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4QO8

Lactate Dehydrogenase A in complex with substituted 3-Hydroxy-2-mercaptocyclohex-2-enone compound 104

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004457molecular_functionlactate dehydrogenase activity
A0004459molecular_functionL-lactate dehydrogenase (NAD+) activity
A0005515molecular_functionprotein binding
A0005634cellular_componentnucleus
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006089biological_processlactate metabolic process
A0006096biological_processglycolytic process
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0019752biological_processcarboxylic acid metabolic process
A0035686cellular_componentsperm fibrous sheath
A0042802molecular_functionidentical protein binding
A0042867biological_processpyruvate catabolic process
A0045296molecular_functioncadherin binding
A0070062cellular_componentextracellular exosome
B0003824molecular_functioncatalytic activity
B0004457molecular_functionlactate dehydrogenase activity
B0004459molecular_functionL-lactate dehydrogenase (NAD+) activity
B0005515molecular_functionprotein binding
B0005634cellular_componentnucleus
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006089biological_processlactate metabolic process
B0006096biological_processglycolytic process
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0019752biological_processcarboxylic acid metabolic process
B0035686cellular_componentsperm fibrous sheath
B0042802molecular_functionidentical protein binding
B0042867biological_processpyruvate catabolic process
B0045296molecular_functioncadherin binding
B0070062cellular_componentextracellular exosome
C0003824molecular_functioncatalytic activity
C0004457molecular_functionlactate dehydrogenase activity
C0004459molecular_functionL-lactate dehydrogenase (NAD+) activity
C0005515molecular_functionprotein binding
C0005634cellular_componentnucleus
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005829cellular_componentcytosol
C0006089biological_processlactate metabolic process
C0006096biological_processglycolytic process
C0016020cellular_componentmembrane
C0016491molecular_functionoxidoreductase activity
C0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
C0019752biological_processcarboxylic acid metabolic process
C0035686cellular_componentsperm fibrous sheath
C0042802molecular_functionidentical protein binding
C0042867biological_processpyruvate catabolic process
C0045296molecular_functioncadherin binding
C0070062cellular_componentextracellular exosome
D0003824molecular_functioncatalytic activity
D0004457molecular_functionlactate dehydrogenase activity
D0004459molecular_functionL-lactate dehydrogenase (NAD+) activity
D0005515molecular_functionprotein binding
D0005634cellular_componentnucleus
D0005737cellular_componentcytoplasm
D0005739cellular_componentmitochondrion
D0005829cellular_componentcytosol
D0006089biological_processlactate metabolic process
D0006096biological_processglycolytic process
D0016020cellular_componentmembrane
D0016491molecular_functionoxidoreductase activity
D0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
D0019752biological_processcarboxylic acid metabolic process
D0035686cellular_componentsperm fibrous sheath
D0042802molecular_functionidentical protein binding
D0042867biological_processpyruvate catabolic process
D0045296molecular_functioncadherin binding
D0070062cellular_componentextracellular exosome
Functional Information from PDB Data
site_idAC1
Number of Residues28
DetailsBINDING SITE FOR RESIDUE NAI A 801
ChainResidue
AGLY28
AARG98
AILE115
AILE119
AVAL135
ASER136
AASN137
ASER160
AHIS192
ATHR247
AILE251
AALA29
A36U804
AHOH906
AHOH910
AHOH931
AHOH950
AHOH999
AHOH1004
AHOH1043
AHOH1073
AVAL30
AASP51
AVAL52
AILE53
ATHR94
AALA95
AGLY96

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EPE A 802
ChainResidue
ATRP147
AGLY151
APHE152
ALYS154
AHOH1075

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 803
ChainResidue
AARG170
AHIS185
AHOH935
AHOH940
AHOH1005
AHOH1051
CHIS185

