1lyy

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[[Image:1lyy.jpg|left|200px]]
[[Image:1lyy.jpg|left|200px]]
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{{Structure
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|PDB= 1lyy |SIZE=350|CAPTION= <scene name='initialview01'>1lyy</scene>, resolution 1.8&Aring;
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The line below this paragraph, containing "STRUCTURE_1lyy", creates the "Structure Box" on the page.
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|SITE=
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] </span>
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{{STRUCTURE_1lyy| PDB=1lyy | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1lyy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1lyy OCA], [http://www.ebi.ac.uk/pdbsum/1lyy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1lyy RCSB]</span>
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}}
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'''AMYLOIDOGENIC VARIANT (ASP67HIS) OF HUMAN LYSOZYME'''
'''AMYLOIDOGENIC VARIANT (ASP67HIS) OF HUMAN LYSOZYME'''
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[[Category: Blake, C C.F.]]
[[Category: Blake, C C.F.]]
[[Category: Sunde, M.]]
[[Category: Sunde, M.]]
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[[Category: beta-1,4-glycan-hydrolase]]
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[[Category: Beta-1,4-glycan-hydrolase]]
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[[Category: enzyme]]
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[[Category: Enzyme]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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Revision as of 21:26, 2 May 2008

Template:STRUCTURE 1lyy

AMYLOIDOGENIC VARIANT (ASP67HIS) OF HUMAN LYSOZYME


Overview

Tissue deposition of soluble proteins as amyloid fibrils underlies a range of fatal diseases. The two naturally occurring human lysozyme variants are both amyloidogenic, and are shown here to be unstable. They aggregate to form amyloid fibrils with transformation of the mainly helical native fold, observed in crystal structures, to the amyloid fibril cross-beta fold. Biophysical studies suggest that partly folded intermediates are involved in fibrillogenesis, and this may be relevant to amyloidosis generally.

About this Structure

1LYY is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis., Booth DR, Sunde M, Bellotti V, Robinson CV, Hutchinson WL, Fraser PE, Hawkins PN, Dobson CM, Radford SE, Blake CC, Pepys MB, Nature. 1997 Feb 27;385(6619):787-93. PMID:9039909 Page seeded by OCA on Sat May 3 00:26:11 2008

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