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TargetEnoyl-acyl-carrier protein reductase
LigandBDBM50220547
Substrate/Competitorn/a
Meas. Tech.ChEMBL_457331 (CHEMBL941864)
Ki 800±n/a nM
Citation Tasdemir, DTopaloglu, BPerozzo, RBrun, RO'Neill, RCarballeira, NMZhang, XTonge, PJLinden, ARüedi, P Marine natural products from the Turkish sponge Agelas oroides that inhibit the enoyl reductases from Plasmodium falciparum, Mycobacterium tuberculosis and Escherichia coli. Bioorg Med Chem15:6834-45 (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:
BDBM50220547
n/a
NameBDBM50220547
Synonyms:4,5-Dibromo-1H-pyrrole-2-carboxylic acid [3-(2-amino-1H-imidazol-4-yl)-allyl]-amide | 4,5-Dibromo-1H-pyrrole-2-carboxylic acid [3-(2-amino-3H-imidazol-4-yl)-allyl]-amide | CHEMBL397591 | oroidin | oroidin base
TypeSmall organic molecule
Emp. Form.C11H11Br2N5O
Mol. Mass.389.046
SMILESNc1ncc(C=CCNC(=O)c2cc(Br)c(Br)[nH]2)[nH]1 |w:6.6|
Structure
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