2bpy: Difference between revisions

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[[Image:2bpy.jpg|left|200px]]
[[Image:2bpy.jpg|left|200px]]


{{Structure
<!--
|PDB= 2bpy |SIZE=350|CAPTION= <scene name='initialview01'>2bpy</scene>, resolution 1.9&Aring;
The line below this paragraph, containing "STRUCTURE_2bpy", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)  
|LIGAND= <scene name='pdbligand=3IN:N-[2(S)-CYCLOPENTYL-1(R)-HYDROXY-3(R)METHYL]-5-[(2(S)-TERTIARY-BUTYLAMINO-CARBONYL)-4-(N1-(2)-(N-METHYLPIPERAZINYL)-3-CHLORO-PYRAZINYL-5-CARBONYL)-PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYL-PENTANAMIDE'>3IN</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Deleted_entry Deleted entry], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.13.16 3.4.13.16] </span>
or leave the SCENE parameter empty for the default display.
|GENE= HIV-1 PROTEASE FROM THE NY5 ISOLATE ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=11676 Human immunodeficiency virus 1])
-->
|DOMAIN=
{{STRUCTURE_2bpy| PDB=2bpy  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2bpy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2bpy OCA], [http://www.ebi.ac.uk/pdbsum/2bpy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2bpy RCSB]</span>
}}


'''HIV-1 PROTEASE-INHIBITOR COMPLEX'''
'''HIV-1 PROTEASE-INHIBITOR COMPLEX'''
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[[Category: Chen, Z.]]
[[Category: Chen, Z.]]
[[Category: Munshi, S.]]
[[Category: Munshi, S.]]
[[Category: acid protease]]
[[Category: Acid protease]]
[[Category: hydrolase]]
[[Category: Hydrolase]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 20:37:54 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:09:58 2008''

Revision as of 20:37, 3 May 2008

File:2bpy.jpg

Template:STRUCTURE 2bpy

HIV-1 PROTEASE-INHIBITOR COMPLEX


OverviewOverview

The ability to replace an inhibitor bound to the HIV-1 protease in single crystals with other potent inhibitors offers the possibility of investigating a series of protease inhibitors rapidly and conveniently with the use of X-ray crystallography. This approach affords a fast turnaround of structural information for iterative rational drug designs and obviates the need for studying the complex structures by co-crystallization. The replacement approach has been successfully used with single crystals of the HIV-1 protease complexed with a weak inhibitor. The structures of the complexes obtained by the replacement method are similar to those determined by co-crystallization.

About this StructureAbout this Structure

2BPY is a Single protein structure of sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

ReferenceReference

Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme., Munshi S, Chen Z, Li Y, Olsen DB, Fraley ME, Hungate RW, Kuo LC, Acta Crystallogr D Biol Crystallogr. 1998 Sep 1;54(Pt 5):1053-60. PMID:9757136 Page seeded by OCA on Sat May 3 20:37:54 2008

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