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3i6o
From Proteopedia
(Difference between revisions)
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| + | [[Image:3i6o.jpg|left|200px]] | ||
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| + | The line below this paragraph, containing "STRUCTURE_3i6o", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3i6o| PDB=3i6o | SCENE= }} | ||
| - | + | ===Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A=== | |
| - | Description: Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19746963}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19746963 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19746963}} | ||
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| + | ==About this Structure== | ||
| + | 3I6O is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Viruses Viruses]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3I6O OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19746963</ref><references group="xtra"/> | ||
| + | [[Category: HIV-1 retropepsin]] | ||
| + | [[Category: Viruses]] | ||
| + | [[Category: Chumanevich, A A.]] | ||
| + | [[Category: Kovalevsky, A Y.]] | ||
| + | [[Category: Wang, Y F.]] | ||
| + | [[Category: Weber, I T.]] | ||
| + | [[Category: Aid]] | ||
| + | [[Category: Aspartyl protease]] | ||
| + | [[Category: Hiv-1]] | ||
| + | [[Category: Hydrolase]] | ||
| + | [[Category: Macrocyclic ligand]] | ||
| + | [[Category: Protease inhibitor]] | ||
| + | [[Category: Wild type protease]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 30 09:12:39 2009'' | ||
Revision as of 07:12, 30 September 2009
Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A
Template:ABSTRACT PUBMED 19746963
About this Structure
3I6O is a 2 chains structure of sequences from Viruses. Full crystallographic information is available from OCA.
Reference
- Ghosh AK, Kulkarni S, Anderson DD, Hong L, Baldridge A, Wang YF, Chumanevich AA, Kovalevsky AY, Tojo Y, Masayuki A, Koh Y, Tang J, Weber IT, Mitsuya H. Design, Synthesis, Protein-Ligand X-ray Structure, and Biological Evaluation of a Series of Novel Macrocyclic Human Immunodeficiency Virus-1 Protease Inhibitors to Combat Drug Resistance. J Med Chem. 2009 Sep 11. PMID:19746963 doi:10.1021/jm900695w
Page seeded by OCA on Wed Sep 30 09:12:39 2009
