Structure of PDB 4yca Chain B Binding Site BS01
Receptor Information
>4yca Chain B (length=286) Species:
1280
(Staphylococcus aureus) [
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LSVAIIGPGAVGTTIAYELQQSLPHTTLIGRHAKTITYYTVPHAPAQDIV
VKGYEDVTNTFDVIIIAVKTHQLDAVIPHLTYLAHEDTLIILAQNGYGQL
EHIPFKNVCQAVVYISGQKKGDVVTHFRDYQLRIQDNALTRQFRDLVQDS
QIDIVLEANIQQAIWYKLLVNLGINSITALGRQTVAIMHNPEIRILCRQL
LLDGCRVAQAEGLNFSEQTVDTIMTIYQGYPDEMGTSMYYDIVHQQPLEV
EAIQGFIYRRAREHNLDTPYLDTIYSFLRAYQQNEG
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/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/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
4yca Chain B Residue 800 [
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Receptor-Ligand Complex Structure
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PDB
4yca
Evidence of Kinetic Cooperativity in Dimeric Ketopantoate Reductase from Staphylococcus aureus.
Resolution
1.81 Å
Binding residue
(original residue number in PDB)
G9 P10 G11 A12 V13 R33 Y56 V70 Q74 V78 N97 V115 I117 S118 G119 K121 E251
Binding residue
(residue number reindexed from 1)
G7 P8 G9 A10 V11 R31 Y54 V68 Q72 V76 N95 V113 I115 S116 G117 K119 E249
Annotation score
4
Binding affinity
MOAD
: Kd=117nM
Enzymatic activity
Catalytic site (original residue number in PDB)
K169
Catalytic site (residue number reindexed from 1)
K167
Enzyme Commision number
1.1.1.169
: 2-dehydropantoate 2-reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004616
phosphogluconate dehydrogenase (decarboxylating) activity
GO:0008677
2-dehydropantoate 2-reductase activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0015940
pantothenate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4yca
,
PDBe:4yca
,
PDBj:4yca
PDBsum
4yca
PubMed
25946571
UniProt
A0A0J9X283
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