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1IE3

CRYSTAL STRUCTURE OF R153C E. COLI MALATE DEHYDROGENASE

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006096biological_processglycolytic process
A0006099biological_processtricarboxylic acid cycle
A0006108biological_processmalate metabolic process
A0006113biological_processfermentation
A0009061biological_processanaerobic respiration
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0016615molecular_functionmalate dehydrogenase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0019752biological_processcarboxylic acid metabolic process
A0019898cellular_componentextrinsic component of membrane
A0030060molecular_functionL-malate dehydrogenase (NAD+) activity
A0042803molecular_functionprotein homodimerization activity
B0003824molecular_functioncatalytic activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006096biological_processglycolytic process
B0006099biological_processtricarboxylic acid cycle
B0006108biological_processmalate metabolic process
B0006113biological_processfermentation
B0009061biological_processanaerobic respiration
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0016615molecular_functionmalate dehydrogenase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0019752biological_processcarboxylic acid metabolic process
B0019898cellular_componentextrinsic component of membrane
B0030060molecular_functionL-malate dehydrogenase (NAD+) activity
B0042803molecular_functionprotein homodimerization activity
C0003824molecular_functioncatalytic activity
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006096biological_processglycolytic process
C0006099biological_processtricarboxylic acid cycle
C0006108biological_processmalate metabolic process
C0006113biological_processfermentation
C0009061biological_processanaerobic respiration
C0016020cellular_componentmembrane
C0016491molecular_functionoxidoreductase activity
C0016615molecular_functionmalate dehydrogenase activity
C0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
C0019752biological_processcarboxylic acid metabolic process
C0019898cellular_componentextrinsic component of membrane
C0030060molecular_functionL-malate dehydrogenase (NAD+) activity
C0042803molecular_functionprotein homodimerization activity
D0003824molecular_functioncatalytic activity
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006096biological_processglycolytic process
D0006099biological_processtricarboxylic acid cycle
D0006108biological_processmalate metabolic process
D0006113biological_processfermentation
D0009061biological_processanaerobic respiration
D0016020cellular_componentmembrane
D0016491molecular_functionoxidoreductase activity
D0016615molecular_functionmalate dehydrogenase activity
D0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
D0019752biological_processcarboxylic acid metabolic process
D0019898cellular_componentextrinsic component of membrane
D0030060molecular_functionL-malate dehydrogenase (NAD+) activity
D0042803molecular_functionprotein homodimerization activity
Functional Information from PDB Data
site_idAC1
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NAD A 313
ChainResidue
AGLY7
AGLY78
AVAL79
AASN94
AILE117
ATHR118
AASN119
AVAL146
ALEU149
AHIS177
AALA223
AALA9
ATHR224
AMET227
AHOH328
AHOH336
AHOH344
AHOH352
AHOH358
AGLY10
AGLY11
AILE12
AASP34
AILE35
ASER76
AALA77

site_idAC2
Number of Residues24
DetailsBINDING SITE FOR RESIDUE NAD B 314
ChainResidue
BALA9
BGLY10
BGLY11
BILE12
BASP34
BILE35
BSER76
BALA77
BGLY78
BASN94
BILE97
BILE117
BTHR118
BASN119
BVAL121
BVAL146
BHIS177
BTHR224
BMET227
BHOH380
BHOH381
BHOH397
BHOH403
BHOH423

site_idAC3
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NAD C 315
ChainResidue
CGLY7
CALA9
CGLY10
CGLY11
CILE12
CASP34
CSER76
CALA77
CGLY78
CVAL79
CASN94
CILE97
CILE117
CTHR118
CASN119
CVAL121
CVAL146
CHIS177
CTHR224
CMET227
CHOH425
CHOH426
CHOH432
CHOH437
CHOH438
CHOH453

site_idAC4
Number of Residues21
DetailsBINDING SITE FOR RESIDUE NAD D 316
ChainResidue
DGLY7
DALA9
DGLY10
DGLY11
DILE12
DTYR33
DASP34
DILE35
DSER76
DALA77
DGLY78
DILE97
DILE117
DASN119
DVAL121
DVAL146
DHIS177
DALA223
DMET227
DHOH466
DHOH478

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PYR C 317
ChainResidue
CALA209
CGLY210
CHOH456
CILE206
CGLN207

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000305|PubMed:11389141
ChainResidueDetails
AHIS177
BHIS177
CHIS177
DHIS177

site_idSWS_FT_FI2
Number of Residues20
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000269|PubMed:11389141, ECO:0000269|PubMed:8331658
ChainResidueDetails
AGLY7
BMET227
CGLY7
CASP34
CASN94
CILE117
CMET227
DGLY7
DASP34
DASN94
DILE117
AASP34
DMET227
AASN94
AILE117
AMET227
BGLY7
BASP34
BASN94
BILE117

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000305|PubMed:1507230, ECO:0000305|PubMed:8331658
ChainResidueDetails
AARG81
CARG87
CASN119
CCYS153
DARG81
DARG87
DASN119
DCYS153
AARG87
AASN119
ACYS153
BARG81
BARG87
BASN119
BCYS153
CARG81

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
AHIS177
AASP150

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
BHIS177
BASP150

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
CHIS177
CASP150

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
DHIS177
DASP150

site_idCSA5
Number of Residues3
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
AHIS177
AASP150
ACYS153

site_idCSA6
Number of Residues3
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
BHIS177
BASP150
BCYS153

site_idCSA7
Number of Residues3
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
CHIS177
CASP150
CCYS153

site_idCSA8
Number of Residues3
DetailsAnnotated By Reference To The Literature 1emd
ChainResidueDetails
DHIS177
DASP150
DCYS153

site_idMCSA1
Number of Residues2
DetailsM-CSA 527
ChainResidueDetails
AASP150modifies pKa
AHIS177proton acceptor, proton donor

site_idMCSA2
Number of Residues2
DetailsM-CSA 527
ChainResidueDetails
BASP150modifies pKa
BHIS177proton acceptor, proton donor

site_idMCSA3
Number of Residues2
DetailsM-CSA 527
ChainResidueDetails
CASP150modifies pKa
CHIS177proton acceptor, proton donor

site_idMCSA4
Number of Residues2
DetailsM-CSA 527
ChainResidueDetails
DASP150modifies pKa
DHIS177proton acceptor, proton donor

237992

PDB entries from 2025-06-25

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