Structure of PDB 4h97 Chain A Binding Site BS01
Receptor Information
>4h97 Chain A (length=190) Species:
5476
(Candida albicans) [
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KPNVAIIVAALKPALGIGYKGKMPWRLRKEIRYFKDVTTRTTKPNTRNAV
IMGRKTWESIPQKFRPLPDRLNIILSRSYENEIIDDNIIHASSIESSLNL
VSDVERVFIIGGAEIYNELINNSLVSHLLITEIEHPSPESIEMDTFLKFP
LESWTKQPKSELQKFVGDTVLEDDIKEGDFTYNYTLWTRK
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
4h97 Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4h97
Structural analysis of the active sites of dihydrofolate reductase from two species of Candida uncovers ligand-induced conformational changes shared among species.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
V10 A11 I19 G20 G23 K24 M25 G55 R56 K57 T58 L77 S78 R79 S94 I112 G114 A115 E116 I117
Binding residue
(residue number reindexed from 1)
V8 A9 I17 G18 G21 K22 M23 G53 R54 K55 T56 L75 S76 R77 S92 I110 G112 A113 E114 I115
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M25 W27 E32 I33 F36 L69 V109 T133
Catalytic site (residue number reindexed from 1)
M23 W25 E30 I31 F34 L67 V107 T131
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0046452
dihydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic process
Cellular Component
GO:0005739
mitochondrion
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4h97
,
PDBe:4h97
,
PDBj:4h97
PDBsum
4h97
PubMed
23375226
UniProt
P22906
|DYR_CANAX Dihydrofolate reductase (Gene Name=DFR1)
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