Structure of PDB 3k47 Chain A Binding Site BS02
Receptor Information
>3k47 Chain A (length=186) Species:
10090
(Mus musculus) [
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VRPLNCIVAVSQNMGIGKNGDLPWPPLRNEFKYFQRMTTTSSVEGKQNLV
IMGRKTWFSIPEKNRPLKDRINIVLSRELKEPPRGAHFLAKSLDDALRLI
EQPELASKVDMVWIVGGSSVYQEAMNQPGHLRLFVTRIMQEFESDTFFPE
IDLGKYKLLPEYPGVLSEVQEEKGIKYKFEVYEKKD
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
3k47 Chain A Residue 187 [
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Receptor-Ligand Complex Structure
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PDB
3k47
Design, synthesis, and X-ray crystal structures of 2,4-diaminofuro[2,3-d]pyrimidines as multireceptor tyrosine kinase and dihydrofolate reductase inhibitors.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
V8 A9 I16 G17 D21 L22 G53 R54 K55 T56 L75 S76 R77 K91 S92 V115 G117 S118 S119 V120
Binding residue
(residue number reindexed from 1)
V8 A9 I16 G17 D21 L22 G53 R54 K55 T56 L75 S76 R77 K91 S92 V115 G117 S118 S119 V120
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L22 W24 E30 F31 F34 L67 M111 T136
Catalytic site (residue number reindexed from 1)
L22 W24 E30 F31 F34 L67 M111 T136
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0003723
RNA binding
GO:0003729
mRNA binding
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
GO:0051871
dihydrofolic acid binding
Biological Process
GO:0006729
tetrahydrobiopterin biosynthetic process
GO:0006730
one-carbon metabolic process
GO:0031103
axon regeneration
GO:0031427
response to methotrexate
GO:0035094
response to nicotine
GO:0035999
tetrahydrofolate interconversion
GO:0046452
dihydrofolate metabolic process
GO:0046653
tetrahydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic process
GO:0051000
positive regulation of nitric-oxide synthase activity
GO:2000121
regulation of removal of superoxide radicals
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3k47
,
PDBe:3k47
,
PDBj:3k47
PDBsum
3k47
PubMed
19748785
UniProt
P00375
|DYR_MOUSE Dihydrofolate reductase (Gene Name=Dhfr)
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