Structure of PDB 3n0h Chain A Binding Site BS02
Receptor Information
>3n0h Chain A (length=186) Species:
9606
(Homo sapiens) [
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VGSLNCIVAVSQNMGIGKNGDLPWPPLRNEFRYFSRMTTTSSVEGKQNLV
IMGKKTWFSIPEKFRPLKGRINLVLSRELKEPPQGAHFLSRSLDDALKLT
EQPELANKVDMVWIVGGSSVYKEAMNHPGHLKLFVTRIMQDFESDTFFPE
IDLEKYKLLPEYPGVLSDVQEEKGIKYKFEVYEKND
Ligand information
Ligand ID
TOP
InChI
InChI=1S/C14H18N4O3/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15/h5-7H,4H2,1-3H3,(H4,15,16,17,18)
InChIKey
IEDVJHCEMCRBQM-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC
OpenEye OEToolkits 1.5.0
COc1cc(cc(c1OC)OC)Cc2cnc(nc2N)N
ACDLabs 10.04
n1c(N)c(cnc1N)Cc2cc(OC)c(OC)c(OC)c2
Formula
C14 H18 N4 O3
Name
TRIMETHOPRIM
ChEMBL
CHEMBL22
DrugBank
DB00440
ZINC
ZINC000006627681
PDB chain
3n0h Chain A Residue 191 [
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Receptor-Ligand Complex Structure
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PDB
3n0h
Crystallographic analysis reveals a novel second binding site for trimethoprim in active site double mutants of human dihydrofolate reductase.
Resolution
1.92 Å
Binding residue
(original residue number in PDB)
S59 P61 F64
Binding residue
(residue number reindexed from 1)
S59 P61 F64
Annotation score
1
Binding affinity
MOAD
: Ki=617nM
PDBbind-CN
: -logKd/Ki=6.21,Ki=617nM
BindingDB: IC50=680000nM,Ki=19070nM
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3n0h
,
PDBe:3n0h
,
PDBj:3n0h
PDBsum
3n0h
PubMed
21684339
UniProt
P00374
|DYR_HUMAN Dihydrofolate reductase (Gene Name=DHFR)
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