Structure of PDB 1boz Chain A Binding Site BS01
Receptor Information
>1boz Chain A (length=186) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
VGSLNCIVAVSQNMGIGKNGDLPWPPLRNEGRYFQRMTTTSSVEGKQNLV
IMGKKTWFSIPEKNRPLKGRINLVLSRELKEPPQGAHFLSRSLDDALKLT
EQPELANKVDMVWIVGGSSVYKEAMNHPGHLKLFVTRIMQDFESDTFFPE
IDLEKYKLLPEYPGVLSDVQEEKGIKYKFEVYEKND
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
1boz Chain A Residue 187 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1boz
Structure-based design and synthesis of lipophilic 2,4-diamino-6-substituted quinazolines and their evaluation as inhibitors of dihydrofolate reductases and potential antitumor agents.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
V8 A9 I16 G20 D21 L22 G53 K54 K55 T56 S59 L75 S76 R77 V115 G117 S118 S119 V120 E123
Binding residue
(residue number reindexed from 1)
V8 A9 I16 G20 D21 L22 G53 K54 K55 T56 S59 L75 S76 R77 V115 G117 S118 S119 V120 E123
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L22 E30
Catalytic site (residue number reindexed from 1)
L22 E30
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0000900
mRNA regulatory element binding translation repressor activity
GO:0003723
RNA binding
GO:0003729
mRNA binding
GO:0004146
dihydrofolate reductase activity
GO:0005542
folic acid binding
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
GO:0070402
NADPH binding
GO:1990825
sequence-specific mRNA binding
Biological Process
GO:0006729
tetrahydrobiopterin biosynthetic process
GO:0006730
one-carbon metabolic process
GO:0017148
negative regulation of translation
GO:0031103
axon regeneration
GO:0031427
response to methotrexate
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:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1boz
,
PDBe:1boz
,
PDBj:1boz
PDBsum
1boz
PubMed
9719595
UniProt
P00374
|DYR_HUMAN Dihydrofolate reductase (Gene Name=DHFR)
[
Back to BioLiP
]