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1BQ4

SACCHAROMYCES CEREVISIAE PHOSPHOGLYCERATE MUTASE IN COMPLEX WITH BENZENE HEXACARBOXYLATE

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004619molecular_functionphosphoglycerate mutase activity
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005741cellular_componentmitochondrial outer membrane
A0005758cellular_componentmitochondrial intermembrane space
A0005829cellular_componentcytosol
A0006094biological_processgluconeogenesis
A0006096biological_processglycolytic process
A0016853molecular_functionisomerase activity
A0016868molecular_functionintramolecular phosphotransferase activity
A0046538molecular_function2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity
B0003824molecular_functioncatalytic activity
B0004619molecular_functionphosphoglycerate mutase activity
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005741cellular_componentmitochondrial outer membrane
B0005758cellular_componentmitochondrial intermembrane space
B0005829cellular_componentcytosol
B0006094biological_processgluconeogenesis
B0006096biological_processglycolytic process
B0016853molecular_functionisomerase activity
B0016868molecular_functionintramolecular phosphotransferase activity
B0046538molecular_function2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity
C0003824molecular_functioncatalytic activity
C0004619molecular_functionphosphoglycerate mutase activity
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005741cellular_componentmitochondrial outer membrane
C0005758cellular_componentmitochondrial intermembrane space
C0005829cellular_componentcytosol
C0006094biological_processgluconeogenesis
C0006096biological_processglycolytic process
C0016853molecular_functionisomerase activity
C0016868molecular_functionintramolecular phosphotransferase activity
C0046538molecular_function2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity
D0003824molecular_functioncatalytic activity
D0004619molecular_functionphosphoglycerate mutase activity
D0005737cellular_componentcytoplasm
D0005739cellular_componentmitochondrion
D0005741cellular_componentmitochondrial outer membrane
D0005758cellular_componentmitochondrial intermembrane space
D0005829cellular_componentcytosol
D0006094biological_processgluconeogenesis
D0006096biological_processglycolytic process
D0016853molecular_functionisomerase activity
D0016868molecular_functionintramolecular phosphotransferase activity
D0046538molecular_function2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 D 300
ChainResidue
DHIS8
DSER11
DASN14
DTHR20
DARG59

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 C 301
ChainResidue
CSER11
CASN14
CTHR20
CARG59

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 303
ChainResidue
BHIS8
BSER11
BASN14
BTHR20
BARG59

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE BHC A 302
ChainResidue
AARG7
AASN14
ATYR89
ALYS97
AARG113
AARG114
AASN183
AASN204

site_idCAA
Number of Residues4
DetailsCATALYTIC SITE. HIS 8 PHOSPHORYLATION IS REQUIRED TO PRIME THE ENZYME.
ChainResidue
AHIS8
AHIS181
AARG7
AGLU86

site_idCAB
Number of Residues4
DetailsCATALYTIC SITE. HIS 8 PHOSPHORYLATION IS REQUIRED TO PRIME THE ENZYME.
ChainResidue
BHIS8
BHIS181
BARG7
BGLU86

site_idCAC
Number of Residues4
DetailsCATALYTIC SITE. HIS 8 PHOSPHORYLATION IS REQUIRED TO PRIME THE ENZYME.
ChainResidue
CHIS181
CARG7
CGLU86
CHIS8

site_idCAD
Number of Residues4
DetailsCATALYTIC SITE. HIS 8 PHOSPHORYLATION IS REQUIRED TO PRIME THE ENZYME.
ChainResidue
DHIS8
DHIS181
DARG7
DGLU86

Functional Information from PROSITE/UniProt
site_idPS00175
Number of Residues10
DetailsPG_MUTASE Phosphoglycerate mutase family phosphohistidine signature. LvRHGQsEwN
ChainResidueDetails
DLEU5-ASN14

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Tele-phosphohistidine intermediate => ECO:0000269|PubMed:10064712, ECO:0000269|PubMed:10531478, ECO:0000269|PubMed:6115412, ECO:0000269|PubMed:9512715
ChainResidueDetails
DHIS8
CHIS8
AHIS8
BHIS8

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton donor/acceptor => ECO:0000305|PubMed:10064712
ChainResidueDetails
DGLU86
CGLU86
AGLU86
BGLU86

