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TargetGag-Pol polyprotein [489-587]
LigandBDBM50069033
Substrate/Competitorn/a
Meas. Tech.ChEBML_80095
Ki 0.018000±n/a nM
Citation Rodgers, JDJohnson, BLWang, HErickson-Viitanen, SKlabe, RMBacheler, LCordova, BCChang, CH Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2' groups. Bioorg Med Chem Lett8:715-20 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Gag-Pol polyprotein [489-587]
Name:Gag-Pol polyprotein [489-587]
Synonyms:Human immunodeficiency virus type 1 protease | POL_HV1H2 | Pol polyprotein | gag-pol
Type:Enzyme Subunit
Mol. Mass.:10781.16
Organism:Human immunodeficiency virus type 1
Description:P04585[489-587]
Residue:99
Sequence:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50069033
n/a
NameBDBM50069033
Synonyms:(4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-1,3-bis-(3-methylamino-1H-indazol-5-ylmethyl)-[1,3]diazepan-2-one | CHEMBL434098
TypeSmall organic molecule
Emp. Form.C37H40N8O3
Mol. Mass.644.7653
SMILESCNc1[nH]nc2ccc(CN3[C@H](Cc4ccccc4)[C@H](O)[C@@H](O)[C@@H](Cc4ccccc4)N(Cc4ccc5n[nH]c(NC)c5c4)C3=O)cc12
Structure
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