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1WDK

fatty acid beta-oxidation multienzyme complex from Pseudomonas fragi, form I (native2)

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0003857molecular_function3-hydroxyacyl-CoA dehydrogenase activity
A0004165molecular_functiondelta(3)-delta(2)-enoyl-CoA isomerase activity
A0004300molecular_functionenoyl-CoA hydratase activity
A0005515molecular_functionprotein binding
A0006631biological_processfatty acid metabolic process
A0006635biological_processfatty acid beta-oxidation
A0008692molecular_function3-hydroxybutyryl-CoA epimerase activity
A0009056biological_processcatabolic process
A0009062biological_processfatty acid catabolic process
A0016042biological_processlipid catabolic process
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0016829molecular_functionlyase activity
A0016853molecular_functionisomerase activity
A0036125cellular_componentfatty acid beta-oxidation multienzyme complex
A0070403molecular_functionNAD+ binding
B0003824molecular_functioncatalytic activity
B0003857molecular_function3-hydroxyacyl-CoA dehydrogenase activity
B0004165molecular_functiondelta(3)-delta(2)-enoyl-CoA isomerase activity
B0004300molecular_functionenoyl-CoA hydratase activity
B0005515molecular_functionprotein binding
B0006631biological_processfatty acid metabolic process
B0006635biological_processfatty acid beta-oxidation
B0008692molecular_function3-hydroxybutyryl-CoA epimerase activity
B0009056biological_processcatabolic process
B0009062biological_processfatty acid catabolic process
B0016042biological_processlipid catabolic process
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0016829molecular_functionlyase activity
B0016853molecular_functionisomerase activity
B0036125cellular_componentfatty acid beta-oxidation multienzyme complex
B0070403molecular_functionNAD+ binding
C0003988molecular_functionacetyl-CoA C-acyltransferase activity
C0005515molecular_functionprotein binding
C0005737cellular_componentcytoplasm
C0006631biological_processfatty acid metabolic process
C0006635biological_processfatty acid beta-oxidation
C0010124biological_processphenylacetate catabolic process
C0016042biological_processlipid catabolic process
C0016746molecular_functionacyltransferase activity
C0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
D0003988molecular_functionacetyl-CoA C-acyltransferase activity
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0006631biological_processfatty acid metabolic process
D0006635biological_processfatty acid beta-oxidation
D0010124biological_processphenylacetate catabolic process
D0016042biological_processlipid catabolic process
D0016746molecular_functionacyltransferase activity
D0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE HG D 1
ChainResidue
DCYS95
DMET151
DPHE349
DACO4001

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE HG C 392
ChainResidue
CCYS95
CMET151
CPHE349
CACO3001

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 716
ChainResidue
AASP573
DGLU266
DVAL391
AHIS550

site_idAC4
Number of Residues19
DetailsBINDING SITE FOR RESIDUE ACO C 3001
ChainResidue
CCYS95
CMET130
CMET151
CHIS177
CARG215
CTHR218
CLEU223
CPHE230
CALA239
CGLY240
CSER243
CILE245
CMET284
CALA314
CPHE315
CHIS347
CCYS377
CHG392
CHOH3206

site_idAC5
Number of Residues22
DetailsBINDING SITE FOR RESIDUE ACO D 4001
ChainResidue
DHG1
DCYS95
DMET130
DMET151
DHIS177
DARG215
DTHR218
DLEU223
DALA239
DGLY240
DSER243
DMET284
DASN312
DALA314
DPHE315
DHIS347
DCYS377
DGLY379
DHOH4152
DHOH4155
DHOH4169
DHOH4174

site_idAC6
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NAD A 1001
ChainResidue
AGLY321
AALA322
AILE324
AMET325
AASP344
AILE345
AASN346
AGLY349
AVAL401
AGLU403
ALYS408
AVAL411
AASN428
ATHR429
ASER430
APHE452
AASN454
AHOH1087
AHOH1177

