1exq: Difference between revisions
New page: left|200px<br /> <applet load="1exq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1exq, resolution 1.60Å" /> '''CRYSTAL STRUCTURE O... |
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[[Image:1exq.gif|left|200px]]<br /> | [[Image:1exq.gif|left|200px]]<br /><applet load="1exq" size="350" color="white" frame="true" align="right" spinBox="true" | ||
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caption="1exq, resolution 1.60Å" /> | caption="1exq, resolution 1.60Å" /> | ||
'''CRYSTAL STRUCTURE OF THE HIV-1 INTEGRASE CATALYTIC CORE DOMAIN'''<br /> | '''CRYSTAL STRUCTURE OF THE HIV-1 INTEGRASE CATALYTIC CORE DOMAIN'''<br /> | ||
==Overview== | ==Overview== | ||
Insolubility of full-length HIV-1 integrase (IN) limited previous | Insolubility of full-length HIV-1 integrase (IN) limited previous structure analyses to individual domains. By introducing five point mutations, we engineered a more soluble IN that allowed us to generate multidomain HIV-1 IN crystals. The first multidomain HIV-1 IN structure is reported. It incorporates the catalytic core and C-terminal domains (residues 52-288). The structure resolved to 2.8 A is a Y-shaped dimer. Within the dimer, the catalytic core domains form the only dimer interface, and the C-terminal domains are located 55 A apart. A 26-aa alpha-helix, alpha6, links the C-terminal domain to the catalytic core. A kink in one of the two alpha6 helices occurs near a known proteolytic site, suggesting that it may act as a flexible elbow to reorient the domains during the integration process. Two proteins that bind DNA in a sequence-independent manner are structurally homologous to the HIV-1 IN C-terminal domain, suggesting a similar protein-DNA interaction in which the IN C-terminal domain may serve to bind, bend, and orient viral DNA during integration. A strip of positively charged amino acids contributed by both monomers emerges from each active site of the dimer, suggesting a minimally dimeric platform for binding each viral DNA end. The crystal structure of the isolated catalytic core domain (residues 52-210), independently determined at 1.6-A resolution, is identical to the core domain within the two-domain 52-288 structure. | ||
==About this Structure== | ==About this Structure== | ||
1EXQ 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 CD, CL and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | 1EXQ 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 <scene name='pdbligand=CD:'>CD</scene>, <scene name='pdbligand=CL:'>CL</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EXQ OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Human immunodeficiency virus 1]] | [[Category: Human immunodeficiency virus 1]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Chen, J | [[Category: Chen, J C-H.]] | ||
[[Category: Finer-Moore, J | [[Category: Finer-Moore, J S.]] | ||
[[Category: Krucinski, J.]] | [[Category: Krucinski, J.]] | ||
[[Category: Leavitt, A | [[Category: Leavitt, A D.]] | ||
[[Category: Miercke, L | [[Category: Miercke, L J.W.]] | ||
[[Category: Stroud, R | [[Category: Stroud, R M.]] | ||
[[Category: Tang, A | [[Category: Tang, A H.]] | ||
[[Category: CD]] | [[Category: CD]] | ||
[[Category: CL]] | [[Category: CL]] | ||
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[[Category: polynucleotidyl transferase]] | [[Category: polynucleotidyl transferase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:32:38 2008'' |