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TargetIAG-nucleoside hydrolase
LigandBDBM50206267
Substrate/Competitorn/a
Meas. Tech.ChEMBL_438446 (CHEMBL886424)
Ki 5600000±n/a nM
Citation Goeminne, AMcNaughton, MBal, GSurpateanu, GVan der Veken, PDe Prol, SVersées, WSteyaert, JApers, SHaemers, AAugustyns, K 1,2,3-Triazolylalkylribitol derivatives as nucleoside hydrolase inhibitors. Bioorg Med Chem Lett17:2523-6 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
IAG-nucleoside hydrolase
Name:IAG-nucleoside hydrolase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:36316.77
Organism:Trypanosoma vivax
Description:ChEMBL_531315
Residue:327
Sequence:
MAKNVVLDHDGNLDDFVAMVLLASNTEKVRLIGALCTDADCFVENGFNVTGKIMCLMHNN
MNLPLFPIGKSAATAVNPFPKEWRCLAKNMDDMPILNIPENVELWDKIKAENEKYEGQQL
LADLVMNSEEKVTICVTGPLSNVAWCIDKYGEKFTSKVEECVIMGGAVDVRGNVFLPSTD
GTAEWNIYWDPASAKTVFGCPGLRRIMFSLDSTNTVPVRSPYVQRFGEQTNFLLSILVGT
MWAMCTHCELLRDGDGYYAWDALTAAYVVDQKVANVDPVPIDVVVDKQPNEGATVRTDAE
KYPLTFVARNPEAEFFLDMLLRSARAC
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50206267
n/a
NameBDBM50206267
Synonyms:(2S,3R,4S,5R)-2-(2-azidoethyl)-5-(hydroxymethyl)-tetrahydrofuran-3,4-diol | 3,6-Anhydro-1-azido-1,2-dideoxy-D-allo-heptitol | CHEMBL231630
TypeSmall organic molecule
Emp. Form.C7H13N3O4
Mol. Mass.203.1958
SMILESOC[C@H]1O[C@@H](CCN=[N+]=[N-])[C@H](O)[C@@H]1O |r|
Structure
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