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4R68

Lactate Dehydrogenase in complex with inhibitor compound 31

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004459molecular_functionL-lactate dehydrogenase activity
A0005515molecular_functionprotein binding
A0005634cellular_componentnucleus
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006089biological_processlactate metabolic process
A0006090biological_processpyruvate 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
A0042802molecular_functionidentical protein binding
A0045296molecular_functioncadherin binding
A0070062cellular_componentextracellular exosome
A1990204cellular_componentoxidoreductase complex
B0003824molecular_functioncatalytic activity
B0004459molecular_functionL-lactate dehydrogenase activity
B0005515molecular_functionprotein binding
B0005634cellular_componentnucleus
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006089biological_processlactate metabolic process
B0006090biological_processpyruvate 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
B0042802molecular_functionidentical protein binding
B0045296molecular_functioncadherin binding
B0070062cellular_componentextracellular exosome
B1990204cellular_componentoxidoreductase complex
C0003824molecular_functioncatalytic activity
C0004459molecular_functionL-lactate dehydrogenase activity
C0005515molecular_functionprotein binding
C0005634cellular_componentnucleus
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005829cellular_componentcytosol
C0006089biological_processlactate metabolic process
C0006090biological_processpyruvate 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
C0042802molecular_functionidentical protein binding
C0045296molecular_functioncadherin binding
C0070062cellular_componentextracellular exosome
C1990204cellular_componentoxidoreductase complex
D0003824molecular_functioncatalytic activity
D0004459molecular_functionL-lactate dehydrogenase activity
D0005515molecular_functionprotein binding
D0005634cellular_componentnucleus
D0005737cellular_componentcytoplasm
D0005739cellular_componentmitochondrion
D0005829cellular_componentcytosol
D0006089biological_processlactate metabolic process
D0006090biological_processpyruvate 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
D0042802molecular_functionidentical protein binding
D0045296molecular_functioncadherin binding
D0070062cellular_componentextracellular exosome
D1990204cellular_componentoxidoreductase complex
Functional Information from PDB Data
site_idAC1
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NAI A 801
ChainResidue
AGLY28
AARG98
AILE115
AVAL135
AASN137
AHIS192
ATHR247
AW31803
AHOH903
AHOH916
AHOH942
AALA29
AHOH965
AHOH983
AHOH998
AHOH1000
AHOH1002
AHOH1036
AHOH1047
AHOH1062
AHOH1087
AHOH1102
AVAL30
AASP51
AVAL52
AILE53
ATHR94
AALA95
AGLY96

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EPE A 802
ChainResidue
ATRP147
AGLY151
APHE152
APRO153
ALYS154

site_idAC3
Number of Residues16
DetailsBINDING SITE FOR RESIDUE W31 A 803
ChainResidue
AARG105
ALEU108
AASN137
ALEU164
AASP165
AARG168
AHIS192
AGLY193
AASP194
AALA237
ATYR238
AILE241
ATHR247
ANAI801
AHOH1036
AHOH1099

site_idAC4
Number of Residues31
DetailsBINDING SITE FOR RESIDUE NAI B 801
ChainResidue
BGLY28
BALA29
BVAL30
BASP51
BILE53
BTHR94
BALA95
BGLY96
BARG98
BILE115
BILE119
BVAL135
BASN137
BHIS192
BTHR247
BILE251
BW31803
BHOH901
BHOH904
BHOH906
BHOH912
BHOH927
BHOH928
BHOH938
BHOH948
BHOH977
BHOH998
BHOH1094
BHOH1121
BHOH1122
DGLY102

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EPE B 802
ChainResidue
ALYS283
BTRP147
BGLY151
BPRO153
BLYS154

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE W31 B 803
ChainResidue
BNAI801
BARG105
BLEU108
BASN137
BLEU164
BASP165
BARG168
BHIS192
BGLY193
BASP194
BALA237
BTYR238
BILE241
BTHR247

site_idAC7
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NAI C 801
ChainResidue
CGLY28
CALA29
CVAL30
CASP51
CVAL52
CILE53
CTHR94
CALA95
CGLY96
CILE115
CILE119
CVAL135
CASN137
CHIS192
CTHR247
CILE251
CW31803
CHOH903
CHOH922
CHOH931
CHOH937
CHOH979
CHOH987
CHOH989
CHOH1011
CHOH1012

