Search Count: 4
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Alternate Binding Site For The P1-P3 Group Of A Class Of Potent Hiv-1 Protease Inhibitors As A Result Of Concerted Structural Change In 80'S Loop.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2000-12-28 Classification: HYDROLASE Ligands: 3IN |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2000-12-28
Ligands: 3IN
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Alternate Binding Site For The P1-P3 Group Of A Class Of Potent Hiv-1 Protease Inhibitors As A Result Of Concerted Structural Change In 80'S Loop.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2000-12-28 Classification: HYDROLASE Ligands: MK1 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2000-12-28
Ligands: MK1
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Alternate Binding Site For The P1-P3 Group Of A Class Of Potent Hiv-1 Protease Inhibitors As A Result Of Concerted Structural Change In 80'S Loop.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2000-12-28 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ROC |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2000-12-28
Ligands: ROC
 |
Alternate Binding Site For The P1-P3 Group Of A Class Of Potent Hiv-1 Protease Inhibitors As A Result Of Concerted Structural Change In 80'S Loop.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2000-12-28 Classification: HYDROLASE Ligands: L75 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2000-12-28
Ligands: L75