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TargetGag-Pol polyprotein [489-587]
LigandBDBM821
Substrate/Competitorn/a
IC50<0.200000±n/a nM
Citation Munroe, JEShepherd, TAJungheim, LNHornback, WJHatch, SDMuesing, MAWiskerchen, MSu, KSCampanale, KMBaxter, AJColacino, JM Potent, orally bioavailable HIV-1 protease inhibitors containing noncoded D-amino acids Bioorg Med Chem Lett5:2897-902 (1995)  
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:
BDBM821
n/a
NameBDBM821
Synonyms:(3aR,6S,7aS)-N-tert-butyl-5-[(2R,3S)-2-hydroxy-3-[(2S)-3-(naphthalene-2-sulfonyl)-2-(2,2,2-trifluoroacetamido)propanamido]-4-phenylbutyl]-octahydrothieno[3,2-c]pyridine-6-carboxamide | Saquinavir/Nelfinavir deriv. 25
TypeSmall organic molecule
Emp. Form.C37H45F3N4O6S2
Mol. Mass.762.902
SMILES[H][C@]12CCS[C@@]1([H])C[C@H](N(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CS(=O)(=O)c1ccc3ccccc3c1)NC(=O)C(F)(F)F)C2)C(=O)NC(C)(C)C |r|
Structure
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