
118lA | GLU 11;ASP 20 | mutant C54T, C97A, A130S | ||||||||
119lA | GLU 11;ASP 20 | mutant C54T, C97A, A134S | ||||||||
120lA | GLU 11;ASP 20 | mutant A41S, C54T, C97A | ||||||||
122lA | GLU 11;ASP 20 | mutant C54T, A73S, C97A | ||||||||
123lA | GLU 11;ASP 20 | mutant C54T, A82S, C97A | ||||||||
125lA | GLU 11;ASP 20 | mutant C54T, C97A, A98S | ||||||||
126lA | GLU 11;ASP 20 | mutant C54T, C97A, V149T | ||||||||
127lA | GLU 11;ASP 20 | mutant C54T, V75T, C97A | ||||||||
128lA | GLU 11;ASP 20 | mutant C54T, V87T, C97A | ||||||||
129lA | GLU 11;ASP 20 | mutant C54T, A93T, C97A | ||||||||
130lA | GLU 11;ASP 20 | mutant C54T, C97A, T151S | ||||||||
131lA | GLU 11;ASP 20 | mutant T26S, C54T, C97A | ||||||||
137lA | GLU 11;ASP 20 | mutant S44F, C54T, C97A | ||||||||
137lB | GLU 11;ASP 20 | mutant S44F, C54T, C97A | ||||||||
138lA | GLU 11;ASP 20 | mutant C54T, A93C, C97A | ||||||||
139lA | GLU 11;ASP 20 | mutant C54T, N68C, A93C, C97A | ||||||||
140lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129M, F153L | ||||||||
141lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129M, V149I | ||||||||
142lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129V, L133A, F153L | ||||||||
143lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129V, L133M, F153L | ||||||||
144lA | GLU 11;ASP 20 | mutant C54T, C97A, L121I, A129L, L133M, F153W | ||||||||
145lA | GLU 11;ASP 20 | mutant C54T, C97A, L121I, A129W, L133M | ||||||||
146lA | GLU 11;ASP 20 | mutant C54T, C97A, L121M, A129L, L133M, V149I, F153W | ||||||||
147lA | GLU 11;ASP 20 | mutant C54T, C97A, L121M, L133V, F153L | ||||||||
148lE | GLU 11;ASP 20 | mutant T26E, C54T, C97A | ||||||||
149lA | GLU 11;ASP 20 | mutant I3L | ||||||||
150lA | GLU 11;ASP 20 | mutant M6I | ||||||||
150lB | GLU 11;ASP 20 | mutant M6I | ||||||||
150lC | GLU 11;ASP 20 | mutant M6I | ||||||||
150lD | GLU 11;ASP 20 | mutant M6I | ||||||||
151lA | GLU 11;ASP 20 | mutant T34A, K35A, S36A, P37A | ||||||||
152lA | GLU 11;ASP 20 | mutant I3C, I9C, T21C, C54T, T142C, L164C | ||||||||
155lA | GLU 11;ASP 20 | mutant C54T, C97A, T115A, S117A | ||||||||
156lA | GLU 11;ASP 20 | mutant C54T, A97A, T115A, R119A | ||||||||
157lA | GLU 11;ASP 20 | mutant C54T, C97A, T115A, N116A, S117A, R119A, M120A, Q122A, Q123A | ||||||||
158lA | GLU 11;ASP 20 | mutant C54T, C97A, S117A, R119A | ||||||||
159lA | GLU 11;ASP 20 | mutant C54T, C97A, R119A, Q123A | ||||||||
160lA | GLU 11;ASP 20 | mutant C54T, C97A, M120A | ||||||||
161lA | GLU 11;ASP 20 | mutant C54T, C97A, N116A | ||||||||
162lA | GLU 11;ASP 20 | mutant C54T, C97A, Q122A | ||||||||
163lA | GLU 11;ASP 20 | mutant C54T, C97A, Q123A | ||||||||
164lA | GLU 11;ASP 20 | mutant C54T, C97A, R119A | ||||||||
165lA | GLU 11;ASP 20 | mutant C54T, C97A, S117A | ||||||||
166lA | GLU 11;ASP 20 | mutant C54T, C97A, T115A | ||||||||
167lA | GLU 11;ASP 20 | mutant I3C, I9C, C54T, L164C | ||||||||
167lB | GLU 11;ASP 20 | mutant I3C, I9C, C54T, L164C | ||||||||
168lA | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A | ||||||||
168lB | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A | ||||||||
168lC | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A | ||||||||
168lD | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A | ||||||||
168lE | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A | ||||||||
169lA | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A, Y139A, N140A, Q141A | ||||||||
169lB | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A, Y139A, N140A, Q141A | ||||||||
169lC | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A, Y139A, N140A, Q141A | ||||||||
169lD | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A, Y139A, N140A, Q141A | ||||||||
169lE | GLU 11;ASP 20 | mutant E128A, V131A, N132A, K135A, S136A, R137A, Y139A, N140A, Q141A | ||||||||
170lA | GLU 11;ASP 20 | mutant C54S, C97S, A146C | ||||||||
171lA | GLU 11;ASP 20 | mutant E45A, C54T, C97A | ||||||||
172lA | GLU 11;ASP 20 | mutant I3C | ||||||||
173lA | GLU 11;ASP 20 | mutant K16E, R119E, K135E, K147E | ||||||||
174lA | GLU 11;ASP 20 | mutant T34A, K35A, S36A, P37A, S38D, N40A, S44A, E45A, D47A, K48A, C54T, T97A | ||||||||
174lB | GLU 11;ASP 20 | mutant T34A, K35A, S36A, P37A, S38D, N40A, S44A, E45A, D47A, K48A, C54T, T97A | ||||||||
175lA | GLU 11;ASP 20 | mutant C54T, R96A, C97A | ||||||||
175lB | GLU 11;ASP 20 | mutant C54T, R96A, C97A | ||||||||
176lA | GLU 11;ASP 20 | mutant L32T, T34K, K35V, S36D, P37G, S38N, L39S, C54T, C97A | ||||||||
176lB | GLU 11;ASP 20 | mutant L32T, T34K, K35V, S36D, P37G, S38N, L39S, C54T, C97A | ||||||||
177lA | GLU 11;ASP 20 | mutant C54T, C97A, D127C, R154C | ||||||||
178lA | GLU 11;ASP 20 | mutant C54T, C97A, D127C, R154C | ||||||||
179lA | GLU 11;ASP 20 | mutant C54A, C97A, D127C, R154C | ||||||||
180lA | GLU 11;ASP 20 | mutant T26E, C54T, C97A | ||||||||
180lB | GLU 11;ASP 20 | mutant T26E, C54T, C97A | ||||||||
181lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
182lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
183lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
184lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
185lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
186lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
187lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
188lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
189lA | GLU 11;ASP 20 | mutant I3L, S38D, A41V, A82P, N116D, V131A, N144D | ||||||||
190lA | GLU 11;ASP 20 | mutant N53A, N55A, V57A | ||||||||
191lA | GLU 11;ASP 20 | mutant N53A, N55A, V57A, E128A, V131A, N132A | ||||||||
192lA | GLU 11;ASP 20 | mutant N40A, S44A, E45A, D47A, K48A, C54T, C97A, D127A, E128A, V131A, N132A | ||||||||
195lA | GLU 11;ASP 20 | mutant C54T, C97A, A129L | ||||||||
196lA | GLU 11;ASP 20 | mutant C54T, C97A, A129M | ||||||||
197lA | GLU 11;ASP 20 | mutant C54T, C97A, A129M, F153A | ||||||||
198lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129L | ||||||||
199lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, A129M | ||||||||
1b6iA | GLU 11;ASP 20 | mutant C54T, C97A, T21C, K124C | ||||||||
1c60A | GLU 11;ASP 20 | mutant C54T, C97A, F153A | ||||||||
1c61A | GLU 11;ASP 20 | mutant C54T, C97A, F153A | ||||||||
1c62A | GLU 11;ASP 20 | mutant C54T, C97A, F153A | ||||||||
1c63A | GLU 11;ASP 20 | mutant C54T, C97A, L121A | ||||||||
1c64A | GLU 11;ASP 20 | mutant C54T, C97A, L121A | ||||||||
1c65A | GLU 11;ASP 20 | mutant C54T, C97A, L121A | ||||||||
1c66A | GLU 11;ASP 20 | mutant C54T, C97A, L121A, L133A | ||||||||
1c67A | GLU 11;ASP 20 | mutant C54T, C97A, L121A, L133A | ||||||||
1c68A | GLU 11;ASP 20 | mutant C54T, C97A, L121A, L133A | ||||||||
1c69A | GLU 11;ASP 20 | mutant C54T, C97A, L133A | ||||||||
1c6aA | GLU 11;ASP 20 | mutant C54T, C97A, L133A | ||||||||
1c6bA | GLU 11;ASP 20 | mutant C54T, C97A, L133A | ||||||||
