DB code: D00090
CATH domain | 3.40.47.10 : Peroxisomal Thiolase; Chain A, domain 1 | Catalytic domain |
---|---|---|
3.40.47.20 : Peroxisomal Thiolase; Chain A, domain 1 | Catalytic domain | |
E.C. | 2.3.1.16 | |
CSA | 1afw | |
M-CSA | 1afw | |
MACiE | M0077 |
CATH domain | Related DB codes (homologues) |
---|---|
3.40.47.10 : Peroxisomal Thiolase; Chain A, domain 1 | D00411 D00509 D00825 D00826 D00867 D00871 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | Pfam |
---|---|---|---|---|
P27796 |
3-ketoacyl-CoA thiolase, peroxisomal
|
EC
2.3.1.16
Beta-ketothiolase Acetyl-CoA acyltransferase Peroxisomal 3-oxoacyl-CoA thiolase |
NP_012106.1
(Protein)
NM_001179508.1 (DNA/RNA sequence) |
PF02803
(Thiolase_C)
PF00108 (Thiolase_N) [Graphical View] |
KEGG enzyme name |
---|
acetyl-CoA C-acyltransferase
beta-ketothiolase 3-ketoacyl-CoA thiolase KAT beta-ketoacyl coenzyme A thiolase beta-ketoacyl-CoA thiolase beta-ketoadipyl coenzyme A thiolase beta-ketoadipyl-CoA thiolase 3-ketoacyl CoA thiolase 3-ketoacyl coenzyme A thiolase 3-ketoacyl thiolase 3-ketothiolase 3-oxoacyl-CoA thiolase 3-oxoacyl-coenzyme A thiolase 6-oxoacyl-CoA thiolase acetoacetyl-CoA beta-ketothiolase acetyl-CoA acyltransferase ketoacyl-CoA acyltransferase ketoacyl-coenzyme A thiolase long-chain 3-oxoacyl-CoA thiolase oxoacyl-coenzyme A thiolase pro-3-ketoacyl-CoA thiolase thiolase I 2-methylacetoacetyl-CoA thiolase [misleading] |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P27796 | THIK_YEAST | Acyl-CoA + acetyl-CoA = CoA + 3-oxoacyl-CoA. | Homodimer. | Peroxisome. |
KEGG Pathways | Map code | Pathways | E.C. |
---|---|---|
MAP00062 | Fatty acid elongation in mitochondria | |
MAP00071 | Fatty acid metabolism | |
MAP00120 | Bile acid biosynthesis | |
MAP00280 | Valine, leucine and isoleucine degradation | |
MAP00281 | Geraniol degradation | |
MAP00362 | Benzoate degradation via hydroxylation | |
MAP00592 | alpha-Linolenic acid metabolism | |
MAP00642 | Ethylbenzene degradation | |
MAP01040 | Biosynthesis of unsaturated fatty acids |
Compound table | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Substrates | Products | Intermediates | ||||||||
KEGG-id | C00040 | C00024 | C00010 | C00264 | ||||||
E.C. | ||||||||||
Compound | Acyl-CoA | Acetyl-CoA | CoA | 3-Oxoacyl-CoA | ||||||
Type | amine group,carbohydrate,nucleotide ,peptide/protein,sulfide group | amine group,carbohydrate,nucleotide ,peptide/protein,sulfide group | amine group,carbohydrate,nucleotide ,peptide/protein,sulfhydryl group | amine group,carbohydrate,nucleotide ,peptide/protein,phosphate group/phosphate ion,sulfide group | ||||||
ChEBI |
15351 15351 |
15346 15346 |
||||||||
PubChem |
444493 6302 444493 6302 |
6816 87642 6816 87642 |
||||||||
1afwA01 | Unbound | Unbound | Unbound | Unbound | ||||||
1afwB01 | Unbound | Unbound | Unbound | Unbound | ||||||
1pxtA01 | Unbound | Unbound | Unbound | Unbound | ||||||
1pxtB01 | Unbound | Unbound | Unbound | Unbound | ||||||
1afwA02 | Unbound | Unbound | Unbound | Unbound | ||||||
1afwB02 | Unbound | Unbound | Unbound | Unbound | ||||||
1pxtA02 | Unbound | Unbound | Unbound | Unbound | ||||||
1pxtB02 | Unbound | Unbound | Unbound | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
PDB;1Swiss-prot;P27796 |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
1afwA01 | CYS 125 | |||||||||
1afwB01 | CYS 125 | |||||||||
1pxtA01 | CYS 125 | |||||||||
1pxtB01 | CYS 125 | |||||||||
1afwA02 | HIS 375;CYS 403 | |||||||||
1afwB02 | HIS 375;CYS 403 | |||||||||
1pxtA02 | HIS 375;CYS 403 | |||||||||
1pxtB02 | HIS 375;CYS 403 |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[3]
|
p.800-801, p.804, Fig.13 | |
[5]
|
p.723, Fig.9 | 4 |
References | |
---|---|
[1] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 2859988 |
Journal | Eur J Biochem |
Year | 1985 |
Volume | 149 |
Pages | 181-6 |
Authors | Mori M, Matsue H, Miura S, Tatibana M, Hashimoto T |
Title |
Transport of proteins into mitochondrial matrix. |
Related PDB | |
Related UniProtKB | |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 2213879 |
