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TargetGag-Pol polyprotein [489-587]
LigandBDBM810
Substrate/Competitorn/a
Meas. Tech.ChEMBL_157736 (CHEMBL765174)
Ki 0.12±n/a nM
Citation Tamamura, HKoh, YUeda, SSasaki, YYamasaki, TAoki, MMaeda, KWatai, YArikuni, HOtaka, AMitsuya, HFujii, N Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multidrug resistant HIV-1 strains. J Med Chem46:1764-8 (2003) [PubMed]  Article
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:
BDBM810
n/a
NameBDBM810
Synonyms:(3S,4aS,8aS)-N-tert-butyl-2-[(2R,3S)-2-hydroxy-3-[(2S)-2-methanesulfonamido-3-(naphthalene-2-sulfinyl)propanamido]-4-phenylbutyl]-decahydroisoquinoline-3-carboxamide | CHEMBL49002 | Saquinavir/Nelfinavir deriv. 14
TypeSmall organic molecule
Emp. Form.C38H52N4O6S2
Mol. Mass.724.973
SMILES[H][C@@]12CCCC[C@]1([H])CN(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CS(=O)c1ccc3ccccc3c1)NS(C)(=O)=O)[C@@H](C2)C(=O)NC(C)(C)C |r|
Structure
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