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE N8E A 1002
ChainResidue
AMET459
AASN501
AVAL659
ATYR660
AGLY661
AILE662

site_idAC8
Number of Residues12
DetailsBINDING SITE FOR RESIDUE N8E A 1003
ChainResidue
AGLY68
AALA69
AASP70
AILE71
APHE74
AGLY116
AGLY117
APRO139
AGLU140
ALEU143
AGLN298
ALYS305

site_idAC9
Number of Residues17
DetailsBINDING SITE FOR RESIDUE NAD B 2001
ChainResidue
BVAL411
BASN428
BTHR429
BSER430
BASN454
BHOH2046
BHOH2288
BHOH2312
BGLY321
BALA322
BILE324
BMET325
BASP344
BILE345
BVAL401
BGLU403
BLYS408

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE N8E B 2002
ChainResidue
BMET459
BPRO460
BASN501
BMET535
BVAL659
BTYR660
BGLY661
BGLY663

site_idBC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE N8E B 2003
ChainResidue
BARG34
BLEU37
BGLU73
BASN77
BLEU80
BGLY88
BGLU120
BGLU140
BGLY148
BPHE149
BHOH2309

Functional Information from PROSITE/UniProt
site_idPS00067
Number of Residues25
Details3HCDH 3-hydroxyacyl-CoA dehydrogenase signature. DcpGFLvNRvlfPYFggfak.LVsaG
ChainResidueDetails
AASP494-GLY518

site_idPS00098
Number of Residues19
DetailsTHIOLASE_1 Thiolases acyl-enzyme intermediate signature. VSRlCGSSMsALhtaaqaI
ChainResidueDetails
CVAL91-ILE109

site_idPS00099
Number of Residues14
DetailsTHIOLASE_3 Thiolases active site. GLSTMCIGlGqGiA
ChainResidueDetails
CGLY372-ALA385

site_idPS00166
Number of Residues21
DetailsENOYL_COA_HYDRATASE Enoyl-CoA hydratase/isomerase signature. VAaINGialGGGlemcLaADF
ChainResidueDetails
AVAL107-PHE127

site_idPS00178
Number of Residues11
DetailsAA_TRNA_LIGASE_I Aminoacyl-transfer RNA synthetases class-I signature. Pk.GGtVTAGTS
ChainResidueDetails
CPRO232-SER242

site_idPS00737
Number of Residues17
DetailsTHIOLASE_2 Thiolases signature 2. NlhGGaIAlGHPfGcSG
ChainResidueDetails
CASN337-GLY353

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Acyl-thioester intermediate => ECO:0000255|HAMAP-Rule:MF_01620
ChainResidueDetails
CGLY96
DGLY96

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_01620
ChainResidueDetails
CPRO348
BASP297
BMET325
BASP344
BVAL401
BLYS408
BSER430
BASN454
BASN501
BTYR660
CILE378
DPRO348
DILE378
ALYS408
ASER430
AASN454
AASN501
ATYR660

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: Important for catalytic activity => ECO:0000255|HAMAP-Rule:MF_01621
ChainResidueDetails
AGLU120
AGLU140
BGLU120
BGLU140

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
CHIS347
CCYS377
CCYS95
CGLY379

site_idCSA10
Number of Residues2
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
BGLU140
BGLY148

site_idCSA11
Number of Residues3
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AGLU120
AGLU140
AGLY117

site_idCSA12
Number of Residues3
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
BGLU120
BGLU140
BGLY117

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
DHIS347
DCYS377
DCYS95
DGLY379

site_idCSA3
Number of Residues4
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AGLU120
AGLU140
AGLY117
AALA69

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
BGLU120
BGLU140
BGLY117
BALA69

site_idCSA5
Number of Residues2
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
CHIS347
CCYS377

site_idCSA6
Number of Residues2
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
DHIS347
DCYS377

site_idCSA7
Number of Residues3
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AHIS451
ASER430
AASN501

site_idCSA8
Number of Residues3
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
BHIS451
BSER430
BASN501

site_idCSA9
Number of Residues2
DetailsAnnotated By Reference To The Literature 1afw
ChainResidueDetails
AGLU140
AGLY148

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PDB entries from 2024-10-30

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