Journal | J Mol Biol |
Year | 1990 |
Volume | 215 |
Pages | 211-3 |
Authors | Zeelen JP, Wierenga RK, Erdmann R, Kunau WH |
Title | Crystallographic studies of 3-ketoacylCoA thiolase from yeast Saccharomyces cerevisiae. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.8 ANGSTROMS) |
Medline ID | 95111951 |
PubMed ID | 7812714 |
Journal | Structure |
Year | 1994 |
Volume | 2 |
Pages | 797-808 |
Authors | Mathieu M, Zeelen JP, Pauptit RA, Erdmann R, Kunau WH, Wierenga RK |
Title | The 2.8 A crystal structure of peroxisomal 3-ketoacyl-CoA thiolase of Saccharomyces cerevisiae: a five-layered alpha beta alpha beta alpha structure constructed from two core domains of identical topology. |
Related PDB | 1pxt |
Related UniProtKB | P27796 |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7756275 |
Journal | Biochemistry |
Year | 1995 |
Volume | 34 |
Pages | 6441-7 |
Authors | Yang SY, He XY, Schulz H |
Title |
Glutamate 139 of the large alpha-subunit is the catalytic base in the dehydration of both D- and L-3-hydroxyacyl-coenzyme A but not in the isomerization of delta 3, |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.8 ANGSTROMS) |
Medline ID | 98022915 |
PubMed ID | 9402066 |
Journal | J Mol Biol |
Year | 1997 |
Volume | 273 |
Pages | 714-28 |
Authors | Mathieu M, Modis Y, Zeelen JP, Engel CK, Abagyan RA, Ahlberg A, Rasmussen B, Lamzin VS, Kunau WH, Wierenga RK |
Title | The 1.8 A crystal structure of the dimeric peroxisomal 3-ketoacyl-CoA thiolase of Saccharomyces cerevisiae: implications for substrate binding and reaction mechanism. |
Related PDB | 1afw 1afy |
Related UniProtKB | P27796 |
[6] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9215574 |
Journal | Protein Eng |
Year | 1997 |
Volume | 10 |
Pages | 561-6 |
Authors | Rangan VS, Serre L, Witkowska HE, Bari A, Smith S |
Title | Characterization of the malonyl-/acetyltransacylase domain of the multifunctional animal fatty acid synthase by expression in Escherichia coli and refolding in vitro. |
Related PDB | |
Related UniProtKB | |
[7] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9744475 |
Journal | Hum Mutat |
Year | 1998 |
Volume | 12 |
Pages | 245-54 |
Authors | Fukao T, Nakamura H, Song XQ, Nakamura K, Orii KE, Kohno Y, Kano M, Yamaguchi S, Hashimoto T, Orii T, Kondo N |
Title |
Characterization of N93S, |
Related PDB | |
Related UniProtKB | |
[8] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10098837 |
Journal | J Neurochem |
Year | 1999 |
Volume | 72 |
Pages | 1362-71 |
Authors | Ballestero RP, Dybowski JA, Levy G, Agranoff BW, Uhler MD |
Title |
Cloning and characterization of zRICH, |
Related PDB | |
Related UniProtKB | |
[9] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10727229 |
Journal | Biochemistry |
Year | 2000 |
Volume | 39 |
Pages | 3360-8 |
Authors | Vinarov DA, Miziorko HM |
Title | 3-hydroxy-3-methylglutaryl-coenzyme A synthase reaction intermediates: detection of a covalent tetrahedral adduct by differential isotope shift 13C nuclear magnetic resonance spectroscopy. |
Related PDB | |
Related UniProtKB | |
[10] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11915938 |
Journal | Cell Mol Life Sci |
Year | 2002 |
Volume | 59 |
Pages | 193-212 |
Authors | Stolowich NJ, Petrescu AD, Huang H, Martin GG, Scott AI, Schroeder F |
Title | Sterol carrier protein-2: structure reveals function. |
Related PDB | |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11914035 |
Journal | Mol Genet Metab |
Year | 2002 |
Volume | 75 |
Pages | 235-43 |
Authors | Fukao T, Nakamura H, Nakamura K, Perez-Cerda C, Baldellou A, Barrionuevo CR, Castello FG, Kohno Y, Ugarte M, Kondo N |
Title | Characterization of six mutations in five Spanish patients with mitochondrial acetoacetyl-CoA thiolase deficiency: effects of amino acid substitutions on tertiary structure. |
Related PDB | |
Related UniProtKB |
Comments |
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Created | Updated |
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2004-03-17 | 2009-02-26 |