Structure of PDB 4h96 Chain A Binding Site BS01
Receptor Information
>4h96 Chain A (length=189) Species:
5476
(Candida albicans) [
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PNVAIIVAALKPALGIGYKGKMPWRLRKEIRYFKDVTTRTTKPNTRNAVI
MGRKTWESIPQKFRPLPDRLNIILSRSYENEIIDDNIIHASSIESSLNLV
SDVERVFIIGGAEIYNELINNSLVSHLLITEIEHPSPESIEMDTFLKFPL
ESWTKQPKSELQKFVGDTVLEDDIKEGDFTYNYTLWTRK
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
4h96 Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4h96
Structural analysis of the active sites of dihydrofolate reductase from two species of Candida uncovers ligand-induced conformational changes shared among species.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
V10 A11 I19 G23 K24 M25 R56 K57 T58 S78 R79 S94 I112 G114 A115 E116 I117
Binding residue
(residue number reindexed from 1)
V7 A8 I16 G20 K21 M22 R53 K54 T55 S75 R76 S91 I109 G111 A112 E113 I114
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)
M22 W24 E29 I30 F33 L66 V106 T130
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:4h96
,
PDBe:4h96
,
PDBj:4h96
PDBsum
4h96
PubMed
23375226
UniProt
P22906
|DYR_CANAX Dihydrofolate reductase (Gene Name=DFR1)
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