Structure of PDB 2bfm Chain A Binding Site BS02
Receptor Information
>2bfm Chain A (length=266) Species:
5664
(Leishmania major) [
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VPVALVTGAAKRLGRSIAEGLHAEGYAVCLHYHRSAAEANALSATLNARR
PNSAITVQADLSNVATAPAPVTLFTRCAELVAACYTHWGRCDVLVNNASS
FYPTPLLRGDREAMETATADLFGSNAIAPYFLIKAFAHRVAGTPAKHRGT
NYSIINMVDAMTNQPLLGYTIYTMAKGALEGLTRSAALELAPLQIRVNGV
GPGLSVLVDDMPPAVWEGHRSKVPLYQRDSSAAEVSDVVIFLCSSKAKYI
TGTCVKVDGGYSLTRA
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
2bfm Chain A Residue 1290 [
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Receptor-Ligand Complex Structure
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PDB
2bfm
Structures of Leishmania Major Pteridine Reductase Complexes Reveal the Active Site Features Important for Ligand Binding and to Guide Inhibitor Design
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
F113 L188 Y194 L226 H241
Binding residue
(residue number reindexed from 1)
F101 L166 Y172 L204 H219
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R17 D181 Y194
Catalytic site (residue number reindexed from 1)
R12 D159 Y172
Enzyme Commision number
1.5.1.33
: pteridine reductase.
Gene Ontology
Molecular Function
GO:0004155
6,7-dihydropteridine reductase activity
GO:0016491
oxidoreductase activity
GO:0047040
pteridine reductase activity
Biological Process
GO:0006729
tetrahydrobiopterin biosynthetic process
GO:0031427
response to methotrexate
Cellular Component
GO:0005829
cytosol
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Cellular Component
External links
PDB
RCSB:2bfm
,
PDBe:2bfm
,
PDBj:2bfm
PDBsum
2bfm
PubMed
16055151
UniProt
Q01782
|PTR1_LEIMA Pteridine reductase 1 (Gene Name=PTR1)
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