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TargetEnoyl-acyl-carrier protein reductase
LigandBDBM50211890
Substrate/Competitorn/a
Meas. Tech.ChEMBL_436470 (CHEMBL904775)
Ki 7300±n/a nM
Citation Kumar, GParasuraman, PSharma, SKBanerjee, TKarmodiya, KSurolia, NSurolia, A Discovery of a rhodanine class of compounds as inhibitors of Plasmodium falciparum enoyl-acyl carrier protein reductase. J Med Chem50:2665-75 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Enoyl-acyl-carrier protein reductase
Name:Enoyl-acyl-carrier protein reductase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:49770.86
Organism:Plasmodium falciparum
Description:ChEMBL_795989
Residue:432
Sequence:
MNKISQRLLFLFLHFYTTVCFIQNNTQKTFHNVLQNEQIRGKEKAFYRKEKRENIFIGNK
MKHVHNMNNTHNNNHYMEKEEQDASNINKIKEENKNEDICFIAGIGDTNGYGWGIAKELS
KRNVKIIFGIWPPVYNIFMKNYKNGKFDNDMIIDKDKKMNILDMLPFDASFDTANDIDEE
TKNNKRYNMLQNYPIEDVANLIHQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSK
SSYSLISLCKYFVNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLAYHLG
RNYNIRINTISAGPLKSRAATAINKLNNTYENNTNQNKNRNSHDVHNIMNNSGEKEEKKN
SASQNYTFIDYAIEYSEKYAPLRQKLLSTDIGSVASFLLSRESRAITGQTIYVDNGLNIM
FLPDDIYRNENE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50211890
n/a
NameBDBM50211890
Synonyms:6-(5-(4-(hexyloxy)-3-methoxybenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)hexanoic acid | CHEMBL227647
TypeSmall organic molecule
Emp. Form.C23H31NO5S2
Mol. Mass.465.626
SMILESCCCCCCOc1ccc(\C=C2/SC(=S)N(CCCCCC(O)=O)C2=O)cc1OC
Structure
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