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2VJO

Formyl-CoA transferase mutant variant Q17A with aspartyl-CoA thioester intermediates and oxalate

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005737cellular_componentcytoplasm
A0008410molecular_functionCoA-transferase activity
A0016740molecular_functiontransferase activity
A0033608molecular_functionformyl-CoA transferase activity
A0033611biological_processoxalate catabolic process
B0003824molecular_functioncatalytic activity
B0005737cellular_componentcytoplasm
B0008410molecular_functionCoA-transferase activity
B0016740molecular_functiontransferase activity
B0033608molecular_functionformyl-CoA transferase activity
B0033611biological_processoxalate catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues23
DetailsBINDING SITE FOR RESIDUE COA A1169
ChainResidue
AHIS15
APHE97
AGLY98
AARG104
AMET105
AVAL124
ALYS137
AVAL138
ATYR139
AASP169
AMET200
AALA18
AHOH2078
AHOH2079
AHOH2080
AHOH2081
AARG38
AMET44
ALEU72
AASP73
AMET74
ALYS75
AASN96

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL A1429
ChainResidue
AALA17
APHE63
AALA166
ASER170

site_idAC3
Number of Residues20
DetailsBINDING SITE FOR RESIDUE COA B1169
ChainResidue
ALYS52
BHIS15
BALA17
BALA18
BARG38
BLEU72
BASP73
BMET74
BLYS75
BASN96
BPHE97
BGLY98
BARG104
BMET105
BLYS137
BVAL138
BASP169
BHOH2049
BHOH2087
BHOH2088

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL B1429
ChainResidue
BPHE63
BALA166
BASP169
BSER170
BHOH2073

site_idAC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE OXL A1430
ChainResidue
AGLY258
AGLY260
AGLY261
AGLN262
AHOH2245
AHOH2246
BGLU140
BHOH2037

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE EPE A1431
ChainResidue
ATRP272
ATHR274
AASP275
AALA276
AHOH2144
AHOH2147
AHOH2148
AHOH2248
AHOH2249
BASP157
BGLY158

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000255|HAMAP-Rule:MF_00742, ECO:0000269|PubMed:15213226
ChainResidueDetails
AASP169
BASP169

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING:
ChainResidueDetails
AHIS15
BGLY260
ALEU72
AASN96
ALYS137
AGLY260
BHIS15
BLEU72
BASN96
BLYS137

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00742, ECO:0000269|PubMed:12839984, ECO:0000269|PubMed:15213226, ECO:0000269|PubMed:18162462
ChainResidueDetails
AARG38
AARG104
BARG38
BARG104

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
AASP169

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
BASP169

site_idMCSA1
Number of Residues5
DetailsM-CSA 155
ChainResidueDetails
AALA17electrostatic stabiliser, hydrogen bond donor
AGLU140electrostatic stabiliser, hydrogen bond donor
AASP169covalently attached, electrofuge, electrophile, nucleofuge, nucleophile
AGLY260electrostatic stabiliser, hydrogen bond acceptor
AGLY261electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues5
DetailsM-CSA 155
ChainResidueDetails
BALA17electrostatic stabiliser, hydrogen bond donor
BGLU140electrostatic stabiliser, hydrogen bond donor
BASP169covalently attached, electrofuge, electrophile, nucleofuge, nucleophile
BGLY260electrostatic stabiliser, hydrogen bond acceptor
BGLY261electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-07-17

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