1c6cA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6dA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6eA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6fA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6gA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6hA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6iA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6jA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6kA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1c6lA | GLU 11;ASP 20 | mutant C54T, C97A, L99A, F153A | ||||||||
1c6mA | GLU 11;ASP 20 | mutant C54T, C97A, L99A, F153A | ||||||||
1c6nA | GLU 11;ASP 20 | mutant C54T, C97A, L99A, F153A | ||||||||
1c6pA | GLU 11;ASP 20 | mutant C54T, C97A | ||||||||
1c6qA | GLU 11;ASP 20 | mutant C54T, C97A | ||||||||
1c6tA | GLU 11;ASP 20 | mutant C54T, C97A | ||||||||
1ctwA | GLU 11;ASP 20 | mutant I78A | ||||||||
1cu0A | GLU 11;ASP 20 | mutant I78M | ||||||||
1cu2A | GLU 11;ASP 20 | mutant I84M | ||||||||
1cu3A | GLU 11;ASP 20 | mutant V87M | ||||||||
1cu5A | GLU 11;ASP 20 | mutant L91M | ||||||||
1cu6A | GLU 11;ASP 20 | mutant L91A | ||||||||
1cupA | GLU 11;ASP 20 | |||||||||
1cuqA | GLU 11;ASP 20 | mutant V103M | ||||||||
1cv0A | GLU 11;ASP 20 | mutant F104M | ||||||||
1cv1A | GLU 11;ASP 20 | mutant V111M | ||||||||
1cv3A | GLU 11;ASP 20 | mutant L121M | ||||||||
1cv4A | GLU 11;ASP 20 | mutant L118M | ||||||||
1cv5A | GLU 11;ASP 20 | mutant L133M | ||||||||
1cv6A | GLU 11;ASP 20 | mutant V149M | ||||||||
1cvkA | GLU 11;ASP 20 | mutant L118A | ||||||||
1cx6A | GLU 11;ASP 20 | |||||||||
1cx7A | GLU 11;ASP 20 | |||||||||
1d2wA | GLU 11;ASP 20 | |||||||||
1d2yA | GLU 11;ASP 20 | |||||||||
1d3fA | GLU 11;ASP 20 | |||||||||
1d3jA | GLU 11;ASP 20 | |||||||||
1d3mA | GLU 11;ASP 20 | |||||||||
1d3nA | GLU 11;ASP 20 | |||||||||
1d9wA | GLU 11;ASP 20 | |||||||||
1dyaA | GLU 11;ASP 20 | mutant V131D | ||||||||
1dybA | GLU 11;ASP 20 | mutant V131G | ||||||||
1dycA | GLU 11;ASP 20 | mutant V131I | ||||||||
1dydA | GLU 11;ASP 20 | mutant V131L | ||||||||
1dyeA | GLU 11;ASP 20 | mutant V131S | ||||||||
1dyfA | GLU 11;ASP 20 | mutant V131M | ||||||||
1dygA | GLU 11;ASP 20 | mutant V131E | ||||||||
1epyA | GLU 11;ASP 20 | mutant T21H, C54T, C97A, Q141H, T142H | ||||||||
1l00A | GLU 11;ASP 20 | mutant Q105A | ||||||||
1l01A | GLU 11;ASP 20 | mutant T155A, T157I | ||||||||
1l02A | GLU 11;ASP 20 | mutant T157A | ||||||||
1l03A | GLU 11;ASP 20 | mutant T157C | ||||||||
1l04A | GLU 11;ASP 20 | mutant T157D | ||||||||
1l05A | GLU 11;ASP 20 | mutant T157D | ||||||||
1l06A | GLU 11;ASP 20 | mutant T157E | ||||||||
1l07A | GLU 11;ASP 20 | mutant T157F | ||||||||
1l08A | GLU 11;ASP 20 | mutant T157G | ||||||||
1l09A | GLU 11;ASP 20 | mutant T157H | ||||||||
1l10A | GLU 11;ASP 20 | mutant T157I | ||||||||
1l11A | GLU 11;ASP 20 | mutant T157I | ||||||||
1l12A | GLU 11;ASP 20 | mutant T157N | ||||||||
1l13A | GLU 11;ASP 20 | mutant T157R | ||||||||
1l14A | GLU 11;ASP 20 | mutant T157S | ||||||||
1l15A | GLU 11;ASP 20 | mutant T157V | ||||||||
1l16A | GLU 11;ASP 20 | mutant G156D | ||||||||
1l17A | GLU 11;ASP 20 | mutant I3V | ||||||||
1l18A | GLU 11;ASP 20 | mutant I3Y | ||||||||
1l19A | GLU 11;ASP 20 | mutant S38D | ||||||||
1l20A | GLU 11;ASP 20 | mutant N144D | ||||||||
1l21A | GLU 11;ASP 20 | mutant N55G | ||||||||
1l22A | GLU 11;ASP 20 | mutant K124G | ||||||||
1l23A | GLU 11;ASP 20 | mutant G77A | ||||||||
1l24A | GLU 11;ASP 20 | mutant A82P | ||||||||
1l25A | GLU 11;ASP 20 | mutant P86A | ||||||||
1l26A | GLU 11;ASP 20 | mutant P86C | ||||||||
1l27A | GLU 11;ASP 20 | mutant P86D | ||||||||
1l28A | GLU 11;ASP 20 | mutant P86G | ||||||||
1l29A | GLU 11;ASP 20 | mutant P86H | ||||||||
1l30A | GLU 11;ASP 20 | mutant P86L | ||||||||
1l31A | GLU 11;ASP 20 | mutant P86R | ||||||||
1l32A | GLU 11;ASP 20 | mutant P86S | ||||||||
1l33A | GLU 11;ASP 20 | mutant V131A | ||||||||
1l34A | GLU 11;ASP 20 | mutant R96H | ||||||||
1l35A | GLU 11;ASP 20 | mutant I3Y, I9C, C54T, C97A, L164C | ||||||||
1l36A | GLU 11;ASP 20 | mutant E128A, V131A, N132A | ||||||||
1l37A | GLU 11;ASP 20 | mutant T115E | ||||||||
1l38A | GLU 11;ASP 20 | mutant Q123E | ||||||||
1l39A | GLU 11;ASP 20 | mutant C54T, C97A, N144E | ||||||||
1l40A | GLU 11;ASP 20 | mutant C54T, C97A, N144E | ||||||||
1l41A | GLU 11;ASP 20 | mutant C54T, K83H, C97A, A112D | ||||||||
1l42A | GLU 11;ASP 20 | mutant K16E | ||||||||
1l43A | GLU 11;ASP 20 | mutant K16E | ||||||||
1l44A | GLU 11;ASP 20 | mutant R119E | ||||||||
1l45A | GLU 11;ASP 20 | mutant K135E | ||||||||
1l46A | GLU 11;ASP 20 | mutant K147E | ||||||||
1l47A | GLU 11;ASP 20 | mutant R154E | ||||||||
1l48A | GLU 11;ASP 20 | mutant A98V | ||||||||
1l49A | GLU 11;ASP 20 | mutant A98V, T152S | ||||||||
1l50A | GLU 11;ASP 20 | mutant A98V, V149C, T152S | ||||||||
1l51A | GLU 11;ASP 20 | mutant A98V, V149I, T152S | ||||||||
1l52A | GLU 11;ASP 20 | mutant T152S | ||||||||
1l53A | GLU 11;ASP 20 | mutant V149C | ||||||||
1l54A | GLU 11;ASP 20 | mutant C54T, C97A, M102K | ||||||||
1l55A | GLU 11;ASP 20 | mutant C54T, D92N, C97A | ||||||||
1l56A | GLU 11;ASP 20 | mutant K60P | ||||||||
1l57A | GLU 11;ASP 20 | mutant N116D | ||||||||
1l58A | GLU 11;ASP 20 | mutant P143A | ||||||||
1l59A | GLU 11;ASP 20 | mutant C54T, C97A, T109N | ||||||||
1l60A | GLU 11;ASP 20 | mutant G113A | ||||||||
1l61A | GLU 11;ASP 20 | mutant S38N, C54T, C97A | ||||||||
1l62A | GLU 11;ASP 20 | mutant C54T, C97A, T109D | ||||||||
1l63A | GLU 11;ASP 20 | mutant C54T, C97A | ||||||||
1l64A | GLU 11;ASP 20 | mutant N40A, K43A, S44A, E45A, L46A, D47A, K48A, C54T, C97A | ||||||||
1l65A | GLU 11;ASP 20 | mutant D47A, C54T, C97A | ||||||||
1l66A | GLU 11;ASP 20 | mutant K43A, C54T, C97A | ||||||||
1l67A | GLU 11;ASP 20 | mutant L46A, C54T, C97A | ||||||||
1l68A | GLU 11;ASP 20 | mutant S44A, C54T, C97A | ||||||||
1l69A | GLU 11;ASP 20 | mutant L133A | ||||||||
1l70A | GLU 11;ASP 20 | mutant V131A, N132A | ||||||||
1l71A | GLU 11;ASP 20 | mutant E128A, V131A | ||||||||
1l72A | GLU 11;ASP 20 | mutant D127A, E128A | ||||||||
1l73A | GLU 11;ASP 20 | mutant D127A, E128A, V131A, N132A | ||||||||
1l74A | GLU 11;ASP 20 | mutant E128A, V131A, N132A, L133A | ||||||||
1l75A | GLU 11;ASP 20 | mutant D127A, E128A, V131A, N132A, L133A | ||||||||
1l76A | GLU 11;ASP 20 | mutant C54T, D72P, C97A | ||||||||
1l77A | GLU 11;ASP 20 | mutant C54T, C97A, M102L | ||||||||
1l79A | GLU 11;ASP 20 | mutant C54T, C97A, L99F, V111I | ||||||||
1l80A | GLU 11;ASP 20 | mutant C54T, C97A, L99F, M102L, V111I | ||||||||
1l81A | GLU 11;ASP 20 | mutant C54T, C97A, L99F, M102L, F153L | ||||||||
1l82A | GLU 11;ASP 20 | mutant C54T, C97A, L99F, M102L, V111I, F153L | ||||||||
1l83A | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1l84A | GLU 11;ASP 20 | mutant C54T, C97A, L99A, F153A | ||||||||
1l85A | GLU 11;ASP 20 | mutant C54T, C97A, F153A | ||||||||
1l86A | GLU 11;ASP 20 | mutant C54T, C97A, F153I | ||||||||
1l87A | GLU 11;ASP 20 | mutant C54T, C97A, F153L | ||||||||
1l88A | GLU 11;ASP 20 | mutant C54T, C97A, F153M | ||||||||
1l89A | GLU 11;ASP 20 | mutant C54T, C97A, L99A, F153A | ||||||||
1l90A | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1l91A | GLU 11;ASP 20 | mutant C54T, C97A, L99F | ||||||||
1l92A | GLU 11;ASP 20 | mutant C54T, C97A, L99I | ||||||||
1l93A | GLU 11;ASP 20 | mutant C54T, C97A, L99M | ||||||||
1l94A | GLU 11;ASP 20 | mutant C54T, C97A, L99V | ||||||||
