Structure of PDB 3jw3 Chain B Binding Site BS02
Receptor Information
>3jw3 Chain B (length=165) Species:
1392
(Bacillus anthracis) [
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HHHMRVSFMVAMDENRVIGKDNNLPWRLPSELQYVKKTTMGHPLIMGRKN
YEAIGRPLPGRRNIIVTRNEGYHVEGCEVAHSVEEVFELCKNEEEIFIIG
GAQIYDLFLPYVDKLYITKIHHAFEGDTFFPEMDMTNWKEVFVEKGLTDE
KNPYTYYYHVYEKQQ
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
3jw3 Chain B Residue 208 [
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Receptor-Ligand Complex Structure
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PDB
3jw3
Mutational Studies into Trimethoprim Resistance in Bacillus anthracis Dihydrofolate Reductase
Resolution
2.57 Å
Binding residue
(original residue number in PDB)
M6 V7 A8 E28 V32 I51 I96
Binding residue
(residue number reindexed from 1)
M9 V10 A11 E31 V35 I54 I99
Annotation score
1
Binding affinity
BindingDB: Ki=24100nM,IC50=71000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
M6 L21 W23 E28 L29 V32 L55 I93 T115
Catalytic site (residue number reindexed from 1)
M9 L24 W26 E31 L32 V35 L58 I96 T118
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
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:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3jw3
,
PDBe:3jw3
,
PDBj:3jw3
PDBsum
3jw3
PubMed
UniProt
Q81R22
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