Structure of PDB 1vj3 Chain A Binding Site BS01
Receptor Information
>1vj3 Chain A (length=205) Species:
4754
(Pneumocystis carinii) [
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NQQKSLTLIVALTTSYGIGRSNSLPWKLKKEISYFKRVTSFVPTFDSFES
MNVVLMGRKTWESIPLQFRPLKGRINVVITRNESLDLGNGIHSAKSLDHA
LELLYRTYGSESSVQINRIFVIGGAQLYKAAMDHPKLDRIMATIIYKDIH
CDVFFPLKFRDKEWSSVWKKEKHSDLESWVGTKVPHGKINEDGFDYEFEM
WTRDL
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
1vj3 Chain A Residue 207 [
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Receptor-Ligand Complex Structure
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PDB
1vj3
Structural studies on bioactive compounds. 30. Crystal structure and molecular modeling studies on the Pneumocystis carinii dihydrofolate reductase cofactor complex with TAB, a highly selective antifolate.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
A12 I19 N23 S24 G58 R59 K60 T61 I80 T81 R82 I123 G125 A126 Q127 L128 Y129
Binding residue
(residue number reindexed from 1)
A11 I18 N22 S23 G57 R58 K59 T60 I79 T80 R81 I122 G124 A125 Q126 L127 Y128
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L25 E32
Catalytic site (residue number reindexed from 1)
L24 E31
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:1vj3
,
PDBe:1vj3
,
PDBj:1vj3
PDBsum
1vj3
PubMed
10736154
UniProt
P16184
|DYR_PNECA Dihydrofolate reductase
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