1l95A | GLU 11;ASP 20 | mutant C54T, C97A, F153V | ||||||||
1l96A | GLU 11;ASP 20 | mutant I3P | ||||||||
1l97A | GLU 11;ASP 20 | mutant I3P | ||||||||
1l97B | GLU 11;ASP 20 | mutant I3P | ||||||||
1l98A | GLU 11;ASP 20 | mutant Q105E | ||||||||
1l99A | GLU 11;ASP 20 | mutant Q105G | ||||||||
1lydA | GLU 11;ASP 20 | mutant | ||||||||
1lyeA | GLU 11;ASP 20 | mutant C54T, T59V, C97A | ||||||||
1lyfA | GLU 11;ASP 20 | mutant C54T, T59S, C97A | ||||||||
1lygA | GLU 11;ASP 20 | mutant C54T, T59N, C97A | ||||||||
1lyhA | GLU 11;ASP 20 | mutant C54T, T59G, C97A | ||||||||
1lyiA | GLU 11;ASP 20 | mutant C54T, T59D, C97A | ||||||||
1lyjA | GLU 11;ASP 20 | mutant C54T, T59A, C97A | ||||||||
1nhbA | GLU 11;ASP 20 | mutant C54T, C97A, L99A | ||||||||
1qs5A | GLU 11;ASP 20 | |||||||||
1qs9A | GLU 11;ASP 20 | |||||||||
1qsbA | GLU 11;ASP 20 | |||||||||
1qsqA | GLU 11;ASP 20 | |||||||||
1qt3A | GLU 11;ASP 20 | mutant T26D, C54T, C97A | ||||||||
1qt4A | GLU 11;ASP 20 | mutant T26Q, C54T, C97A | ||||||||
1qt5A | GLU 11; | mutant D20E, C54T, C97A | ||||||||
1qt6A | ;ASP 20 | mutant E11H, C54T, C97A | ||||||||
1qt7A | ;ASP 20 | mutant E11N, C54T, C97A | ||||||||
1qt8A | GLU 11;ASP 20 | mutant T26H, C54T, C97A | ||||||||
1qtbA | GLU 11;ASP 20 | |||||||||
1qtcA | GLU 11;ASP 20 | |||||||||
1qtdA | GLU 11;ASP 20 | |||||||||
1qthA | GLU 11;ASP 20 | |||||||||
1qthB | GLU 11;ASP 20 | |||||||||
1qtvA | GLU 11;ASP 20 | mutant T26E, C54T, C97A | ||||||||
1qtzA | GLU 11; | mutant D20C, C54T, C97A | ||||||||
1qudA | GLU 11;ASP 20 | mutant L99G | ||||||||
1qugA | GLU 11;ASP 20 | mutant E108V | ||||||||
1quhA | GLU 11;ASP 20 | mutant L99G, E108V | ||||||||
1quoA | GLU 11;ASP 20 | mutant L99A, E108V | ||||||||
1tlaA | GLU 11;ASP 20 | mutant C54T, C97A, S117F | ||||||||
200lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A | ||||||||
201lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion K48-HP | ||||||||
201lB | GLU 11;ASP 20 | mutant C54T, C97A, insertion K48-HP | ||||||||
205lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion S44-AAA | ||||||||
206lA | GLU 11;ASP 20 | mutant A42S, C54T, C97A | ||||||||
209lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion A73-AAA | ||||||||
210lA | GLU 11;ASP 20 | mutant C54T, C97A, deletion A73 | ||||||||
211lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion E108-A | ||||||||
212lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion L164-AAAA | ||||||||
213lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion N140-A | ||||||||
214lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion R119-A | ||||||||
215lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion T115-A | ||||||||
216lA | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
216lB | GLU 11;ASP 20 | mutant S44W, C54T, C97A | ||||||||
217lA | GLU 11;ASP 20 | mutant S44E, C54T, C97A | ||||||||
218lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion V131-A | ||||||||
219lA | GLU 11;ASP 20 | mutant C54T, C97A, insertion L164-AAAA | ||||||||
220lA | GLU 11;ASP 20 | mutant C54T, C97A, M102A | ||||||||
221lA | GLU 11;ASP 20 | mutant A49S, C54T, C97A | ||||||||
222lA | GLU 11;ASP 20 | mutant C54T, C97A, M102A | ||||||||
223lA | GLU 11;ASP 20 | mutant L133G | ||||||||
224lA | GLU 11;ASP 20 | mutant C54T, A93S, C97A | ||||||||
225lA | GLU 11;ASP 20 | mutant L133G | ||||||||
226lA | GLU 11;ASP 20 | mutant L133G | ||||||||
227lA | GLU 11;ASP 20 | mutant C54T, C97A, F104A | ||||||||
228lA | GLU 11;ASP 20 | mutant C54T, C97A, F104A | ||||||||
229lA | GLU 11;ASP 20 | mutant C54T, R95A, C97A | ||||||||
230lA | GLU 11;ASP 20 | mutant M6L, C54T, C97A | ||||||||
231lA | GLU 11;ASP 20 | mutant C54T, C97A, M106K | ||||||||
232lA | GLU 11;ASP 20 | mutant C54T, C97A, M120K | ||||||||
233lA | GLU 11;ASP 20 | mutant C54T, C97A, M120L | ||||||||
234lA | GLU 11;ASP 20 | mutant C54T, C97A, M106L | ||||||||
235lA | GLU 11;ASP 20 | mutant C54T, C97A, V111A | ||||||||
236lA | GLU 11;ASP 20 | mutant C54T, V87A, C97A | ||||||||
237lA | GLU 11;ASP 20 | mutant C54T, C97A, V149A | ||||||||
238lA | GLU 11;ASP 20 | mutant C54T, C97A, V103A | ||||||||
239lA | GLU 11;ASP 20 | mutant I17A, C54T, C97A | ||||||||
240lA | GLU 11;ASP 20 | mutant I27A, C54T, C97A | ||||||||
241lA | GLU 11;ASP 20 | mutant I29A, C54T, C97A | ||||||||
242lA | GLU 11;ASP 20 | mutant I50A, C54T, C97A | ||||||||
243lA | GLU 11;ASP 20 | mutant C54T, I58A, C97A | ||||||||
244lA | GLU 11;ASP 20 | mutant C54T, C97A, I100A | ||||||||
245lA | GLU 11;ASP 20 | mutant M6A, C54T, C97A | ||||||||
246lA | GLU 11;ASP 20 | mutant C54T, F67A, C97A | ||||||||
247lA | GLU 11;ASP 20 | mutant C54T, L84A, C97A | ||||||||
248lA | GLU 11;ASP 20 | mutant I27A, I29A, C54T, C97A | ||||||||
249lA | GLU 11;ASP 20 | mutant I27A, C54T, I58A, C97A | ||||||||
250lA | GLU 11;ASP 20 | mutant I29A, C54T, I58A, C97A | ||||||||
251lA | GLU 11;ASP 20 | mutant C54T, C97A, L121A, L133A | ||||||||
252lA | GLU 11;ASP 20 | mutant C54T, C97A, M102A, M106A | ||||||||
253lA | GLU 11; | mutant D20A, C54T, C97A | ||||||||
254lA | GLU 11; | mutant D20S, C54T, C97A | ||||||||
255lA | GLU 11; | mutant D20N, C54T, C97A | ||||||||
256lA | GLU 11;ASP 20 | mutant M6I | ||||||||
257lA | GLU 11;ASP 20 | mutant C54T, C97A | ||||||||
258lA | GLU 11;ASP 20 | mutant | ||||||||
259lA | GLU 11;ASP 20 | mutant T21H, C54T, C97A, T142H | ||||||||
260lA | GLU 11;ASP 20 | mutant T21H, C54T, C97A, T142H | ||||||||
262lA | GLU 11;ASP 20 | mutant L39I, insertion I50-NAAKSELDKAI | ||||||||
262lB | GLU 11;ASP 20 | mutant L39I, insertion I50-NAAKSELDKAI | ||||||||
2l78A | GLU 11;ASP 20 | mutant C54T, C97A, V111I | ||||||||
2lzmA | GLU 11;ASP 20 | mutant | ||||||||
3lzmA | GLU 11;ASP 20 | mutant | ||||||||
4lzmA | GLU 11;ASP 20 | mutant | ||||||||
5lzmA | GLU 11;ASP 20 | mutant | ||||||||
6lzmA | GLU 11;ASP 20 | mutant | ||||||||
7lzmA | GLU 11;ASP 20 | mutant |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[3]
|
||
[4]
|
||
[24]
|
Fig.1, p.9461-9463 | 2 |
[50]
|
Fig.3 | |
[52]
|
p.6787 | |
[59]
|
||
[61]
|
Fig.3, p.1007 | |
[64]
|
Fig.2, p.58 | |
[77]
|
Fig.4, p.8951-8953 |
References | |
---|---|
[1] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.4 ANGSTROMS). |
Medline ID | 77157239 |
PubMed ID | 322662 |
Journal | Biochem Biophys Res Commun |
Year | 1977 |
Volume | 75 |
Pages | 265-70 |
Authors | Remington SJ, Eyck LF, Matthews BW |
Title | Atomic coordinates for T4 phage lysozyme. |
Related PDB | |
Related UniProtKB | P00720 |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7308203 |
Journal | Eur J Biochem |
Year | 1981 |
Volume | 119 |
Pages | 589-93 |
Authors | Kleppe G, Vasstrand E, Jensen HB |
Title |
The specificity requirements of bacteriophage T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7277499 |
Journal | J Mol Biol |
Year | 1981 |
Volume | 147 |
Pages | 523-43 |
Authors | Anderson WF, Grutter MG, Remington SJ, Weaver LH, Matthews BW |
Title | Crystallographic determination of the mode of binding of oligosaccharides to T4 bacteriophage lysozyme: implications for the mechanism of catalysis. |
Related PDB | |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7207627 |
