Structure of PDB 3qfx Chain A Binding Site BS02
Receptor Information
>3qfx Chain A (length=219) Species:
31286
(Trypanosoma brucei rhodesiense) [
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RPPLRPFSVVVASDEKGGIGDGGTIPWEIPEDMQYFRRVTTNLRGKNVKP
SPSKRNAVVMGRKTWDSLPPKFRPLSNRLNVVLSRSATKEQLLAGIPDPI
KRAEAANDVVAVNGGLEDALRMLVSKEHTSSIETVFCIGGGTIYKQALCA
PCVNVLQAIHRTVVRPASNSCSVFFDIPAAGTKTPEGLELVRESITDERV
STGAGGKKYQFEKLVPRNS
Ligand information
Ligand ID
CP6
InChI
InChI=1S/C12H13ClN4/c1-2-9-10(11(14)17-12(15)16-9)7-3-5-8(13)6-4-7/h3-6H,2H2,1H3,(H4,14,15,16,17)
InChIKey
WKSAUQYGYAYLPV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCc1c(c(nc(n1)N)N)c2ccc(cc2)Cl
ACDLabs 10.04
Clc2ccc(c1c(nc(nc1CC)N)N)cc2
CACTVS 3.341
CCc1nc(N)nc(N)c1c2ccc(Cl)cc2
Formula
C12 H13 Cl N4
Name
5-(4-CHLORO-PHENYL)-6-ETHYL-PYRIMIDINE-2,4-DIAMINE;
PYRIMETHAMINE
ChEMBL
CHEMBL36
DrugBank
DB00205
ZINC
ZINC000000057464
PDB chain
3qfx Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
3qfx
Trypanosomal dihydrofolate reductase reveals natural antifolate resistance
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
V32 V33 A34 D54 F58 T86 L90 I160
Binding residue
(residue number reindexed from 1)
V10 V11 A12 D32 F36 T64 L68 I138
Annotation score
1
Binding affinity
MOAD
: Ki=24.2nM
Enzymatic activity
Catalytic site (original residue number in PDB)
I47 D54
Catalytic site (residue number reindexed from 1)
I25 D32
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
2.1.1.45
: thymidylate synthase.
Gene Ontology
Molecular Function
GO:0004146
dihydrofolate reductase activity
GO:0050661
NADP binding
Biological Process
GO:0046654
tetrahydrofolate biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3qfx
,
PDBe:3qfx
,
PDBj:3qfx
PDBsum
3qfx
PubMed
21650210
UniProt
Q27783
|DRTS_TRYBB Bifunctional dihydrofolate reductase-thymidylate synthase
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