Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetHypoxanthine-guanine phosphoribosyltransferase
LigandBDBM92358
Substrate/Competitorn/a
Meas. Tech.Inhbition Assay
pH7.6±0
Temperature310.15±0 K
Ki 385±40 nM
Citation Hazleton, KZHo, MCCassera, MBClinch, KCrump, DRRosario, IMerino, EFAlmo, SCTyler, PCSchramm, VL Acyclic Immucillin Phosphonates: Second-Generation Inhibitors of Plasmodium falciparum Hypoxanthine- Guanine-Xanthine Phosphoribosyltransferase. Chem Biol19:721-30 (2012) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  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:
BDBM92358
n/a
NameBDBM92358
Synonyms:HGXPRT Inhibitor, 3
TypeSmall organic molecule
Emp. Form.C10H14N4O5P
Mol. Mass.301.2163
SMILESOC[C@H](CCP([O-])([O-])=O)[NH2+]c1c[nH]c2c1nc[nH]c2=O |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: