2jyg
From Proteopedia
(New page: 200px<br /><applet load="2jyg" size="350" color="white" frame="true" align="right" spinBox="true" caption="2jyg" /> '''Solution Structure of the W184A/M185A Mutant...) |
|||
Line 17: | Line 17: | ||
[[Category: Wong, H C.]] | [[Category: Wong, H C.]] | ||
[[Category: 3d-nmr]] | [[Category: 3d-nmr]] | ||
- | [[Category: | + | [[Category: aid]] |
[[Category: aspartyl protease]] | [[Category: aspartyl protease]] | ||
[[Category: capsid maturation]] | [[Category: capsid maturation]] | ||
Line 55: | Line 55: | ||
[[Category: zinc-finger]] | [[Category: zinc-finger]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Mar 14 09:42:58 2008'' |
Revision as of 07:42, 14 March 2008
|
Solution Structure of the W184A/M185A Mutant of the Carboxy-terminal Dimerization Domain of the HIV-1 Capsid Protein
Overview
As in other retroviruses, the HIV-1 capsid (CA) protein is composed of two domains, the N-terminal domain (NTD) and the C-terminal domain (CTD), joined by a flexible linker. The dimerization of the CTD is thought to be a critical step in the assembly of the immature and mature viral capsids. The precise nature of the functional form of CTD dimerization interface has been a subject of considerable interest. Previously, the CTD dimer was thought to involve a face-to-face dimerization observed in the early crystallographic studies. Recently, the crystallographic structure for a domain-swapped CTD dimer has been determined. This dimer, with an entirely different interface that includes the major homology region (MHR) has been suggested as the functional form during the Gag assembly. The structure determination of the monomeric wt CTD of HIV-1 has not been possible because of the monomer-dimer equilibrium in solution. We report the NMR structure of the [W184A/M185A]-CTD mutant in its monomeric form. These mutations interfere with dimerization without abrogating the assembly activity of Gag and CA. The NMR structure shows some important differences compared to the CTD structure in the face-to-face dimer. Notably, the helix-2 is much shorter, and the kink seen in the crystal structure of the wt CTD in the face-to-face dimer is absent. These NMR studies suggest that dimerization-induced conformational changes may be present in the two crystal structures of the CTD dimers and also suggest a mechanism that can simultaneously accommodate both of the distinctly different dimer models playing functional roles during the Gag assembly of the immature capsids.
About this Structure
2JYG is a Single protein structure of sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
Solution Structure of a Double Mutant of the Carboxy-Terminal Dimerization Domain of the HIV-1 Capsid Protein(,)., Wong HC, Shin R, Krishna NR, Biochemistry. 2008 Feb 26;47(8):2289-97. Epub 2008 Jan 26. PMID:18220423
Page seeded by OCA on Fri Mar 14 09:42:58 2008
Categories: Human immunodeficiency virus 1 | Single protein | Krishna, N R. | Shin, R. | Wong, H C. | 3d-nmr | Aid | Aspartyl protease | Capsid maturation | Capsid protein (ca) | Carboxy-terminal | Core protein | Ctd | Cytoplasm | Dimerization domain | Dna integration | Dna recombination | Dna-directed dna polymerase | Double mutant | Endonuclease | Hiv-1 | Hydrolase | Lipoprotein | Magnesium | Membrane | Metal-binding | Monomer structure | Multifunctional enzyme | Myristate | Nmr | Nuclease | Nucleotidyltransferase | Nucleus | Phosphoprotein | Protease | Rna-binding | Rna-directed dna polymerase | Transferase | Viral nucleoprotein | Viral protein | Virion | Zinc | Zinc-finger