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TargetRibonuclease pancreatic
LigandBDBM50298711
Substrate/Competitorn/a
Meas. Tech.ChEMBL_588021 (CHEMBL1048356)
Ki 7000±n/a nM
Citation Debnath, JDasgupta, SPathak, T Nucleoside-amino acid conjugates: An alternative route to the design of ribonuclease A inhibitors. Bioorg Med Chem17:4921-7 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Ribonuclease pancreatic
Name:Ribonuclease pancreatic
Synonyms:CAM-RNase A | RNAS1_BOVIN | RNASE1 | RNAse A | RNS1
Type:Enzyme
Mol. Mass.:16468.79
Organism:Bison bison (American bison)
Description:carboxamidomethylated RNase A
Residue:150
Sequence:
MALKSLVLLSLLVLVLLLVRVQPSLGKETAAAKFERQHMDSSTSAASSSNYCNQMMKSRN
LTKDRCKPVNTFVHESLADVQAVCSQKNVACKNGQTNCYQSYSTMSITDCRETGSSKYPN
CAYKTTQANKHIIVACEGNPYVPVHFDASV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50298711
n/a
NameBDBM50298711
Synonyms:(2R,3R,4R,5R)-2-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-3-yl dihydrogen phosphate | CHEMBL582887 | CYTIDINE-2'-MONOPHOSPHATE
TypeSmall organic molecule
Emp. Form.C9H14N3O8P
Mol. Mass.323.1965
SMILESNc1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OP(O)(O)=O)c(=O)n1 |r|
Structure
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