Structure of PDB 8u7y Chain B Binding Site BS02
Receptor Information
>8u7y Chain B (length=603) Species:
9606
(Homo sapiens) [
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WLRWVTQQFKTIEISLQEFKAALHSFFAERFFALFRSGTITLQELQEALT
SPMDKLKFLFQVYDIDDPDELRTVLQSCLRESAISLPDEKLDQLTLALFE
SADAGAITFEELRDELQRFVMENLTISAAHWTRAYWHNHRSQLFCLATYA
GLHVLLFGLAASAHRDLGASVMVAKGCGQCLNFDCSFIAVLMLRRCLTWL
RATWLAQVLPLDQNIQFHQLMGYVVVGLSLVHTVAHTVNFVLQAQGSASP
TGVALLLLLLLMFICSSSCIRRSGHFEVFYWTHLSYLLVWLLLIFHGPNF
WKWLLVPGILFFLEKAIGLAVSRMAAVCIMEVNLLPSKVTHLLIKRPPFF
HYRPGDYLYLNIPTIARYEWHPFTISSAPEQKDTIWLHIRSQGQWTNRLY
ESFKACNIKCYIDGPYGTPTRRIFASEHAVLIGAGIGITPFASILQSIMY
RHQKRKHTCPSCQHSWIEGVQDNMKLHKVDFIWINRDQRSFEWFVSLLTK
LEMDQAEEAQYGRFLELHMYMTSALKAIGLQMALDLLANKEKKDSITGLQ
TRTQPGRPDWSKVFQKVEKKGKVQVFFCGSPALAKVLKGHCEKFGFRFFQ
ENF
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
8u7y Chain B Residue 804 [
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Receptor-Ligand Complex Structure
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PDB
8u7y
Structural Basis of Human NOX5 Activation
Resolution
4.06 Å
Binding residue
(original residue number in PDB)
D262 I593 N594 R595 T631 R671 P672 S696 F719
Binding residue
(residue number reindexed from 1)
D212 I484 N485 R486 T522 R557 P558 S580 F603
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.6.3.-
Gene Ontology
Molecular Function
GO:0005509
calcium ion binding
GO:0015252
proton channel activity
GO:0016175
superoxide-generating NAD(P)H oxidase activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
GO:0050664
oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor
GO:0106292
superoxide-generating NADPH oxidase activity
Biological Process
GO:0001525
angiogenesis
GO:0001819
positive regulation of cytokine production
GO:0001935
endothelial cell proliferation
GO:0006915
apoptotic process
GO:0006952
defense response
GO:0034220
monoatomic ion transmembrane transport
GO:0042554
superoxide anion generation
GO:0043012
regulation of fusion of sperm to egg plasma membrane
GO:0061640
cytoskeleton-dependent cytokinesis
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005886
plasma membrane
GO:0043020
NADPH oxidase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8u7y
,
PDBe:8u7y
,
PDBj:8u7y
PDBsum
8u7y
PubMed
UniProt
Q96PH1
|NOX5_HUMAN NADPH oxidase 5 (Gene Name=NOX5)
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