Structure of PDB 1nnu Chain B Binding Site BS02
Receptor Information
>1nnu Chain B (length=229) Species:
5833
(Plasmodium falciparum) [
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EDICFIAGIGDTNGYGWGIAKELSKRNVKIIFGIWPPVYNIFMKNYKNGK
FDNDMIIDKDKKMNILDMLPFDASFDTANDIDEETKNNKRYNMLQNYTIE
DVANLIHQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSKSSYSLI
SLCKYFVNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLA
YHLGRNYNIRINTISAGPLKSRAATAINK
Ligand information
Ligand ID
TCT
InChI
InChI=1S/C16H11ClO3/c17-12-3-6-16(15(19)9-12)20-14-5-2-10-7-13(18)4-1-11(10)8-14/h1-9,18-19H
InChIKey
JPSDMABQCFCGLC-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Oc1ccc2cc(Oc3ccc(Cl)cc3O)ccc2c1
OpenEye OEToolkits 1.5.0
c1cc(cc2c1cc(cc2)Oc3ccc(cc3O)Cl)O
ACDLabs 10.04
Clc3cc(O)c(Oc2cc1ccc(O)cc1cc2)cc3
Formula
C16 H11 Cl O3
Name
6-(4-CHLORO-2-HYDROXY-PHENOXY)-NAPHTHALEN-2-OL
ChEMBL
DrugBank
ZINC
ZINC000002047609
PDB chain
1nnu Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1nnu
Structural Elucidation of the Specificity of the Antibacterial Agent Triclosan for Malarial Enoyl Acyl Carrier Protein Reductase
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
A217 N218 A219 V222 Y267 Y277 A319 A320 I323
Binding residue
(residue number reindexed from 1)
A121 N122 A123 V126 Y171 Y181 A223 A224 I227
Annotation score
1
Binding affinity
MOAD
: Ki=0.15uM
Enzymatic activity
Catalytic site (original residue number in PDB)
Y277 K285
Catalytic site (residue number reindexed from 1)
Y181 K189
Enzyme Commision number
1.3.1.9
: enoyl-[acyl-carrier-protein] reductase (NADH).
Gene Ontology
Molecular Function
GO:0004318
enoyl-[acyl-carrier-protein] reductase (NADH) activity
Biological Process
GO:0006633
fatty acid biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1nnu
,
PDBe:1nnu
,
PDBj:1nnu
PDBsum
1nnu
PubMed
11792710
UniProt
Q9BH77
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