Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetHypoxanthine-guanine phosphoribosyltransferase
LigandBDBM50293832
Substrate/Competitorn/a
Meas. Tech.ChEMBL_572371 (CHEMBL1035272)
pH7.4±n/a
Ki>300000±n/a nM
Commentsextracted
Citation Keough, DTHocková, DHolý, ANaesens, LMSkinner-Adams, TSJersey, JGuddat, LW Inhibition of hypoxanthine-guanine phosphoribosyltransferase by acyclic nucleoside phosphonates: a new class of antimalarial therapeutics. J Med Chem52:4391-9 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Hypoxanthine-guanine phosphoribosyltransferase
Name:Hypoxanthine-guanine phosphoribosyltransferase
Synonyms:HGPRT | HGPRTase | HPRT | HPRT1 | HPRT_HUMAN | Hypoxanthine-guanine phosphoribosyltransferase | Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)
Type:Protein
Mol. Mass.:24579.61
Organism:Homo sapiens (Human)
Description:P00492
Residue:218
Sequence:
MATRSPGVVISDDEPGYDLDLFCIPNHYAEDLERVFIPHGLIMDRTERLARDVMKEMGGH
HIVALCVLKGGYKFFADLLDYIKALNRNSDRSIPMTVDFIRLKSYCNDQSTGDIKVIGGD
DLSTLTGKNVLIVEDIIDTGKTMQTLLSLVRQYNPKMVKVASLLVKRTPRSVGYKPDFVG
FEIPDKFVVGYALDYNEYFRDLNHVCVISETGKAKYKA
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50293832
n/a
NameBDBM50293832
Synonyms:((S)-1-(2-amino-8-bromo-6-oxo-1,6,7,8-tetrahydropurin-9-yl)propan-2-yloxy)methylphosphonate | CHEMBL555285
TypeSmall organic molecule
Emp. Form.C9H15BrN5O5P
Mol. Mass.384.124
SMILESC[C@@H](CN1C(Br)Nc2c1nc(N)[nH]c2=O)OCP(O)(O)=O |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: