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1WL4

Human cytosolic acetoacetyl-CoA thiolase complexed with CoA

Functional Information from GO Data
ChainGOidnamespacecontents
A0003985molecular_functionacetyl-CoA C-acetyltransferase activity
A0005515molecular_functionprotein binding
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006629biological_processlipid metabolic process
A0006631biological_processfatty acid metabolic process
A0006635biological_processfatty acid beta-oxidation
A0016746molecular_functionacyltransferase activity
A0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
A0070062cellular_componentextracellular exosome
Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SO4 A 3001
ChainResidue
ASER12
AHOH3118
AALA13
AARG44
ALEU277
AASN338
AHIS368
AHOH3022
AHOH3060
AHOH3090

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 A 3002
ChainResidue
ATYR81
AHIS156
AGLU289
APRO290
ASER291
AHOH3207
AHOH3279
AHOH3483
AHOH3502

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 3003
ChainResidue
AGLU215
AVAL216
ALYS217
ATHR218
AHOH3408
AHOH3440
AHOH3498

site_idAC4
Number of Residues28
DetailsBINDING SITE FOR RESIDUE COA A 1001
ChainResidue
ALYS136
ALEU151
AHIS159
AGLN186
AARG223
ASER226
AMET231
ATYR237
APRO248
AALA249
ASER252
AGLY253
AMET293
APHE324
AGOL2001
AHOH3024
AHOH3041
AHOH3050
AHOH3053
AHOH3062
AHOH3068
AHOH3087
AHOH3164
AHOH3225
AHOH3273
AHOH3278
AHOH3351
AHOH3368

site_idAC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 2001
ChainResidue
AARG223
AHIS224
AGLY225
AASN227
AALA230
ACOA1001
AHOH3041
AHOH3465

site_idAC6
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 2002
ChainResidue
AASN187
AGLU190
AASN191
AASP270
ALYS271
AHOH3402
AHOH3495
AHOH3507
AHOH3546

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 2003
ChainResidue
AVAL75
AGLY78
AILE79
APRO80
ALYS170

Functional Information from PROSITE/UniProt
site_idPS00099
Number of Residues14
DetailsTHIOLASE_3 Thiolases active site. GVAALCIGgGmGiA
ChainResidueDetails
AGLY378-ALA391

site_idPS00737
Number of Residues17
DetailsTHIOLASE_2 Thiolases signature 2. NieGGaIAlGHPlGaSG
ChainResidueDetails
AASN343-GLY359

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Acyl-thioester intermediate => ECO:0000305|PubMed:15733928
ChainResidueDetails
ACSO92

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor/acceptor => ECO:0000305|PubMed:15733928
ChainResidueDetails
ACYS383

site_idSWS_FT_FI3
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:15733928, ECO:0007744|PDB:1WL4
ChainResidueDetails
AARG223
ASER226
ASER252

site_idSWS_FT_FI4
Number of Residues1
DetailsSITE: Increases nucleophilicity of active site Cys => ECO:0000250|UniProtKB:P42765
ChainResidueDetails
AHIS353

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: N-acetylmethionine => ECO:0007744|PubMed:19413330, ECO:0007744|PubMed:22223895, ECO:0007744|PubMed:22814378
ChainResidueDetails
AMET1

site_idSWS_FT_FI6
Number of Residues3
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS200
ALYS233
ALYS235

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AHIS353
ACYS383
AGLY385

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AHIS353
ACYS383

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PDB entries from 2024-05-01

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