1al1

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Revision as of 23:52, 24 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1al1" size="450" color="white" frame="true" align="right" spinBox="true" caption="1al1, resolution 2.7Å" /> '''CRYSTAL STRUCTURE OF ...)
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File:1al1.jpg


1al1, resolution 2.7Å

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CRYSTAL STRUCTURE OF ALPHA1: IMPLICATIONS FOR PROTEIN DESIGN

OverviewOverview

X-ray diffraction shows the structure of a synthetic protein model, formed, from noncovalent self-association of a 12-residue peptide and of sulfate, ions at low pH. This peptide is a fragment of a 16-residue polypeptide, that was designed to form an amphiphilic alpha helix with a ridge of Leu, residues along one helical face. By interdigitation of the leucines of, four such helices, the design called for self-association into a, four-alpha-helical bundle. The crystal structure (2.7 angstrom resolution;, R factor = 0.215) reveals a structure more complex than the design, with, both a tetramer and a hexamer. The alpha-helical tetramer with leucine, interior has more oblique crossing angles than most four-alpha-helical, bundles; the hexamer has a globular hydrophobic core of 12 leucine, residues and three associated sulfate ions. Computational analysis, suggests that the hexameric association is tighter than the tetrameric, one. The consistency of the structure with the design is discussed, as, well as the divergence.

About this StructureAbout this Structure

1AL1 is a Protein complex structure of sequences from [1] with SO4 and ACE as ligands. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of alpha 1: implications for protein design., Hill CP, Anderson DH, Wesson L, DeGrado WF, Eisenberg D, Science. 1990 Aug 3;249(4968):543-6. PMID:2382133

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