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. Involvement of N-acetamido groups.
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, glycine 156----aspartic acid.
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. The temperature-sensitive mutant protein Thr157----Ile.
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, Arg 96----His.
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, medium, and high ionic strengths.
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, Ile3-->Pro.
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, additive effects on both structure and stability.
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, stability, solvation, and spectroscopic properties.
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. Sites 44 and 131 in bacteriophage T4 lysozyme.
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. Structural and thermodynamic analysis.
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. Hinge-bending motion and the substrate-induced conformational transition studied by site-directed spin labeling.
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
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[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
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[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
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[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.
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Comments
This enzyme belongs to the glycosidase family-24, which seems to have an inverting mechanism. It converts the configuration of substrate saccharide from equatorial one (or beta-anomer) to axial conformation (or alpha-anomer) (see [77]).
According to the literature [61], [64] & [77], the catalytic reaction proceeds in a single displacement mechanism, as follows:
(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, releasing an alpha-anomer, whilst Glu11 acts as a general acid to protonate the oxygen atom of the glycosidic bond, resulting in the formation of alpha-anomer product.
However, the paper [77] suggested that Asp20 is not so essential as Glu11. A counterpart of this residue in Goose lysozyme does not exist (see [59]).
In contrast to the wild-type enzyme, the mutant T26H has got a double displacement mechanism, in which the mutated residue, His26, acts as a nucleophile to form a covalent-bonded intermediate, releasing beta-anomer products (see [61], [64] & [77]).

Created Updated
2004-09-27 2009-02-26