1lli
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(New page: 200px<br /><applet load="1lli" size="450" color="white" frame="true" align="right" spinBox="true" caption="1lli, resolution 2.100Å" /> '''THE CRYSTAL STRUCTU...)
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Revision as of 18:32, 20 November 2007
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THE CRYSTAL STRUCTURE OF A MUTANT PROTEIN WITH ALTERED BUT IMPROVED HYDROPHOBIC CORE PACKING
Overview
The dense packing observed in protein interiors appears to be crucial for, stabilizing the native structure--even subtle internal substitutions are, usually destabilizing. Thus, steric complementarity of core residues is, thought to be an important criterion for "inverse folding" predictive, methods, which judge whether a newly determined sequence is consistent, with any known folds. A major problem in the development of useful core, packing evaluation algorithms, however, is that there are occasional, mutations that are predicted to disrupt native packing but that yield an, equally or more stable protein. We have solved the crystal structure of, such a variant of lambda repressor, which, despite having three larger, core substitutions, is more stable than the wild type. The structure, reveals that the protein accommodates the potentially disruptive residues, with shifts in its alpha-helical arrangement. The variant is apparently, more stable because its packing is improved--the core has a higher packing, density and little geometric strain. These rearrangements, however, cause, repositioning of functional residues, which result in reduced DNA binding, activity. By comparing these results with the predictions of two core, packing algorithms, it is clear that the protein possesses a relatively, high degree of main-chain flexibility that must be accounted for in order, to predict the full spectrum of compatible core sequences. This study also, shows how, in protein evolution, a particular set of core residue, identities might be selected not because they provide optimal stability, but because they provide sufficient stability in addition to the precise, structure required for optimal activity.
About this Structure
1LLI is a Single protein structure of sequence from Enterobacteria phage lambda. Full crystallographic information is available from OCA.
Reference
The crystal structure of a mutant protein with altered but improved hydrophobic core packing., Lim WA, Hodel A, Sauer RT, Richards FM, Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):423-7. PMID:8278404
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