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6BAD

Lactate Dehydrogenase in complex with inhibitor (R)-3-((2-chlorophenyl)thio)-6-(3-((4-fluorophenyl)amino)phenyl)-4-hydroxy-6-(thiophen-3-yl)-5,6-dihydro-2H-pyran-2-one

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 Residues28
Detailsbinding site for residue NAD A 801
ChainResidue
AGLY28
AALA97
AARG98
AILE115
AVAL135
ASER136
AASN137
AHIS192
ATHR247
AILE251
AHOH907
AALA29
AHOH917
AHOH926
AHOH927
AHOH945
AHOH971
AHOH981
AHOH1005
AHOH1011
AHOH1036
AVAL30
AASP51
AVAL52
AILE53
ATHR94
AALA95
AGLY96

site_idAC2
Number of Residues3
Detailsbinding site for residue EPE A 802
ChainResidue
ATRP147
AGLY151
ALYS154

site_idAC3
Number of Residues9
Detailsbinding site for residue EPE A 803
ChainResidue
AGLN99
AARG105
AASN137
APRO138
ATYR238
AD0Y805
AHOH956
AHOH961
AHOH1039

site_idAC4
Number of Residues7
Detailsbinding site for residue SO4 A 804
ChainResidue
AARG170
AHIS185
AHOH919
AHOH995
AHOH1004
CLEU182
CHIS185

site_idAC5
Number of Residues15
Detailsbinding site for residue D0Y A 805
ChainResidue
AARG98
AGLN99
AGLN100
AASN137
ALEU164
AASP165
AARG168
AHIS192
AGLY193
AALA237
ATYR238
AILE241
ATHR247
AEPE803
AHOH1048

site_idAC6
Number of Residues29
Detailsbinding site for residue NAD B 801
ChainResidue
BGLY28
BALA29
BVAL30
BASP51
BVAL52
BILE53
BLYS56
BTHR94
BALA95
BGLY96
BALA97
BARG98
BILE115
BILE119
BVAL135
BSER136
BASN137
BHIS192
BTHR247
BILE251
BHOH906
BHOH917
BHOH918
BHOH947
BHOH954
BHOH955
BHOH976
BHOH1002
DGLY102

site_idAC7
Number of Residues5
Detailsbinding site for residue EPE B 802
ChainResidue
ALYS283
BTRP147
BGLY151
BPRO153
BLYS154

site_idAC8
Number of Residues9
Detailsbinding site for residue EPE B 803
ChainResidue
BASN137
BPRO138
BTYR238
BD0Y805
BHOH915
BHOH970
BGLN99
BARG105
BLEU108

site_idAC9
Number of Residues7
Detailsbinding site for residue SO4 B 804
ChainResidue
BARG170
BHIS185
BHOH922
BHOH952
BHOH1000
BHOH1021
DHIS185

site_idAD1
Number of Residues15
Detailsbinding site for residue D0Y B 805
ChainResidue
BGLN99
BGLN100
BASN137
BLEU164
BASP165
BARG168
BHIS192
BGLY193
BASP194
BALA237
BTYR238
BILE241
BTHR247
BEPE803
BHOH970

site_idAD2
Number of Residues28
Detailsbinding site for residue NAD C 801
ChainResidue
CGLY28
CALA29
CVAL30
CASP51
CVAL52
CILE53
CLYS56
CTHR94
CALA95
CGLY96
CALA97
CARG98
CILE115
CVAL135
CSER136
CASN137
CHIS192
CTHR247
CILE251
CHOH905
CHOH910
CHOH916
CHOH938
CHOH939
CHOH944
CHOH960
CHOH989
CHOH1001

site_idAD3
Number of Residues4
Detailsbinding site for residue EPE C 802
ChainResidue
CTRP147
CGLY151
CPRO153
CLYS154

site_idAD4
Number of Residues9
Detailsbinding site for residue EPE C 803
ChainResidue
CGLN99
CARG105
CASN137
CPRO138
CTYR238
CD0Y807
CHOH975
CHOH979
CHOH1015

site_idAD5
Number of Residues3
Detailsbinding site for residue SO4 C 804
ChainResidue
CHIS214
CPRO215
CASP216

site_idAD6
Number of Residues6
Detailsbinding site for residue SO4 C 805
ChainResidue
AHIS185
CARG170
CHIS185
CHOH902
CHOH998
CHOH1017

site_idAD7
Number of Residues3
Detailsbinding site for residue EPE C 806
ChainResidue
CASP194
CGLU235
CTYR238

site_idAD8
Number of Residues14
Detailsbinding site for residue D0Y C 807
ChainResidue
CARG98
CGLN99
CGLN100
CASN137
CASP165
CARG168
CHIS192
CGLY193
CALA237
CTYR238
CILE241
CTHR247
CEPE803
CHOH979

site_idAD9
Number of Residues29
Detailsbinding site for residue NAD D 801
ChainResidue
DGLY28
DALA29
DVAL30
DASP51
DVAL52
DILE53
DLYS56
DTHR94
DALA95
DGLY96
DALA97
DARG98
DILE115
DVAL135
DSER136
DASN137
DHIS192
DTHR247
DILE251
DHOH906
DHOH918
DHOH926
DHOH931
DHOH935
DHOH945
DHOH946
DHOH968
DHOH983
DHOH999

site_idAE1
Number of Residues7
Detailsbinding site for residue SO4 D 802
ChainResidue
BHIS185
BHOH952
DARG170
DHIS185
DHOH908
DHOH920
DHOH1015

site_idAE2
Number of Residues13
Detailsbinding site for residue D0Y D 803
ChainResidue
DARG98
DGLN99
DARG105
DASN137
DASP165
DARG168
DHIS192
DGLY193
DALA237
DTYR238
DILE241
DTHR247
DHOH989

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
AGLY28
AARG98
BGLY28
BARG98
CGLY28
CARG98
DGLY28
DARG98

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

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

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

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

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

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

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

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

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

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

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
ALYS56
BLYS56
CLYS56
DLYS56

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PDB entries from 2024-07-10

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