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EPE C 802
ChainResidue
CTRP147
CGLY151
CPHE152
CPRO153
CLYS154

site_idAC9
Number of Residues11
DetailsBINDING SITE FOR RESIDUE W31 C 803
ChainResidue
CASN137
CASP165
CARG168
CHIS192
CGLY193
CASP194
CALA237
CTYR238
CILE241
CTHR247
CNAI801

site_idBC1
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAI D 801
ChainResidue
DGLY28
DALA29
DVAL30
DASP51
DVAL52
DILE53
DTHR94
DALA95
DGLY96
DPHE118
DILE119
DVAL135
DASN137
DHIS192
DTHR247
DILE251
DW31802
DHOH904
DHOH914
DHOH932
DHOH953
DHOH956
DHOH986
DHOH998
DHOH1005
DHOH1017
DHOH1028
DHOH1034
DHOH1038
DHOH1041
DHOH1043
DHOH1157

site_idBC2
Number of Residues14
DetailsBINDING SITE FOR RESIDUE W31 D 802
ChainResidue
DGLN99
DLEU108
DASN137
DLEU164
DASP165
DARG168
DHIS192
DGLY193
DASP194
DALA237
DTYR238
DILE241
DTHR247
DNAI801

site_idBC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE EPE D 803
ChainResidue
ALYS242
ALEU243
ALYS244
AGLY245
BASP55
BLYS56
DALA97
DARG98
DGLU103
DARG111

site_idBC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 D 804
ChainResidue
BHIS185
DARG170
DHIS185
DHOH966
DHOH1012
DHOH1078
DHOH1107

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
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
AHIS192
BHIS192
CHIS192
DHIS192

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:11276087
ChainResidueDetails
CGLY28
CARG98
DGLY28
DARG98
BGLY28
AGLY28
AARG98
BARG98

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING:
ChainResidueDetails
BARG105
BASN137
BARG168
BTHR247
CARG105
CASN137
CARG168
CTHR247
DARG105
DASN137
DARG168
DTHR247
AARG105
AASN137
AARG168
ATHR247

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: N-acetylalanine => ECO:0000269|Ref.10, ECO:0007744|PubMed:19413330, ECO:0007744|PubMed:22223895
ChainResidueDetails
BALA1
CALA1
DALA1
AALA1

site_idSWS_FT_FI5
Number of Residues12
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P06151
ChainResidueDetails
BLYS117
BLYS317
CLYS4
CLYS117
CLYS317
DLYS4
DLYS117
DLYS317
ALYS4
ALYS117
ALYS317
BLYS4

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Phosphotyrosine => ECO:0007744|PubMed:19690332
ChainResidueDetails
BTYR9
CTYR9
DTYR9
ATYR9

site_idSWS_FT_FI7
Number of Residues12
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
BLYS80
BLYS125
CLYS13
CLYS80
CLYS125
DLYS13
DLYS80
DLYS125
BLYS13
ALYS13
ALYS80
ALYS125

site_idSWS_FT_FI8
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0007744|PubMed:23186163
ChainResidueDetails
BTHR17
CTHR17
DTHR17
ATHR17

site_idSWS_FT_FI9
Number of Residues4
DetailsMOD_RES: N6-acetyllysine; alternate => ECO:0007744|PubMed:19608861
ChainResidueDetails
BLYS56
CLYS56
DLYS56
ALYS56

site_idSWS_FT_FI10
Number of Residues12
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P06151
ChainResidueDetails
BLYS231
BLYS242
CLYS223
CLYS231
CLYS242
DLYS223
DLYS231
DLYS242
ALYS223
ALYS231
ALYS242
BLYS223

site_idSWS_FT_FI11
Number of Residues4
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:P06151
ChainResidueDetails
BTYR238
CTYR238
ATYR238
DTYR238

site_idSWS_FT_FI12
Number of Residues8
DetailsMOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:P04642
ChainResidueDetails
CTHR308
CTHR321
DTHR308
DTHR321
ATHR321
BTHR321
ATHR308
BTHR308

site_idSWS_FT_FI13
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569
ChainResidueDetails
ASER309
BSER309
CSER309
DSER309

site_idSWS_FT_FI14
Number of Residues8
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2); alternate => ECO:0007744|PubMed:28112733
ChainResidueDetails
CLYS56
DLYS56
ALYS56
BLYS56

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PDB entries from 2024-04-17

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