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TargetGag-Pol polyprotein [489-587]
LigandBDBM50080117
Substrate/Competitorn/a
Meas. Tech.ChEBML_157695
Ki 0.011000±n/a nM
Citation Kaltenbach, RFKlabe, RMCordova, BCSeitz, SP Increased antiviral activity of cyclic urea HIV protease inhibitors by modifying the P1/P1' substituents. Bioorg Med Chem Lett9:2259-62 (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
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  Blast E-value cutoff:
BDBM50080117
n/a
NameBDBM50080117
Synonyms:(4R,5S,6S,7R)-1,3-Bis-(3-amino-1H-indazol-5-ylmethyl)-5,6-dihydroxy-4,7-bis-(3-methyl-benzyl)-[1,3]diazepan-2-one | CHEMBL70626
TypeSmall organic molecule
Emp. Form.C37H40N8O3
Mol. Mass.644.7653
SMILESCc1cccc(C[C@@H]2[C@H](O)[C@@H](O)[C@@H](Cc3cccc(C)c3)N(Cc3ccc4[nH]nc(N)c4c3)C(=O)N2Cc2ccc3[nH]nc(N)c3c2)c1
Structure
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