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10369755, ECO:0000269|PubMed:10531478, ECO:0000269|PubMed:6115412
ChainResidueDetails
DARG7
CARG7
AARG7
BARG7

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10369755, ECO:0000269|PubMed:10531478
ChainResidueDetails
DTHR20
CTHR20
ATHR20
BTHR20

site_idSWS_FT_FI5
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10531478
ChainResidueDetails
DARG59
CARG59
AARG59
BARG59

site_idSWS_FT_FI6
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:10369755, ECO:0000269|PubMed:6115412
ChainResidueDetails
DGLU86
DGLY182
CGLU86
CGLY182
AGLU86
AGLY182
BGLU86
BGLY182

site_idSWS_FT_FI7
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:10369755
ChainResidueDetails
DLYS97
DARG113
CLYS97
CARG113
ALYS97
AARG113
BLYS97
BARG113

site_idSWS_FT_FI8
Number of Residues4
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:10064712
ChainResidueDetails
DHIS181
CHIS181
AHIS181
BHIS181

site_idSWS_FT_FI9
Number of Residues8
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:17287358
ChainResidueDetails
DSER11
DSER184
CSER11
CSER184
ASER11
ASER184
BSER11
BSER184

site_idSWS_FT_FI10
Number of Residues4
DetailsMOD_RES: Phosphotyrosine => ECO:0007744|PubMed:19779198
ChainResidueDetails
DTYR48
CTYR48
ATYR48
BTYR48

site_idSWS_FT_FI11
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:17287358, ECO:0007744|PubMed:17330950, ECO:0007744|PubMed:18407956, ECO:0007744|PubMed:19779198
ChainResidueDetails
DSER115
CSER115
ASER115
BSER115

site_idSWS_FT_FI12
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:18407956
ChainResidueDetails
DSER126
CSER126
ASER126
BSER126

site_idSWS_FT_FI13
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:19779198
ChainResidueDetails
DSER127
CSER127
ASER127
BSER127

site_idSWS_FT_FI14
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:18407956, ECO:0007744|PubMed:19779198
ChainResidueDetails
DSER196
CSER196
ASER196
BSER196

site_idSWS_FT_FI15
Number of Residues28
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin) => ECO:0007744|PubMed:22106047
ChainResidueDetails
DLYS30
CLYS56
CLYS70
CLYS138
CLYS174
CLYS190
ALYS30
ALYS56
ALYS70
ALYS138
ALYS174
ALYS190
BLYS30
BLYS56
BLYS70
BLYS138
BLYS174
BLYS190
DLYS56
DLYS70
DLYS138
DLYS174
DLYS190
CLYS30

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1qhf
ChainResidueDetails
DHIS181
DHIS8
DGLU86
DARG59

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1qhf
ChainResidueDetails
CHIS181
CHIS8
CGLU86
CARG59

site_idCSA3
Number of Residues4
DetailsAnnotated By Reference To The Literature 1qhf
ChainResidueDetails
AHIS181
AHIS8
AGLU86
AARG59

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1qhf
ChainResidueDetails
BHIS181
BHIS8
BGLU86
BARG59

site_idMCSA1
Number of Residues4
DetailsM-CSA 504
ChainResidueDetails
DHIS8covalent catalysis
DARG59electrostatic stabiliser
DGLU86proton donor, proton shuttle (general acid/base)
DHIS181electrostatic stabiliser

site_idMCSA2
Number of Residues4
DetailsM-CSA 504
ChainResidueDetails
CHIS8covalent catalysis
CARG59electrostatic stabiliser
CGLU86proton donor, proton shuttle (general acid/base)
CHIS181electrostatic stabiliser

site_idMCSA3
Number of Residues4
DetailsM-CSA 504
ChainResidueDetails
AHIS8covalent catalysis
AARG59electrostatic stabiliser
AGLU86proton donor, proton shuttle (general acid/base)
AHIS181electrostatic stabiliser

site_idMCSA4
Number of Residues4
DetailsM-CSA 504
ChainResidueDetails
BHIS8covalent catalysis
BARG59electrostatic stabiliser
BGLU86proton donor, proton shuttle (general acid/base)
BHIS181electrostatic stabiliser

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PDB entries from 2024-07-24

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