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TargetIAG-nucleoside hydrolase
LigandBDBM50260480
Substrate/Competitorn/a
Meas. Tech.ChEMBL_531315 (CHEMBL989727)
Ki 4500000±n/a nM
Citation Goeminne, AMcNaughton, MBal, GSurpateanu, GVan Der Veken, PDe Prol, SVersées, WSteyaert, JHaemers, AAugustyns, K Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors. Eur J Med Chem43:315-26 (2008) [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:
BDBM50260480
n/a
NameBDBM50260480
Synonyms:(2R,3S,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-tetrahydro-2-furancarboxamide | CHEMBL455563
TypeSmall organic molecule
Emp. Form.C6H11NO5
Mol. Mass.177.1552
SMILESNC(=O)[C@@H]1O[C@H](CO)[C@H](O)[C@@H]1O |r|
Structure
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