Structure of PDB 5eyg Chain B Binding Site BS03
Receptor Information
>5eyg Chain B (length=265) Species:
1280
(Staphylococcus aureus) [
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MTDKTLQQIDKLICSWLKQIDNVIPQLIMEMTTETKRHRFDLVTNVDKQI
QQQFQQFLATYFPEHQLLAEEKSNAMITNEINHLWIMDPIDGTANLVKQQ
EDYCIILAYFYEGKPMLSYVYDYPHKKLYKAIRGEGAFCNGFKMEEPPSL
KLEDAIISFNAQVMNLDTVQDLFDASFSYRLVGACGLDSMRVAKGQFGAH
INTNPKPWDIAAQFLFAELLNLKMTTLDGKAIDHLKGAPFIISNKACHET
VLKILNANGGYQKYR
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
5eyg Chain B Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
5eyg
Structural elucidation of the NADP(H) phosphatase activity of staphylococcal dual-specific IMPase/NADP(H) phosphatase
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
D91 G92 T93 A94 N160 V163 G183 C185 N202 T203 N204
Binding residue
(residue number reindexed from 1)
D91 G92 T93 A94 N160 V163 G183 C185 N202 T203 N204
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E70 D88 I90 D91 T93 D209
Catalytic site (residue number reindexed from 1)
E70 D88 I90 D91 T93 D209
Enzyme Commision number
3.1.3.25
: inositol-phosphate phosphatase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008934
inositol monophosphate 1-phosphatase activity
GO:0046872
metal ion binding
Biological Process
GO:0006020
inositol metabolic process
GO:0007165
signal transduction
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5eyg
,
PDBe:5eyg
,
PDBj:5eyg
PDBsum
5eyg
PubMed
26894675
UniProt
Q2FVV7
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