Journal | Nature |
Year | 1981 |
Volume | 290 |
Pages | 334-5 |
Authors | Matthews BW, Grutter MG, Anderson WF, Remington SJ |
Title | Common precursor of lysozymes of hen egg-white and bacteriophage T4. |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7077670 |
Journal | J Mol Biol |
Year | 1982 |
Volume | 154 |
Pages | 525-35 |
Authors | Grutter MG, Matthews BW |
Title | Amino acid substitutions far from the active site of bacteriophage T4 lysozyme reduce catalytic activity and suggest that the C-terminal lobe of the enzyme participates in substrate binding. |
Related PDB | |
Related UniProtKB | |
[6] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3680274 |
Journal | J Biol Chem |
Year | 1987 |
Volume | 262 |
Pages | 16858-64 |
Authors | Gray TM, Matthews BW |
Title |
Structural analysis of the temperature-sensitive mutant of bacteriophage T4 lysozyme, |
Related PDB | 1l16 |
Related UniProtKB | |
[7] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3681997 |
Journal | J Mol Biol |
Year | 1987 |
Volume | 197 |
Pages | 315-29 |
Authors | Grutter MG, Gray TM, Weaver LH, Wilson TA, Matthews BW |
Title |
Structural studies of mutants of the lysozyme of bacteriophage T4. |
Related PDB | 1l01 1l10 |
Related UniProtKB | |
[8] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.7 ANGSTROMS). |
Medline ID | 87226186 |
PubMed ID | 3586019 |
Journal | J Mol Biol |
Year | 1987 |
Volume | 193 |
Pages | 189-99 |
Authors | Weaver LH, Matthews BW |
Title | Structure of bacteriophage T4 lysozyme refined at 1.7 A resolution. |
Related PDB | 2lzm |
Related UniProtKB | P00720 |
[9] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3118211 |
Journal | Nature |
Year | 1987 |
Volume | 330 |
Pages | 41-6 |
Authors | Alber T, Sun DP, Wilson K, Wozniak JA, Cook SP, Matthews BW |
Title | Contributions of hydrogen bonds of Thr 157 to the thermodynamic stability of phage T4 lysozyme. |
Related PDB | 1l02 1l03 1l04 1l05 1l06 1l07 1l08 1l09 1l11 1l12 1l13 1l14 1l15 1l14 |
Related UniProtKB | |
[10] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3477797 |
Journal | Proc Natl Acad Sci U S A |
Year | 1987 |
Volume | 84 |
Pages | 6663-7 |
Authors | Matthews BW, Nicholson H, Becktel WJ |
Title | Enhanced protein thermostability from site-directed mutations that decrease the entropy of unfolding. |
Related PDB | 1l23 1l24 |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 3029773 |
Journal | Proc Natl Acad Sci U S A |
Year | 1987 |
Volume | 84 |
Pages | 1244-8 |
Authors | McIntosh LP, Griffey RH, Muchmore DC, Nielson CP, Redfield AG, Dahlquist FW |
Title | Proton NMR measurements of bacteriophage T4 lysozyme aided by 15N isotopic labeling: structural and dynamic studies of larger proteins. |
Related PDB | |
Related UniProtKB | |
[12] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.7 ANGSTROMS) OF MUTANT ILE-3. |
Medline ID | 88302415 |
PubMed ID | 3405287 |
Journal | Nature |
Year | 1988 |
Volume | 334 |
Pages | 406-10 |
Authors | Matsumura M, Becktel WJ, Matthews BW |
Title | Hydrophobic stabilization in T4 lysozyme determined directly by multiple substitutions of Ile 3. |
Related PDB | 1l17 1l18 |
Related UniProtKB | P00720 |
[13] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3200317 |
Journal | Nature |
Year | 1988 |
Volume | 336 |
Pages | 651-6 |
Authors | Nicholson H, Becktel WJ, Matthews BW |
Title | Enhanced protein thermostability from designed mutations that interact with alpha-helix dipoles. |
Related PDB | 1l19 1l20 |
Related UniProtKB | |
[14] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3074306 |
Journal | Protein Eng |
Year | 1988 |
Volume | 2 |
Pages | 277-82 |
Authors | Rose DR, Phipps J, Michniewicz J, Birnbaum GI, Ahmed FR, Muir A, Anderson WF, Narang S |
Title | Crystal structure of T4-lysozyme generated from synthetic coding DNA expressed in Escherichia coli. |
Related PDB | 1lyd |
Related UniProtKB | |
[15] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 3277275 |
Journal | Science |
Year | 1988 |
Volume | 239 |
Pages | 631-5 |
Authors | Alber T, Bell JA, Sun DP, Nicholson H, Wozniak JA, Cook S, Matthews BW |
Title | Replacements of Pro86 in phage T4 lysozyme extend an alpha-helix but do not alter protein stability. |
Related PDB | 1l25 1l26 1l27 1l28 1l29 1l30 1l31 1l32 |
Related UniProtKB | |
[16] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2665808 |
Journal | Biochemistry |
Year | 1989 |
Volume | 28 |
Pages | 3793-7 |
Authors | Weaver LH, Gray TM, Grutter MG, Anderson DE, Wozniak JA, Dahlquist FW, Matthews BW |
Title |
High-resolution structure of the temperature-sensitive mutant of phage lysozyme, |
Related PDB | 1l34 |
Related UniProtKB | |
[17] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2674124 |
Journal | J Biol Chem |
Year | 1989 |
Volume | 264 |
Pages | 16059-66 |
Authors | Matsumura M, Wozniak JA, Sun DP, Matthews BW |
Title | Structural studies of mutants of T4 lysozyme that alter hydrophobic stabilization. |
Related PDB | 3lzm |
Related UniProtKB | |
[18] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2511328 |
Journal | J Mol Biol |
Year | 1989 |
Volume | 210 |
Pages | 181-93 |
Authors | Nicholson H, Soderlind E, Tronrud DE, Matthews BW |
Title | Contributions of left-handed helical residues to the structure and stability of bacteriophage T4 lysozyme. |
Related PDB | 1l21 1l22 1l33 |
Related UniProtKB | |
[19] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2916125 |
Journal | Science |
Year | 1989 |
Volume | 243 |
Pages | 792-4 |
Authors | Matsumura M, Matthews BW |
Title | Control of enzyme activity by an engineered disulfide bond. |
Related PDB | 155l 156l 157l 158l 159l 160l 161l 162l 163l 164l 165l 166l |
Related UniProtKB | |
[20] | |
Resource | |
Comments | STRUCTURE BY NMR. |
Medline ID | 91002526 |
PubMed ID | 2207079 |
Journal | Biochemistry |
Year | 1990 |
Volume | 29 |
Pages | 6341-62 |
Authors | McIntosh LP, Wand AJ, Lowry DF, Redfield AG, Dahlquist FW |
Title | Assignment of the backbone 1H and 15N NMR resonances of bacteriophage T4 lysozyme. |
Related PDB | |
Related UniProtKB | P00720 |
[21] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2334683 |
Journal | Biochemistry |
Year | 1990 |
Volume | 29 |
Pages | 2592-8 |
Authors | Pjura PE, Matsumura M, Wozniak JA, Matthews BW |
Title | Structure of a thermostable disulfide-bridge mutant of phage T4 lysozyme shows that an engineered cross-link in a flexible region does not increase the rigidity of the folded protein. |
Related PDB | 1l35 |
Related UniProtKB | |
[22] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.8 ANGSTROMS) OF MUTANT. |
Medline ID | 91043097 |
PubMed ID | 2234094 |
Journal | Nature |
Year | 1990 |
Volume | 348 |
Pages | 263-6 |
Authors | Faber HR, Matthews BW |
Title | A mutant T4 lysozyme displays five different crystal conformations. |
Related PDB | 256l |
Related UniProtKB | P00720 |
[23] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1747370 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 11521-9 |
Authors | Dao-pin S, Anderson DE, Baase WA, Dahlquist FW, Matthews BW |
