Structure of PDB 3hwr Chain B Binding Site BS01
Receptor Information
>3hwr Chain B (length=298) Species:
264198
(Cupriavidus pinatubonensis JMP134) [
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MKVAIMGAGAVGCYYGGMLARAGHEVILIARPQHVQAIEATGLRLETQSF
DEQVKVSASSDPSAVQGADLVLFCVKSTDTQSAALAMKPALAKSALVLSL
QNGVENADTLRSLLEQEVAAAVVYVATEMAGPGHVRHHGRGELVIEPTSH
GANLAAIFAAAGVPVETSDNVRGALWAKLILNCAYNALSAITQLPYGRLV
RGEGVEAVMRDVMEECFAVARAEGVKLPDDVALAIRRIAETMPRQSSSTA
QDLARGKRSEIDHLNGLIVRRGDALGIPVPANRVLHALVRLIEDKQQH
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
3hwr Chain B Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
3hwr
Crystal structure of PanE/ApbA family ketopantoate reductase (YP_299159.1) from Ralstonia eutropha JMP134 at 2.15 A resolution
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
M6 G7 G9 A10 V11 R31 V75 K76 N102 V125 A126 T127 E260
Binding residue
(residue number reindexed from 1)
M6 G7 G9 A10 V11 R31 V75 K76 N102 V125 A126 T127 E260
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K178
Catalytic site (residue number reindexed from 1)
K178
Enzyme Commision number
1.1.1.169
: 2-dehydropantoate 2-reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
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
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Cellular Component
External links
PDB
RCSB:3hwr
,
PDBe:3hwr
,
PDBj:3hwr
PDBsum
3hwr
PubMed
UniProt
Q46RB9
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