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2BC1

Structural Analysis of Streptococcus pyogenes NADH oxidase: C44S Nox

Functional Information from GO Data
ChainGOidnamespacecontents
A0008137molecular_functionNADH dehydrogenase (ubiquinone) activity
A0016491molecular_functionoxidoreductase activity
A1902600biological_processproton transmembrane transport
B0008137molecular_functionNADH dehydrogenase (ubiquinone) activity
B0016491molecular_functionoxidoreductase activity
B1902600biological_processproton transmembrane transport
Functional Information from PDB Data
site_idAC1
Number of Residues36
DetailsBINDING SITE FOR RESIDUE FAD A 457
ChainResidue
AVAL7
AGLY43
ASER44
AMET46
APRO80
AVAL81
AALA110
ATHR111
AGLY112
ASER113
AVAL142
AGLY8
ALYS143
ATYR170
AILE171
AGLY291
AASP292
AALA308
ALEU309
AALA310
ASER311
AHOH459
AASN10
AHOH463
AHOH464
AHOH593
AHOH609
BPHE436
BLEU437
BHOH468
AHIS11
AALA12
APHE33
AASP34
AGLN35
AASN36

site_idAC2
Number of Residues36
DetailsBINDING SITE FOR RESIDUE FAD B 457
ChainResidue
APHE436
ALEU437
BVAL7
BGLY8
BASN10
BHIS11
BALA12
BPHE33
BASP34
BGLN35
BGLY43
BSER44
BPRO80
BVAL81
BALA110
BTHR111
BGLY112
BSER113
BVAL142
BLYS143
BTYR170
BILE171
BPHE255
BGLY291
BASP292
BALA308
BLEU309
BALA310
BSER311
BHOH461
BHOH467
BHOH469
BHOH477
BHOH486
BHOH514
BHOH564

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000250|UniProtKB:P37062
ChainResidueDetails
AHIS11
BHIS11

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Redox-active => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0
ChainResidueDetails
ASER44
BSER44

site_idSWS_FT_FI3
Number of Residues22
DetailsBINDING: BINDING => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0, ECO:0007744|PDB:2BC1, ECO:0007744|PDB:2BCP
ChainResidueDetails
AASN10
AALA310
ASER311
BASN10
BALA12
BASP34
BGLN35
BVAL81
BSER113
BLYS143
BASP292
AALA12
BLEU309
BALA310
BSER311
AASP34
AGLN35
AVAL81
ASER113
ALYS143
AASP292
ALEU309

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0
ChainResidueDetails
ASER44
BSER44

site_idSWS_FT_FI5
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0, ECO:0007744|PDB:2BCP
ChainResidueDetails
AALA110
BALA110

site_idSWS_FT_FI6
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC1, ECO:0007744|PDB:2BCP
ChainResidueDetails
ATYR170
BTYR170

site_idSWS_FT_FI7
Number of Residues12
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P37062
ChainResidueDetails
AILE171
BGLY254
BALA308
BGLY339
AASP190
ATYR199
AGLY254
AALA308
AGLY339
BILE171
BASP190
BTYR199

site_idSWS_FT_FI8
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0, ECO:0007744|PDB:2BC1
ChainResidueDetails
APHE436
BPHE436

site_idSWS_FT_FI9
Number of Residues2
DetailsMOD_RES: Cysteine sulfinic acid (-SO2H) => ECO:0000269|PubMed:26506002, ECO:0007744|PDB:2BC0
ChainResidueDetails
ASER44
BSER44

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1get
ChainResidueDetails
AHIS439
ATYR444

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1get
ChainResidueDetails
BHIS439
BTYR444

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PDB entries from 2024-09-11

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