Title | Structural and thermodynamic consequences of burying a charged residue within the hydrophobic core of T4 lysozyme. |
Related PDB | 1l54 |
Related UniProtKB | |
[24] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1892846 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 9457-63 |
Authors | Hardy LW, Poteete AR |
Title | Reexamination of the role of Asp20 in catalysis by bacteriophage T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[25] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1911773 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 9816-28 |
Authors | Nicholson H, Anderson DE, Dao-pin S, Matthews BW |
Title | Analysis of the interaction between charged side chains and the alpha-helix dipole using designed thermostable mutants of phage T4 lysozyme. |
Related PDB | 1l55 1l57 1l59 1l61 1l62 1l63 |
Related UniProtKB | |
[26] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1991123 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 1425-32 |
Authors | Poteete AR, Sun DP, Nicholson H, Matthews BW |
Title | Second-site revertants of an inactive T4 lysozyme mutant restore activity by restructuring the active site cleft. |
Related PDB | |
Related UniProtKB | |
[27] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1854726 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 7142-53 |
Authors | Sun DP, Sauer U, Nicholson H, Matthews BW |
Title | Contributions of engineered surface salt bridges to the stability of T4 lysozyme determined by directed mutagenesis. |
Related PDB | 1l37 1l38 1l39 1l40 1l41 |
Related UniProtKB | |
[28] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1998663 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 2012-7 |
Authors | Zhang XJ, Baase WA, Matthews BW |
Title | Toward a simplification of the protein folding problem: a stabilizing polyalanine alpha-helix engineered in T4 lysozyme. |
Related PDB | 1l36 |
Related UniProtKB | |
[29] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1814699 |
Journal | Ciba Found Symp |
Year | 1991 |
Volume | 161 |
Pages | 91-103; discussion 103-7 |
Authors | Kollman PA, Daggett V, Dang LX |
Title | The application of computational methods to the study of enzyme catalysis by triose-phosphate isomerase and stabilities of variants of bacteriophage T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[30] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1920439 |
Journal | J Mol Biol |
Year | 1991 |
Volume | 221 |
Pages | 647-67 |
Authors | Daopin S, Alber T, Baase WA, Wozniak JA, Matthews BW |
Title | Structural and thermodynamic analysis of the packing of two alpha-helices in bacteriophage T4 lysozyme. |
Related PDB | 1l48 1l49 1l50 1l51 1l52 1l53 |
Related UniProtKB | |
[31] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1942034 |
Journal | J Mol Biol |
Year | 1991 |
Volume | 221 |
Pages | 873-87 |
Authors | Sun DP, Soderlind E, Baase WA, Wozniak JA, Sauer U, Matthews BW |
Title | Cumulative site-directed charge-change replacements in bacteriophage T4 lysozyme suggest that long-range electrostatic interactions contribute little to protein stability. |
Related PDB | 1l42 1l43 1l44 1l45 1l46 1l47 1l58 |
Related UniProtKB | |
[32] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 2062826 |
Journal | Proteins |
Year | 1991 |
Volume | 10 |
Pages | 10-21 |
Authors | Bell JA, Wilson KP, Zhang XJ, Faber HR, Nicholson H, Matthews BW |
Title |
Comparison of the crystal structure of bacteriophage T4 lysozyme at low, |
Related PDB | 4lzm 5lzm 6lzm 7lzm |
Related UniProtKB | |
[33] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1567817 |
Journal | Biochemistry |
Year | 1992 |
Volume | 31 |
Pages | 3590-6 |
Authors | Bell JA, Becktel WJ, Sauer U, Baase WA, Matthews BW |
Title | Dissection of helix capping in T4 lysozyme by structural and thermodynamic analysis of six amino acid substitutions at Thr 59. |
Related PDB | 1lye 1lyf 1lyg 1lyh 1lyi 1lyj |
Related UniProtKB | |
[34] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1457724 |
Journal | Biopolymers |
Year | 1992 |
Volume | 32 |
Pages | 1431-41 |
Authors | Nicholson H, Tronrud DE, Becktel WJ, Matthews BW |
Title | Analysis of the effectiveness of proline substitutions and glycine replacements in increasing the stability of phage T4 lysozyme. |
Related PDB | 1l56 1l60 |
Related UniProtKB | |
[35] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1733941 |
Journal | J Biol Chem |
Year | 1992 |
Volume | 267 |
Pages | 2393-9 |
Authors | Sauer UH, San DP, Matthews BW |
Title | Tolerance of T4 lysozyme to proline substitutions within the long interdomain alpha-helix illustrates the adaptability of proteins to potentially destabilizing lesions. |
Related PDB | 1l76 |
Related UniProtKB | |
[36] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1404394 |
Journal | J Mol Biol |
Year | 1992 |
Volume | 227 |
Pages | 917-33 |
Authors | Dixon MM, Nicholson H, Shewchuk L, Baase WA, Matthews BW |
Title |
Structure of a hinge-bending bacteriophage T4 lysozyme mutant, |
Related PDB | 1l96 1l97 |
Related UniProtKB | |
[37] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1569571 |
Journal | J Mol Biol |
Year | 1992 |
Volume | 224 |
Pages | 1143-59 |
Authors | Hurley JH, Baase WA, Matthews BW |
Title | Design and structural analysis of alternative hydrophobic core packing arrangements in bacteriophage T4 lysozyme. |
Related PDB | 1l77 1l79 1l80 1l81 1l82 2l78 |
Related UniProtKB | |
[38] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY OF MUTANT. |
Medline ID | 92115004 |
PubMed ID | 1731252 |
Journal | Nature |
Year | 1992 |
Volume | 355 |
Pages | 371-3 |
Authors | Eriksson AE, Baase WA, Wozniak JA, Matthews BW |
Title | A cavity-containing mutant of T4 lysozyme is stabilized by buried benzene. |
Related PDB | 1l83 1l84 |
Related UniProtKB | P00720 |
[39] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1570293 |
Journal | Proc Natl Acad Sci U S A |
Year | 1992 |
Volume | 89 |
Pages | 3751-5 |
Authors | Heinz DW, Baase WA, Matthews BW |
Title | Folding and function of a T4 lysozyme containing 10 consecutive alanines illustrate the redundancy of information in an amino acid sequence. |
Related PDB | 1l64 1l65 1l66 1l67 1l68 |
Related UniProtKB | |
[40] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1304882 |
Journal | Protein Sci |
Year | 1992 |
Volume | 1 |
Pages | 46-57 |
Authors | Jacobson RH, Matsumura M, Faber HR, Matthews BW |
Title | Structure of a stabilizing disulfide bridge mutant that closes the active-site cleft of T4 lysozyme. |
Related PDB | 259l 1kni |
Related UniProtKB | |
[41] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 1304917 |
Journal | Protein Sci |
Year | 1992 |
Volume | 1 |
Pages | 761-76 |
Authors | Zhang XJ, Baase WA, Matthews BW |
Title |
Multiple alanine replacements within alpha-helix 126-134 of T4 lysozyme have independent, |
Related PDB | 1l69 1l70 1l71 1l72 1l73 1l74 1l75 |
Related UniProtKB | |
[42] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8218201 |
Journal | Biochemistry |
Year | 1993 |
Volume | 32 |
Pages | 11363-73 |
Authors | Blaber M, Lindstrom JD, Gassner N, Xu J, Heinz DW, Matthews BW |
