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6OI9

Crystal Structure of E. coli Biotin Carboxylase Complexed with 7-[3-(aminomethyl)pyrrolidin-1-yl]-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-2-amine

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0003989molecular_functionacetyl-CoA carboxylase activity
A0004075molecular_functionbiotin carboxylase activity
A0005515molecular_functionprotein binding
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006633biological_processfatty acid biosynthetic process
A0009317cellular_componentacetyl-CoA carboxylase complex
A0016874molecular_functionligase activity
A0042803molecular_functionprotein homodimerization activity
A0045717biological_processnegative regulation of fatty acid biosynthetic process
A0046872molecular_functionmetal ion binding
A2001295biological_processmalonyl-CoA biosynthetic process
B0003824molecular_functioncatalytic activity
B0003989molecular_functionacetyl-CoA carboxylase activity
B0004075molecular_functionbiotin carboxylase activity
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006633biological_processfatty acid biosynthetic process
B0009317cellular_componentacetyl-CoA carboxylase complex
B0016874molecular_functionligase activity
B0042803molecular_functionprotein homodimerization activity
B0045717biological_processnegative regulation of fatty acid biosynthetic process
B0046872molecular_functionmetal ion binding
B2001295biological_processmalonyl-CoA biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues14
Detailsbinding site for residue MQM A 501
ChainResidue
AILE157
AHIS236
AGLU276
ALEU278
AGLU288
AILE437
ALYS159
AGLY166
AGLU201
ALYS202
ATYR203
ALEU204
AHIS209
AGLN233

site_idAC2
Number of Residues4
Detailsbinding site for residue EDO A 502
ChainResidue
AHIS236
AGLN237
ALYS238
AARG338

site_idAC3
Number of Residues8
Detailsbinding site for residue EDO A 503
ChainResidue
AILE120
AGLY133
ASER134
AASP135
AGLY136
ATYR199
AHOH660
AHOH708

site_idAC4
Number of Residues14
Detailsbinding site for residue MQM B 501
ChainResidue
BILE157
BLYS159
BGLY166
BGLU201
BLYS202
BTYR203
BLEU204
BHIS209
BGLN233
BHIS236
BGLU276
BLEU278
BGLU288
BILE437

site_idAC5
Number of Residues7
Detailsbinding site for residue EDO B 502
ChainResidue
AVAL365
AARG366
ATRP367
BPRO360
BGLY361
BGLY362
BVAL365

Functional Information from PROSITE/UniProt
site_idPS00866
Number of Residues15
DetailsCPSASE_1 Carbamoyl-phosphate synthase subdomain signature 1. YPVIIKASgggGGrG
ChainResidueDetails
ATYR154-GLY168

site_idPS00867
Number of Residues8
DetailsCPSASE_2 Carbamoyl-phosphate synthase subdomain signature 2. FIEMNTRI
ChainResidueDetails
APHE286-ILE293

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: ACT_SITE => ECO:0000269|PubMed:19213731
ChainResidueDetails
AARG292
BARG292

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8D
ChainResidueDetails
ALYS116
AGLY165
BLYS116
BGLY165

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:19213731, ECO:0007744|PDB:3G8C, ECO:0007744|PDB:3G8D
ChainResidueDetails
ALYS159
BLYS159

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8C, ECO:0007744|PDB:3G8D
ChainResidueDetails
AGLU201
BGLU201

site_idSWS_FT_FI5
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:19213731, ECO:0007744|PDB:3G8C
ChainResidueDetails
AHIS209
BARG338
ALYS238
AARG292
AVAL295
AARG338
BHIS209
BLYS238
BARG292
BVAL295

site_idSWS_FT_FI6
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8C
ChainResidueDetails
AHIS236
BHIS236

site_idSWS_FT_FI7
Number of Residues6
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00409
ChainResidueDetails
AGLU276
AGLU288
AASN290
BGLU276
BGLU288
BASN290

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PDB entries from 2024-07-17

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