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 36U A 804
ChainResidue
AASN137
AASP165
AARG168
AHIS192
AGLY193
AALA237
ATYR238
AILE241
ATHR247
ANAI801

site_idAC5
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAI B 801
ChainResidue
BGLY28
BALA29
BVAL30
BASP51
BVAL52
BILE53
BLYS56
BTHR94
BALA95
BGLY96
BALA97
BARG98
BGLN99
BILE115
BILE119
BVAL135
BASN137
BSER160
BLEU164
BHIS192
BTHR247
BILE251
BLAC803
BHOH901
BHOH903
BHOH905
BHOH925
BHOH944
BHOH952
BHOH1017
BHOH1058
BHOH1141

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EPE B 802
ChainResidue
ALYS283
BTRP147
BGLY151
BPRO153
BLYS154
BHOH1115

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE LAC B 803
ChainResidue
BGLN99
BARG105
BASN137
BARG168
BHIS192
BALA237
BTHR247
BNAI801

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 B 804
ChainResidue
BHOH986
BHOH1023
DHIS185
DHOH902
BARG170
BHIS185
BHOH940

site_idAC9
Number of Residues21
DetailsBINDING SITE FOR RESIDUE NAI C 801
ChainResidue
CGLY28
CALA29
CVAL30
CASP51
CVAL52
CILE53
CTHR94
CALA95
CGLY96
CILE115
CVAL135
CSER136
CASN137
CHIS192
CTHR247
C36U804
CHOH928
CHOH933
CHOH955
CHOH969
CHOH972

site_idBC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EPE C 802
ChainResidue
CTRP147
CGLY151
CPHE152
CPRO153
CLYS154

site_idBC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SO4 C 803
ChainResidue
ALEU182
AHIS185
AHOH1068
CARG170
CHIS185
CHOH932
CHOH934
CHOH1024
CHOH1029
CHOH1039

site_idBC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE 36U C 804
ChainResidue
CASN137
CASP165
CARG168
CHIS192
CGLY193
CALA237
CTYR238
CNAI801
CHOH1031

site_idBC4
Number of Residues24
DetailsBINDING SITE FOR RESIDUE NAI D 801
ChainResidue
CGLU101
DGLY28
DALA29
DVAL30
DASP51
DVAL52
DILE53
DTHR94
DALA95
DILE115
DILE119
DVAL135
DASN137
DSER160
DHIS192
DTHR247
D36U803
DHOH912
DHOH930
DHOH942
DHOH1001
DHOH1015
DHOH1043
DHOH1051

site_idBC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 D 802
ChainResidue
BHIS185
DARG170
DHIS185
DHOH901
DHOH911
DHOH937

site_idBC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE 36U D 803
ChainResidue
DASN137
DASP165
DARG168
DHIS192
DGLY193
DALA237
DTYR238
DILE241
DTHR247
DNAI801
DHOH1015

Functional Information from PROSITE/UniProt
site_idPS00064
Number of Residues7
DetailsL_LDH L-lactate dehydrogenase active site. LGEHGDS
ChainResidueDetails
ALEU189-SER195

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsActive site: {"description":"Proton acceptor"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues116
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"11276087","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues16
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsModified residue: {"description":"N-acetylalanine","evidences":[{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"MAR-2005","submissionDatabase":"UniProtKB","authors":["Bienvenut W.V."]}},{"source":"PubMed","id":"19413330","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"22223895","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues12
DetailsModified residue: {"description":"N6-succinyllysine; alternate","evidences":[{"source":"UniProtKB","id":"P06151","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues4
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"19690332","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues12
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues4
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues4
DetailsModified residue: {"description":"N6-acetyllysine; alternate","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues12
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"P06151","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI11
Number of Residues4
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"UniProtKB","id":"P06151","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI12
Number of Residues8
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"UniProtKB","id":"P04642","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI13
Number of Residues4
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"24275569","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI14
Number of Residues8
DetailsCross-link: {"description":"Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2); alternate","evidences":[{"source":"PubMed","id":"28112733","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

247947

PDB entries from 2026-01-21

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