Title | Energetic cost and structural consequences of burying a hydroxyl group within the core of a protein determined from Ala-->Ser and Val-->Thr substitutions in T4 lysozyme. |
Related PDB | 118l 119l 120l 122l 123l 125l 126l 127l 128l 206l 221l 224l |
Related UniProtKB | |
[43] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8433369 |
Journal | J Mol Biol |
Year | 1993 |
Volume | 229 |
Pages | 747-69 |
Authors | Eriksson AE, Baase WA, Matthews BW |
Title | Similar hydrophobic replacements of Leu99 and Phe153 within the core of T4 lysozyme have different structural and thermodynamic consequences. |
Related PDB | 1l85 1l86 1l87 1l88 1l89 1l90 1l91 1l92 1l93 1l94 1l95 |
Related UniProtKB | |
[44] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8429913 |
Journal | Nature |
Year | 1993 |
Volume | 361 |
Pages | 561-4 |
Authors | Heinz DW, Baase WA, Dahlquist FW, Matthews BW |
Title | How amino-acid insertions are allowed in an alpha-helix of T4 lysozyme. |
Related PDB | 102l 103l 104l 201l 205l |
Related UniProtKB | |
[45] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8401213 |
Journal | Protein Sci |
Year | 1993 |
Volume | 2 |
Pages | 1285-90 |
Authors | Anderson DE, Hurley JH, Nicholson H, Baase WA, Matthews BW |
Title | Hydrophobic core repacking and aromatic-aromatic interaction in the thermostable mutant of T4 lysozyme Ser 117-->Phe. |
Related PDB | 1tla |
Related UniProtKB | |
[46] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8298466 |
Journal | Protein Sci |
Year | 1993 |
Volume | 2 |
Pages | 2226-32 |
Authors | Pjura P, Matthews BW |
Title | Structures of randomly generated mutants of T4 lysozyme show that protein stability can be enhanced by relaxation of strain and by improved hydrogen bonding via bound solvent. |
Related PDB | 129l 130l 131l |
Related UniProtKB | |
[47] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8460110 |
Journal | Proteins |
Year | 1993 |
Volume | 15 |
Pages | 401-12 |
Authors | Pjura P, McIntosh LP, Wozniak JA, Matthews BW |
Title |
Perturbation of Trp 138 in T4 lysozyme by mutations at Gln 105 used to correlate changes in structure, |
Related PDB | 1l00 1l98 1l99 |
Related UniProtKB | |
[48] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8259514 |
Journal | Science |
Year | 1993 |
Volume | 262 |
Pages | 1715-8 |
Authors | Baldwin EP, Hajiseyedjavadi O, Baase WA, Matthews BW |
Title | The role of backbone flexibility in the accommodation of variants that repack the core of T4 lysozyme. |
Related PDB | 140l 141l 142l 143l 144l 145l 146l 147l |
Related UniProtKB | |
[49] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8503008 |
Journal | Science |
Year | 1993 |
Volume | 260 |
Pages | 1637-40 |
Authors | Blaber M, Zhang XJ, Matthews BW |
Title | Structural basis of amino acid alpha helix propensity. |
Related PDB | 107l 108l 109l 110l 111l 112l 113l 114l 115l 116l 137l 216l 217l |
Related UniProtKB | |
[50] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8266098 |
Journal | Science |
Year | 1993 |
Volume | 262 |
Pages | 2030-3 |
Authors | Kuroki R, Weaver LH, Matthews BW |
Title | A covalent enzyme-substrate intermediate with saccharide distortion in a mutant T4 lysozyme. |
Related PDB | 148l |
Related UniProtKB | |
[51] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7727368 |
Journal | Biochemistry |
Year | 1994 |
Volume | 33 |
Pages | 11174-83 |
Authors | McLeish MJ, Nielsen KJ, Najbar LV, Wade JD, Lin F, Doughty MB, Craik DJ |
Title | Conformation of a peptide corresponding to T4 lysozyme residues 59-81 by NMR and CD spectroscopy. |
Related PDB | |
Related UniProtKB | |
[52] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7961435 |
Journal | J Bacteriol |
Year | 1994 |
Volume | 176 |
Pages | 6783-8 |
Authors | Poteete AR, Hardy LW |
Title | Genetic analysis of bacteriophage T4 lysozyme structure and function. |
Related PDB | |
Related UniProtKB | |
[53] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8289284 |
Journal | J Mol Biol |
Year | 1994 |
Volume | 235 |
Pages | 600-24 |
Authors | Blaber M, Zhang XJ, Lindstrom JD, Pepiot SD, Baase WA, Matthews BW |
Title |
Determination of alpha-helix propensity within the context of a folded protein. |
Related PDB | 1dya 1dyb 1dyc 1dyd 1dye 1dyf 1dyg |
Related UniProtKB | |
[54] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8114100 |
Journal | J Mol Biol |
Year | 1994 |
Volume | 236 |
Pages | 869-86 |
Authors | Heinz DW, Baase WA, Zhang XJ, Blaber M, Dahlquist FW, Matthews BW |
Title |
Accommodation of amino acid insertions in an alpha-helix of T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[55] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8177878 |
Journal | Protein Eng |
Year | 1994 |
Volume | 7 |
Pages | 301-7 |
Authors | Heinz DW, Matthews BW |
Title | Rapid crystallization of T4 lysozyme by intermolecular disulfide cross-linking. |
Related PDB | 138l 139l |
Related UniProtKB | |
[56] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 7920248 |
Journal | Protein Sci |
Year | 1994 |
Volume | 3 |
Pages | 1031-9 |
Authors | Zhang XJ, Matthews BW |
Title | Conservation of solvent-binding sites in 10 crystal forms of T4 lysozyme. |
Related PDB | 149l 150l 151l 152l |
Related UniProtKB | |
[57] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 7612599 |
Journal | Biochemistry |
Year | 1995 |
Volume | 34 |
Pages | 8576-88 |
Authors | Morton A, Matthews BW |
Title | Specificity of ligand binding in a buried nonpolar cavity of T4 lysozyme: linkage of dynamics and structural plasticity. |
Related PDB | 181l 182l 183l 184l 185l 186l 187l 188l 1nhb |
Related UniProtKB | |
[58] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7632721 |
Journal | Biochim Biophys Acta |
Year | 1995 |
Volume | 1250 |
Pages | 163-70 |
Authors | Najbar LV, Craik DJ, Wade JD, Lin F, McLeish MJ |
Title | CD and NMR determination of the solution structure of a peptide corresponding to T4 lysozyme residues 38-51. |
Related PDB | |
Related UniProtKB | |
[59] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7823320 |
Journal | J Mol Biol |
Year | 1995 |
Volume | 245 |
Pages | 54-68 |
Authors | Weaver LH, Grutter MG, Matthews BW |
Title | The refined structures of goose lysozyme and its complex with a bound trisaccharide show that the "goose-type" lysozymes lack a catalytic aspartate residue. |
Related PDB | |
Related UniProtKB | |
[60] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 7616572 |
Journal | J Mol Biol |
Year | 1995 |
Volume | 250 |
Pages | 527-52 |
Authors | Zhang XJ, Wozniak JA, Matthews BW |
Title | Protein flexibility and adaptability seen in 25 crystal forms of T4 lysozyme. |
Related PDB | 167l 168l 169l 170l 171l 172l 173l 174l 175l 176l 177l 178l 179l 180l |
Related UniProtKB | |
[61] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7583653 |
Journal | Nat Struct Biol |
Year | 1995 |
Volume | 2 |
Pages | 1007-11 |
Authors | Kuroki R, Weaver LH, Matthews BW |
Title | Structure-based design of a lysozyme with altered catalytic activity. |
Related PDB | |
Related UniProtKB | |
[62] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 7831309 |
