Structure of PDB 5eyh Chain A Binding Site BS03
Receptor Information
>5eyh Chain A (length=262) Species:
1280
(Staphylococcus aureus) [
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TDKTLQQIDKLICSWLKQIDNVIPQLIMEMTTETKRHRFDLVTNVDKQIQ
QQFQQFLATYFPEHQLLAEEKSNAMITNEINHLWIMDPIDGTANLVKQQE
DYCIILAYFYEGKPMLSYVYDYPHKKLYKAIRGEGAFCNGFKMEEPPSLK
LEDAIISFNAQVMNLDTVQDLFDASFSYRLVGACGLDSMRVAKGQFGAHI
NTNPKPWDIAAQFLFAELLNLKMTTLDGKAIDHLKGAPFIISNKACHETV
LKILNANGGYQK
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
5eyh Chain A Residue 306 [
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Receptor-Ligand Complex Structure
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PDB
5eyh
Structural elucidation of the NADP(H) phosphatase activity of staphylococcal dual-specific IMPase/NADP(H) phosphatase
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
F40 D88 D91 G92 N160 V163 A184 C185 N202 T203 N204 D209
Binding residue
(residue number reindexed from 1)
F39 D87 D90 G91 N159 V162 A183 C184 N201 T202 N203 D208
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)
E69 D87 I89 D90 T92 D208
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:5eyh
,
PDBe:5eyh
,
PDBj:5eyh
PDBsum
5eyh
PubMed
26894675
UniProt
Q2FVV7
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