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TargetPhosphotransferase
LigandBDBM43830
Substrate/Competitorn/a
Meas. Tech.Inhibition Assay
Temperature298.15±0 K
Ki 1.05e+5± 2e+3 nM
IC50 4500000±0.0 nM
Citation Willson, MSanejouand, YHPerie, JHannaert, VOpperdoes, F Sequencing, modeling, and selective inhibition of Trypanosoma brucei hexokinase. Chem Biol9:839-47 (2002) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Phosphotransferase
Name:Phosphotransferase
Synonyms:Hexokinase
Type:Protein
Mol. Mass.:51306.14
Organism:Trypanosoma brucei
Description:Q38C42
Residue:471
Sequence:
MSRRLNNILEHISIQGNDGETVRAVKRDVAMAALTNQFTMSVESMRQIMTYLLYEMVEGL
EGRESTVRMLPSYVYKADPKRATGVFYALDLGGTNFRVLRVACKEGAVVDSSTSAFKIPK
YALEGNATDLFGFIASNVKKTMETRAPEDLNRTVPLGFTFSFPVEQTKVNRGVLIRWTKG
FSTKGVQGNDVIALLQAAFGRVSLKVNVVALCNDTVGTLISHYFKDPEVQVGVIIGTGSN
ACYFETASAVTKDPAVAARGSALTPINMESGNFDSKYRFVLPTTKFDLDIDDASLNKGQQ
ALEKMISGMYLGEIARRVIVHLSSINCLPAALQTALGNRGSFESRFAGMISADRMPGLQF
TRSTIQKVCGVDVQSIEDLRIIRDVCRLVRGRAAQLSASFCCAPLVKTQTQGRATIAIDG
SVFEKIPSFRRVLQDNINRILGPECDVRAVLAKDGSGIGAAFISAMVVNDK
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  Blast E-value cutoff:
BDBM43830
n/a
NameBDBM43830
Synonyms:5-(amoxymethyl)-3-[2-[(4-phenylthiazol-2-yl)hydrazono]propyl]tetrahydrofuran-2-one | 5-(pentoxymethyl)-3-[2-[(4-phenyl-1,3-thiazol-2-yl)hydrazinylidene]propyl]oxolan-2-one | 5-(pentoxymethyl)-3-[2-[(4-phenyl-2-thiazolyl)hydrazinylidene]propyl]-2-oxolanone | 5-Pentyloxymethyl-3-{2-[(4-phenyl-thiazol-2-yl)-hydrazono]-propyl}-dihydro-furan-2-one | Glucosamine derivative, 3 | MLS000557649 | SMR000174499 | cid_2865032
TypeSmall organic molecule
Emp. Form.C22H29N3O3S
Mol. Mass.415.549
SMILESCCCCCOCC1CC(CC(C)N=Nc2nc(cs2)-c2ccccc2)C(=O)O1 |w:13.12|
Structure
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