Journal | Proc Natl Acad Sci U S A |
Year | 1995 |
Volume | 92 |
Pages | 452-6 |
Authors | Shoichet BK, Baase WA, Kuroki R, Matthews BW |
Title | A relationship between protein stability and protein function. |
Related PDB | 253l 254l 255l |
Related UniProtKB | |
[63] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8771182 |
Journal | Protein Eng |
Year | 1995 |
Volume | 8 |
Pages | 1017-22 |
Authors | Zhang XJ, Baase WA, Shoichet BK, Wilson KP, Matthews BW |
Title | Enhancement of protein stability by the combination of point mutations in T4 lysozyme is additive. |
Related PDB | 189l |
Related UniProtKB | |
[64] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8958073 |
Journal | Ann N Y Acad Sci |
Year | 1996 |
Volume | 799 |
Pages | 56-60 |
Authors | Morimoto K, Kuroki R, Matthews BW |
Title | Control of the catalytic mechanism of an enzyme by amino acid substitution. |
Related PDB | |
Related UniProtKB | |
[65] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8676387 |
Journal | J Mol Biol |
Year | 1996 |
Volume | 259 |
Pages | 542-59 |
Authors | Baldwin E, Xu J, Hajiseyedjavadi O, Baase WA, Matthews BW |
Title | Thermodynamic and structural compensation in "size-switch" core repacking variants of bacteriophage T4 lysozyme. |
Related PDB | 195l 196l 197l 198l 199l 200l |
Related UniProtKB | |
[66] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 8976549 |
Journal | Protein Sci |
Year | 1996 |
Volume | 5 |
Pages | 2399-415 |
Authors | Vetter IR, Baase WA, Heinz DW, Xiong JP, Snow S, Matthews BW |
Title | Protein structural plasticity exemplified by insertion and deletion mutants in T4 lysozyme. |
Related PDB | 209l 210l 211l 212l 213l 214l 215l 218l 219l |
Related UniProtKB | |
[67] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9003182 |
Journal | Biochemistry |
Year | 1997 |
Volume | 36 |
Pages | 307-16 |
Authors | Mchaourab HS, Oh KJ, Fang CJ, Hubbell WL |
Title |
Conformation of T4 lysozyme in solution. |
Related PDB | |
Related UniProtKB | |
[68] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10099305 |
Journal | Biotechnol Bioeng |
Year | 1998 |
Volume | 58 |
Pages | 658-62 |
Authors | Bower CK, Xu Q, McGuire J |
Title | Activity losses among T4 lysozyme variants after adsorption to colloidal silica. |
Related PDB | |
Related UniProtKB | |
[69] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 9514755 |
Journal | J Mol Biol |
Year | 1998 |
Volume | 277 |
Pages | 467-85 |
Authors | Baldwin E, Baase WA, Zhang X, Feher V, Matthews BW |
Title | Generation of ligand binding sites in T4 lysozyme by deficiency-creating substitutions. |
Related PDB | 220l 222l 223l 225l 226l 227l 228l 229l 252l |
Related UniProtKB | |
[70] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9514719 |
Journal | J Mol Biol |
Year | 1998 |
Volume | 276 |
Pages | 151-64 |
Authors | Evrard C, Fastrez J, Declercq JP |
Title | Crystal structure of the lysozyme from bacteriophage lambda and its relationship with V and C-type lysozymes. |
Related PDB | |
Related UniProtKB | |
[71] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 9541409 |
Journal | Protein Sci |
Year | 1998 |
Volume | 7 |
Pages | 765-73 |
Authors | Lipscomb LA, Gassner NC, Snow SD, Eldridge AM, Baase WA, Drew DL, Matthews BW |
Title | Context-dependent protein stabilization by methionine-to-leucine substitution shown in T4 lysozyme. |
Related PDB | 230l 231l 232l 233l 234l |
Related UniProtKB | |
[72] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 9514271 |
Journal | Protein Sci |
Year | 1998 |
Volume | 7 |
Pages | 158-77 |
Authors | Xu J, Baase WA, Baldwin E, Matthews BW |
Title | The response of T4 lysozyme to large-to-small substitutions within the core and its relation to the hydrophobic effect. |
Related PDB | 235l 236l 237l 238l 239l 240l 241l 242l 243l 244l 245l 246l 247l 248l 249l 250l 251l |
Related UniProtKB | |
[73] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10545167 |
Journal | Biochemistry |
Year | 1999 |
Volume | 38 |
Pages | 14451-60 |
Authors | Gassner NC, Baase WA, Lindstrom JD, Lu J, Dahlquist FW, Matthews BW |
Title | Methionine and alanine substitutions show that the formation of wild-type-like structure in the carboxy-terminal domain of T4 lysozyme is a rate-limiting step in folding. |
Related PDB | 1ctw 1cu0 1cu2 1cu3 1cu5 1cu6 1cup 1cuq 1cv0 1cv1 1cv3 1cv4 1cv5 1cv6 1cvk 1cx7 1qsq |
Related UniProtKB | |
[74] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10074347 |
Journal | Biochemistry |
Year | 1999 |
Volume | 38 |
Pages | 2947-55 |
Authors | Mchaourab HS, Kalai T, Hideg K, Hubbell WL |
Title | Motion of spin-labeled side chains in T4 lysozyme: effect of side chain structure. |
Related PDB | |
Related UniProtKB | |
[75] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10556025 |
Journal | J Mol Biol |
Year | 1999 |
Volume | 294 |
Pages | 17-20 |
Authors | Gassner NC, Baase WA, Hausrath AC, Matthews BW |
Title | Substitution with selenomethionine can enhance the stability of methionine-rich proteins. |
Related PDB | 1cx6 1d2w 1d2y 1d3f 1d3j 1d3m 1d3n |
Related UniProtKB | |
[76] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10512706 |
Journal | J Mol Biol |
Year | 1999 |
Volume | 292 |
Pages | 1111-20 |
Authors | Wray JW, Baase WA, Lindstrom JD, Weaver LH, Poteete AR, Matthews BW |
Title | Structural analysis of a non-contiguous second-site revertant in T4 lysozyme shows that increasing the rigidity of a protein can enhance its stability. |
Related PDB | 1qud 1qug 1quh 1quo |
Related UniProtKB | |
[77] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10430876 |
Journal | Proc Natl Acad Sci U S A |
Year | 1999 |
Volume | 96 |
Pages | 8949-54 |
Authors | Kuroki R, Weaver LH, Matthews BW |
Title | Structural basis of the conversion of T4 lysozyme into a transglycosidase by reengineering the active site. |
Related PDB | 1qt3 1qt4 1qt5 1qt6 1qt7 1qt8 1qtv 1qtz |
Related UniProtKB | |
[78] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10339544 |
Journal | Proc Natl Acad Sci U S A |
Year | 1999 |
Volume | 96 |
Pages | 6078-83 |
Authors | Sagermann M, Baase WA, Matthews BW |
Title | Structural characterization of an engineered tandem repeat contrasts the importance of context and sequence in protein folding. |
Related PDB | 262l 261l |
Related UniProtKB | |
[79] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10623513 |
Journal | J Mol Biol |
Year | 2000 |
Volume | 295 |
Pages | 127-45 |
Authors | Liu R, Baase WA, Matthews BW |
Title | The introduction of strain and its effects on the structure and stability of T4 lysozyme. |
Related PDB | 1qs5 1qs9 1qsb 1qtb 1qtc 1qtd 1qth |
Related UniProtKB | |
[80] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10993735 |
Journal | J Mol Biol |
Year | 2000 |
Volume | 302 |
Pages | 955-77 |
Authors | Quillin ML, Breyer WA, Griswold IJ, Matthews BW |
Title | Size versus polarizability in protein-ligand interactions: binding of noble gases within engineered cavities in phage T4 lysozyme. |
Related PDB | 1c60 1c61 1c62 1c63 1c64 1c65 1c66 1c67 1c68 1c69 1c6a 1c6b 1c6c 1c6d 1c6e 1c6f 1c6g 1c6h 1c6i 1c6j 1c6k 1c6l 1c6m 1c6n 1c6p 1c6q 1c6t |
