2pwm: Difference between revisions

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


{{Structure
<!--
|PDB= 2pwm |SIZE=350|CAPTION= <scene name='initialview01'>2pwm</scene>, resolution 1.900&Aring;
The line below this paragraph, containing "STRUCTURE_2pwm", 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=CL:CHLORIDE+ION'>CL</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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or leave the SCENE parameter empty for the default display.
|GENE= gag-pol ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=11676 Human immunodeficiency virus 1])
-->
|DOMAIN=
{{STRUCTURE_2pwm|  PDB=2pwm |  SCENE= }}  
|RELATEDENTRY=[[2pwo|2PWO]], [[2pxr|2PXR]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2pwm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2pwm OCA], [http://www.ebi.ac.uk/pdbsum/2pwm PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2pwm RCSB]</span>
}}


'''Crystal Structure of HIV-1 CA146 A92E real cell'''
'''Crystal Structure of HIV-1 CA146 A92E real cell'''
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Kelly, B N.]]
[[Category: Kelly, B N.]]
[[Category: anti-viral]]
[[Category: Anti-viral]]
[[Category: hiv-1]]
[[Category: Hiv-1]]
[[Category: viral capsid]]
[[Category: Viral capsid]]
[[Category: viral protein]]
[[Category: Viral protein]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:41:41 2008''

Revision as of 13:55, 4 May 2008

File:2pwm.jpg

Template:STRUCTURE 2pwm

Crystal Structure of HIV-1 CA146 A92E real cell


OverviewOverview

The CA domain of the human immunodeficiency virus type 1 (HIV-1) Gag polyprotein plays critical roles in both the early and late phases of viral replication and is therefore an attractive antiviral target. Compounds with antiviral activity were recently identified that bind to the N-terminal domain of CA (CA N) and inhibit capsid assembly during viral maturation. We have determined the structure of the complex between CA N and the antiviral assembly inhibitor N-(3-chloro-4-methylphenyl)-N'-{2-[({5-[(dimethylamino)-methyl]-2-furyl}-m ethyl)-sulfanyl]ethyl}-urea) (CAP-1) using a combination of NMR spectroscopy and X-ray crystallography. The protein undergoes a remarkable conformational change upon CAP-1 binding, in which Phe32 is displaced from its buried position in the protein core to open a deep hydrophobic cavity that serves as the ligand binding site. The aromatic ring of CAP-1 inserts into the cavity, with the urea NH groups forming hydrogen bonds with the backbone oxygen of Val59 and the dimethylamonium group interacting with the side-chains of Glu28 and Glu29. Elements that could be exploited to improve binding affinity are apparent in the structure. The displacement of Phe32 by CAP-1 appears to be facilitated by a strained main-chain conformation, which suggests a potential role for a Phe32 conformational switch during normal capsid assembly.

About this StructureAbout this Structure

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

ReferenceReference

Structure of the antiviral assembly inhibitor CAP-1 complex with the HIV-1 CA protein., Kelly BN, Kyere S, Kinde I, Tang C, Howard BR, Robinson H, Sundquist WI, Summers MF, Hill CP, J Mol Biol. 2007 Oct 19;373(2):355-66. Epub 2007 Aug 15. PMID:17826792 Page seeded by OCA on Sun May 4 13:55:01 2008

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