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5KKA

E. coli malate dehydrogenase with the inhibitor 6DHNAD

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 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 activity
B0042803molecular_functionprotein homodimerization activity
Functional Information from PDB Data
site_idAC1
Number of Residues30
Detailsbinding site for residue 6V0 A 401
ChainResidue
AALA9
AGLY78
AASN94
AILE97
AASN100
ALEU101
AILE117
AASN119
AVAL121
AVAL146
AHIS177
AGLY10
AALA223
ATHR224
AMET227
AHOH509
AHOH538
AHOH548
AHOH560
AHOH589
AHOH612
AHOH625
AGLY11
AHOH675
AILE12
ATYR33
AASP34
AILE35
ASER76
AALA77

site_idAC2
Number of Residues30
Detailsbinding site for residue 6V0 B 401
ChainResidue
BGLY7
BGLY10
BGLY11
BILE12
BTYR33
BASP34
BILE35
BSER76
BALA77
BGLY78
BILE97
BASN100
BLEU101
BILE117
BASN119
BVAL121
BVAL146
BHIS177
BALA223
BTHR224
BMET227
BHOH518
BHOH532
BHOH538
BHOH553
BHOH569
BHOH575
BHOH594
BHOH605
BHOH653

Functional Information from PROSITE/UniProt
site_idPS00068
Number of Residues13
DetailsMDH Malate dehydrogenase active site signature. VTTLDiiRSntfV
ChainResidueDetails
AVAL146-VAL158

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000305|PubMed:11389141
ChainResidueDetails
AHIS177
BHIS177

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000269|PubMed:11389141, ECO:0000269|PubMed:8331658
ChainResidueDetails
AASN94
AILE117
AMET227
BGLY7
BASP34
BASN94
BILE117
BMET227
AGLY7
AASP34

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01516, ECO:0000305|PubMed:1507230, ECO:0000305|PubMed:8331658
ChainResidueDetails
BASN119
BARG153
AARG81
AARG87
AASN119
AARG153
BARG81
BARG87

Catalytic Information from CSA
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

221051

PDB entries from 2024-06-12

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