2on8: Difference between revisions

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[[Image:2on8.jpg|left|200px]]
[[Image:2on8.jpg|left|200px]]


{{Structure
<!--
|PDB= 2on8 |SIZE=350|CAPTION= <scene name='initialview01'>2on8</scene>, resolution 1.350&Aring;
The line below this paragraph, containing "STRUCTURE_2on8", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND=
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=
or leave the SCENE parameter empty for the default display.
|GENE= spg ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1306 Streptococcus sp.])
-->
|DOMAIN=
{{STRUCTURE_2on8|  PDB=2on8 |  SCENE= }}  
|RELATEDENTRY=[[1pga|1PGA]], [[1pgb|1PGB]], [[1gb4|1GB4]], [[1fcc|1FCC]], [[3gb1|3GB1]], [[1p7e|1P7E]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2on8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2on8 OCA], [http://www.ebi.ac.uk/pdbsum/2on8 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2on8 RCSB]</span>
}}


'''Gbeta1 stabilization by in vitro evolution and computational design'''
'''Gbeta1 stabilization by in vitro evolution and computational design'''
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[[Category: Heinemann, U.]]
[[Category: Heinemann, U.]]
[[Category: Max, K E.A.]]
[[Category: Max, K E.A.]]
[[Category: alpha helix]]
[[Category: Alpha helix]]
[[Category: beta sheet]]
[[Category: Beta sheet]]
[[Category: improved hydrophobic packing of core residue]]
[[Category: Improved hydrophobic packing of core residue]]
[[Category: protein binding]]
[[Category: Protein binding]]
 
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Revision as of 11:15, 4 May 2008

File:2on8.jpg

Template:STRUCTURE 2on8

Gbeta1 stabilization by in vitro evolution and computational design


OverviewOverview

Computational design and in vitro evolution are major strategies for stabilizing proteins. For the four critical positions 16, 18, 25, and 29 of the B domain of the streptococcal protein G (Gbeta1), they identified the same optimal residues at positions 16 and 25, but not at 18 and 29. Here we analyzed the energetic contributions of the residues from these two approaches by single and double mutant analyses and determined crystal structures for a variant from the calculation (I16/L18/E25/K29) and from the selection (I16/I18/E25/F29). The structural analysis explains the observed differences in stabilization. Residues 16, 18, and 29 line an invagination, which results from a packing defect between the helix and the beta-sheet of Gbeta1. In all stabilized variants, residues with larger side-chains occur at these positions and packing is improved. In the selected variant, packing is better optimized than in the computed variant. Such differences in side-chain packing strongly affect stability but are difficult to evaluate by computation.

About this StructureAbout this Structure

2ON8 is a Single protein structure of sequence from Streptococcus sp.. Full crystallographic information is available from OCA.

ReferenceReference

Optimization of the gbeta1 domain by computational design and by in vitro evolution: structural and energetic basis of stabilization., Wunderlich M, Max KE, Roske Y, Mueller U, Heinemann U, Schmid FX, J Mol Biol. 2007 Oct 26;373(3):775-84. Epub 2007 Aug 19. PMID:17868696 Page seeded by OCA on Sun May 4 11:15:24 2008

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