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1ZX1

Human quinone oxidoreductase 2 (NQO2) in complex with the cytostatic prodrug CB1954

Functional Information from GO Data
ChainGOidnamespacecontents
A0001512molecular_functiondihydronicotinamide riboside quinone reductase activity
A0003955molecular_functionNAD(P)H dehydrogenase (quinone) activity
A0005515molecular_functionprotein binding
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0008270molecular_functionzinc ion binding
A0009055molecular_functionelectron transfer activity
A0016491molecular_functionoxidoreductase activity
A0016661molecular_functionoxidoreductase activity, acting on other nitrogenous compounds as donors
A0031404molecular_functionchloride ion binding
A0042803molecular_functionprotein homodimerization activity
A0046872molecular_functionmetal ion binding
A0070062cellular_componentextracellular exosome
A0071949molecular_functionFAD binding
A1901662biological_processquinone catabolic process
A1904408molecular_functionmelatonin binding
A1905594molecular_functionresveratrol binding
B0001512molecular_functiondihydronicotinamide riboside quinone reductase activity
B0003955molecular_functionNAD(P)H dehydrogenase (quinone) activity
B0005515molecular_functionprotein binding
B0005654cellular_componentnucleoplasm
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0008270molecular_functionzinc ion binding
B0009055molecular_functionelectron transfer activity
B0016491molecular_functionoxidoreductase activity
B0016661molecular_functionoxidoreductase activity, acting on other nitrogenous compounds as donors
B0031404molecular_functionchloride ion binding
B0042803molecular_functionprotein homodimerization activity
B0046872molecular_functionmetal ion binding
B0070062cellular_componentextracellular exosome
B0071949molecular_functionFAD binding
B1901662biological_processquinone catabolic process
B1904408molecular_functionmelatonin binding
B1905594molecular_functionresveratrol binding
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ZN A 231
ChainResidue
AHIS173
AHIS177
ACYS222

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ZN B 231
ChainResidue
BHIS173
BHIS177
BCYS222

site_idAC3
Number of Residues26
DetailsBINDING SITE FOR RESIDUE FAD A 232
ChainResidue
APHE17
AASN18
ASER20
APRO102
ALEU103
ATYR104
ATRP105
APHE106
ATHR147
ATHR148
AGLY149
AGLY150
ATYR155
AGLU197
AARG200
ALYS201
ACB1233
AHOH256
BASN66
BASP117
BHOH246
BHOH272
BHOH310
AHIS11
ALYS15
ASER16

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE CB1 A 233
ChainResidue
ATRP105
AGLY149
AGLY150
AMET154
AASN161
AFAD232
BPHE126
BPHE178
BHOH246

site_idAC5
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FAD B 234
ChainResidue
AASN66
AASP117
AHOH293
BHIS11
BLYS15
BSER16
BPHE17
BASN18
BSER20
BPRO102
BLEU103
BTYR104
BTRP105
BPHE106
BTHR147
BTHR148
BGLY149
BGLY150
BTYR155
BGLU193
BARG200
BCB1235
BHOH271

site_idAC6
Number of Residues9
DetailsBINDING SITE FOR RESIDUE CB1 B 235
ChainResidue
AILE128
APHE178
BTRP105
BPHE106
BGLY149
BGLY150
BMET154
BASN161
BFAD234

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:18254726, ECO:0000269|PubMed:19236722
ChainResidueDetails
AGLN12
BTYR104
BTHR148
BTHR156
BILE194
BLYS201
AASN18
ATYR104
ATHR148
ATHR156
AILE194
ALYS201
BGLN12
BASN18

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING:
ChainResidueDetails
AASP127
AGLY174
APHE178
ATHR223
BASP127
BGLY174
BPHE178
BTHR223

site_idSWS_FT_FI3
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:19369195
ChainResidueDetails
ALEU80
AGLU197
BLEU80
BGLU197

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1d4a
ChainResidueDetails
ATYR155
AASN161
AGLY149

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1d4a
ChainResidueDetails
BTYR155
BASN161
BGLY149

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PDB entries from 2024-10-30

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