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1OO6

Nitroreductase from e-coli in complex with the dinitrobenzamide prodrug SN23862

Functional Information from GO Data
ChainGOidnamespacecontents
A0003955molecular_functionNAD(P)H dehydrogenase (quinone) activity
A0004155molecular_function6,7-dihydropteridine reductase activity
A0005829cellular_componentcytosol
A0010181molecular_functionFMN binding
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0042802molecular_functionidentical protein binding
A0042803molecular_functionprotein homodimerization activity
A0046256biological_process2,4,6-trinitrotoluene catabolic process
A0046857molecular_functionoxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor
B0003955molecular_functionNAD(P)H dehydrogenase (quinone) activity
B0004155molecular_function6,7-dihydropteridine reductase activity
B0005829cellular_componentcytosol
B0010181molecular_functionFMN binding
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0042802molecular_functionidentical protein binding
B0042803molecular_functionprotein homodimerization activity
B0046256biological_process2,4,6-trinitrotoluene catabolic process
B0046857molecular_functionoxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor
Functional Information from PDB Data
site_idAC1
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FMN A 218
ChainResidue
AARG10
ALYS205
AARG207
ASN2221
AHOH270
AHOH276
AHOH285
AHOH315
BPRO38
BSER39
BSER40
AHIS11
BTHR41
BASN42
BGLN142
BLEU145
ASER12
ALYS14
AASN71
APRO163
AILE164
AGLU165
AGLY166

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SN2 A 219
ChainResidue
ATHR41
AALA116
ALYS119
AGLY120
APHE124
BLYS14
BLYS74
BFMN220

site_idAC3
Number of Residues20
DetailsBINDING SITE FOR RESIDUE FMN B 220
ChainResidue
APRO38
ASER39
ASER40
AASN42
AGLN142
ALEU145
ASN2219
AHOH248
BARG10
BHIS11
BSER12
BLYS14
BLYS74
BPRO163
BILE164
BGLU165
BGLY166
BLYS205
BARG207
BHOH236

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SN2 A 221
ChainResidue
ALYS14
APHE70
AASN71
ALYS74
APHE199
AFMN218
AHOH301
AHOH315

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:11020276, ECO:0000269|PubMed:11491290, ECO:0000269|PubMed:15684426
ChainResidueDetails
AARG10
AGLU165
ALYS205
BARG10
BGLU165
BLYS205

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:Q01234
ChainResidueDetails
ALYS14
BTHR41
BASN71
BLYS74
BARG107
ATHR41
AASN71
ALYS74
AARG107
BLYS14

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 211
ChainResidueDetails
ALYS14electrostatic stabiliser, hydrogen bond donor
ALYS74electrostatic stabiliser, hydrogen bond donor
AGLU165electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues3
DetailsM-CSA 211
ChainResidueDetails
BLYS14electrostatic stabiliser, hydrogen bond donor
BLYS74electrostatic stabiliser, hydrogen bond donor
BGLU165electrostatic stabiliser, hydrogen bond donor

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건을2024-04-17부터공개중

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