2f3k

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==Overview==
==Overview==
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In our previous crystallographic studies of human immunodeficiency virus, type 1 (HIV-1) protease-substrate complexes, we described a conserved, "envelope" that appears to be important for substrate recognition and the, selection of drug-resistant mutations. In this study, the complex of HIV-1, protease with the inhibitor RO1 was determined and comparison with the, substrate envelope provides a rationale for mutational patterns.
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In our previous crystallographic studies of human immunodeficiency virus type 1 (HIV-1) protease-substrate complexes, we described a conserved "envelope" that appears to be important for substrate recognition and the selection of drug-resistant mutations. In this study, the complex of HIV-1 protease with the inhibitor RO1 was determined and comparison with the substrate envelope provides a rationale for mutational patterns.
==About this Structure==
==About this Structure==
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[[Category: Cammack, N.]]
[[Category: Cammack, N.]]
[[Category: Heilek-Snyder, G.]]
[[Category: Heilek-Snyder, G.]]
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[[Category: King, N.M.]]
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[[Category: King, N M.]]
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[[Category: Nalivaika, E.A.]]
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[[Category: Nalivaika, E A.]]
[[Category: Prabu-Jeyabalan, M.]]
[[Category: Prabu-Jeyabalan, M.]]
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[[Category: Schiffer, C.A.]]
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[[Category: Schiffer, C A.]]
[[Category: PO4]]
[[Category: PO4]]
[[Category: RO1]]
[[Category: RO1]]
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[[Category: substrate envelope]]
[[Category: substrate envelope]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:24:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:17:23 2008''

Revision as of 15:17, 21 February 2008


2f3k, resolution 1.599Å

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Substrate envelope and drug resistance: crystal structure of r01 in complex with wild-type hiv-1 protease

Overview

In our previous crystallographic studies of human immunodeficiency virus type 1 (HIV-1) protease-substrate complexes, we described a conserved "envelope" that appears to be important for substrate recognition and the selection of drug-resistant mutations. In this study, the complex of HIV-1 protease with the inhibitor RO1 was determined and comparison with the substrate envelope provides a rationale for mutational patterns.

About this Structure

2F3K is a Single protein structure of sequence from Human immunodeficiency virus 1 with and as ligands. Active as HIV-1 retropepsin, with EC number 3.4.23.16 Full crystallographic information is available from OCA.

Reference

Substrate envelope and drug resistance: crystal structure of RO1 in complex with wild-type human immunodeficiency virus type 1 protease., Prabu-Jeyabalan M, King NM, Nalivaika EA, Heilek-Snyder G, Cammack N, Schiffer CA, Antimicrob Agents Chemother. 2006 Apr;50(4):1518-21. PMID:16569872

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