Related UniProtKB | |
[81] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10618384 |
Journal | Proc Natl Acad Sci U S A |
Year | 2000 |
Volume | 97 |
Pages | 139-44 |
Authors | Yang G, Cecconi C, Baase WA, Vetter IR, Breyer WA, Haack JA, Matthews BW, Dahlquist FW, Bustamante C |
Title | Solid-state synthesis and mechanical unfolding of polymers of T4 lysozyme. |
Related PDB | 1b6i |
Related UniProtKB | |
[82] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10835104 |
Journal | Protein Eng |
Year | 2000 |
Volume | 13 |
Pages | 313-21 |
Authors | Wray JW, Baase WA, Ostheimer GJ, Zhang XJ, Matthews BW |
Title | Use of a non-rigid region in T4 lysozyme to design an adaptable metal-binding site. |
Related PDB | 1epy 257l 258l 260l |
Related UniProtKB | |
[83] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11300763 |
Journal | Biochemistry |
Year | 2001 |
Volume | 40 |
Pages | 3828-46 |
Authors | Columbus L, Kalai T, Jeko J, Hideg K, Hubbell WL |
Title | Molecular motion of spin labeled side chains in alpha-helices: analysis by variation of side chain structure. |
Related PDB | |
Related UniProtKB | |
[84] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11341831 |
Journal | Biochemistry |
Year | 2001 |
Volume | 40 |
Pages | 5665-73 |
Authors | Leung AK, Duewel HS, Honek JF, Berghuis AM |
Title | Crystal structure of the lytic transglycosylase from bacteriophage lambda in complex with hexa-N-acetylchitohexaose. |
Related PDB | |
Related UniProtKB | |
[85] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11350172 |
Journal | J Mol Biol |
Year | 2001 |
Volume | 308 |
Pages | 745-64 |
Authors | Goto NK, Skrynnikov NR, Dahlquist FW, Kay LE |
Title | What is the average conformation of bacteriophage T4 lysozyme in solution? A domain orientation study using dipolar couplings measured by solution NMR. |
Related PDB | |
Related UniProtKB | |
[86] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11316887 |
Journal | Protein Sci |
Year | 2001 |
Volume | 10 |
Pages | 1067-78 |
Authors | Xu J, Baase WA, Quillin ML, Baldwin EP, Matthews BW |
Title | Structural and thermodynamic analysis of the binding of solvent at internal sites in T4 lysozyme. |
Related PDB | 1g06 1g07 1g0g 1g0j 1g0k 1g0l 1g0m 1g0p 1g0q 1g1v 1g1w 1i6s |
Related UniProtKB | |
[87] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 12487988 |
Journal | Biophys Chem |
Year | 2002 |
Volume | 101-102 |
Pages | 43-56 |
Authors | Zhang X, Baase WA, Matthews BW |
Title | A helix initiation signal in T4 lysozyme identified by polyalanine mutagenesis. |
Related PDB | 190l 191l 192l 1d9w |
Related UniProtKB | |
[88] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11996571 |
Journal | J Am Chem Soc |
Year | 2002 |
Volume | 124 |
Pages | 5304-14 |
Authors | Borbat PP, McHaourab HS, Freed JH |
Title | Protein structure determination using long-distance constraints from double-quantum coherence ESR: study of T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[89] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11841314 |
Journal | J Am Chem Soc |
Year | 2002 |
Volume | 124 |
Pages | 1443-51 |
Authors | Mulder FA, Hon B, Mittermaier A, Dahlquist FW, Kay LE |
Title | Slow internal dynamics in proteins: application of NMR relaxation dispersion spectroscopy to methyl groups in a cavity mutant of T4 lysozyme. |
Related PDB | |
Related UniProtKB | |
[90] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11884133 |
Journal | J Mol Biol |
Year | 2002 |
Volume | 316 |
Pages | 931-40 |
Authors | Sagermann M, Matthews BW |
Title | Crystal structures of a T4-lysozyme duplication-extension mutant demonstrate that the highly conserved beta-sheet region has low intrinsic folding propensity. |
Related PDB | 1jtm |
Related UniProtKB | |
[91] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 12217695 |
Journal | J Mol Biol |
Year | 2002 |
Volume | 322 |
Pages | 339-55 |
Authors | Wei BQ, Baase WA, Weaver LH, Matthews BW, Shoichet BK |
Title | A model binding site for testing scoring functions in molecular docking. |
Related PDB | 1lgu 1lgw 1lgx 1li2 1li3 1li6 |
Related UniProtKB | |
[92] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12364581 |
Journal | Protein Eng |
Year | 2002 |
Volume | 15 |
Pages | 669-75 |
Authors | Machicado C, Bueno M, Sancho J |
Title | Predicting the structure of protein cavities created by mutation. |
Related PDB | |
Related UniProtKB | |
[93] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11847274 |
Journal | Protein Sci |
Year | 2002 |
Volume | 11 |
Pages | 516-21 |
Authors | Sagermann M, Martensson LG, Baase WA, Matthews BW |
Title | A test of proposed rules for helix capping: implications for protein design. |
Related PDB | 1jqu 1llh |
Related UniProtKB | |
[94] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 12646375 |
Journal | Biophys Chem |
Year | 2003 |
Volume | 100 |
Pages | 325-40 |
Authors | Gassner NC, Baase WA, Mooers BH, Busam RD, Weaver LH, Lindstrom JD, Quillin ML, Matthews BW |
Title | Multiple methionine substitutions are tolerated in T4 lysozyme and have coupled effects on folding and stability. |
Related PDB | 1ks3 1kw5 1kw7 1ky0 1ky1 1l0j 1l0k 1lpy 1lw9 1lwg 1lwk |
Related UniProtKB | |
[95] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12770868 |
Journal | Biophys J |
Year | 2003 |
Volume | 84 |
Pages | 3583-93 |
Authors | Zhang Z, Shi Y, Liu H |
Title | Molecular dynamics simulations of peptides and proteins with amplified collective motions. |
Related PDB | |
Related UniProtKB | |
[96] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 12963380 |
Journal | J Mol Biol |
Year | 2003 |
Volume | 332 |
Pages | 741-56 |
Authors | Mooers BH, Datta D, Baase WA, Zollars ES, Mayo SL, Matthews BW |
Title | Repacking the Core of T4 lysozyme by automated design. |
Related PDB | 1p2l 1p2r 1p36 1p37 1p3n 1p46 1p64 1p6y 1p7s 1pqd 1pqi 1pqj 1pqk 1pqm 1pqo |
Related UniProtKB | |
[97] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 12869697 |
Journal | Proc Natl Acad Sci U S A |
Year | 2003 |
Volume | 100 |
Pages | 9191-5 |
Authors | Sagermann M, Gay L, Matthews BW |
Title | Long-distance conformational changes in a protein engineered by modulated sequence duplication |
Related PDB | 1oyu |
Related UniProtKB | |
[98] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 14756565 |
Journal | Biochemistry |
Year | 2004 |
Volume | 43 |
Pages | 1296-301 |
Authors | Sagermann M, Baase WA, Mooers BH, Gay L, Matthews BW |
Title | Relocation or duplication of the helix A sequence of T4 lysozyme causes only modest changes in structure but can increase or decrease the rate of folding. |
Related PDB | |
Related UniProtKB |
Comments |
---|
This enzyme belongs to the glycosidase family-24, According to the literature [61], (1) Asp20 acts as a general base to acitivate a nearby water molecule. (2) The activated water makes a nucleophilic attack on the C1-atom of glycosidic bond, However, In contrast to the wild-type enzyme, |
Created | Updated |
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2004-09-27 | 2009-02-26 |