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TargetEnoyl-acyl-carrier protein reductase
LigandBDBM50211905
Substrate/Competitorn/a
Meas. Tech.ChEMBL_436470 (CHEMBL904775)
Ki 14400±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
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  Blast E-value cutoff:
BDBM50211905
n/a
NameBDBM50211905
Synonyms:4-((3-(4-methoxyphenyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)benzaldehyde | CHEMBL228040
TypeSmall organic molecule
Emp. Form.C18H13NO3S2
Mol. Mass.355.431
SMILESCOc1ccc(cc1)N1C(=S)S\C(=C/c2ccc(C=O)cc2)C1=O
Structure
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