2cem: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 8: Line 8:


==About this Structure==
==About this Structure==
2CEM is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]] with 2AH as [[http://en.wikipedia.org/wiki/ligand ligand]]. Active as [[http://en.wikipedia.org/wiki/HIV-1_retropepsin HIV-1 retropepsin]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.16 3.4.23.16]]. Structure known Active Site: AC1. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2CEM OCA]].  
2CEM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1] with 2AH as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/HIV-1_retropepsin HIV-1 retropepsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.16 3.4.23.16] Structure known Active Site: AC1. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2CEM OCA].  


==Reference==
==Reference==
Line 30: Line 30:
[[Category: protease]]
[[Category: protease]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 17:05:58 2007''
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov  5 14:51:47 2007''

Revision as of 15:46, 5 November 2007

File:2cem.gif


2cem, resolution 1.8Å

Drag the structure with the mouse to rotate

P1' EXTENDED HIV-1 PROTEASE INHIBITORS ENCOMPASSING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMICKING SCAFFOLD

OverviewOverview

Two series of P1'-extended HIV-1 protease inhibitors comprising a tertiary, alcohol in the transition-state mimic exhibiting Ki values ranging from, 2.1 to 93 nM have been synthesized. Microwave-accelerated, palladium-catalyzed cross-couplings were utilized to rapidly optimize the, P1' side chain. High cellular antiviral potencies were encountered when, the P1' benzyl group was elongated with a 3- or 4-pyridyl substituent, (EC50 = 0.18-0.22 microM). X-ray crystallographic data were obtained for, three inhibitors cocrystallized with the enzyme.

About this StructureAbout this Structure

2CEM is a Single protein structure of sequence from Human immunodeficiency virus 1 with 2AH as ligand. Active as HIV-1 retropepsin, with EC number 3.4.23.16 Structure known Active Site: AC1. Full crystallographic information is available from OCA.

ReferenceReference

Microwave-accelerated synthesis of P1'-extended HIV-1 protease inhibitors encompassing a tertiary alcohol in the transition-state mimicking scaffold., Ekegren JK, Ginman N, Johansson A, Wallberg H, Larhed M, Samuelsson B, Unge T, Hallberg A, J Med Chem. 2006 Mar 9;49(5):1828-32. PMID:16509598

Page seeded by OCA on Mon Nov 5 14:51:47 2007

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA