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1b5z
From Proteopedia
(Difference between revisions)
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<StructureSection load='1b5z' size='340' side='right'caption='[[1b5z]], [[Resolution|resolution]] 2.20Å' scene=''> | <StructureSection load='1b5z' size='340' side='right'caption='[[1b5z]], [[Resolution|resolution]] 2.20Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[1b5z]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[1b5z]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B5Z OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1B5Z FirstGlance]. <br> |
| - | </td></tr> | + | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1b5z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1b5z OCA], [https://pdbe.org/1b5z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1b5z RCSB], [https://www.ebi.ac.uk/pdbsum/1b5z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1b5z ProSAT]</span></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1b5z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1b5z OCA], [https://pdbe.org/1b5z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1b5z RCSB], [https://www.ebi.ac.uk/pdbsum/1b5z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1b5z ProSAT]</span></td></tr> | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/LYSC_HUMAN LYSC_HUMAN] Defects in LYZ are a cause of amyloidosis type 8 (AMYL8) [MIM:[https://omim.org/entry/105200 105200]; also known as systemic non-neuropathic amyloidosis or Ostertag-type amyloidosis. AMYL8 is a hereditary generalized amyloidosis due to deposition of apolipoprotein A1, fibrinogen and lysozyme amyloids. Viscera are particularly affected. There is no involvement of the nervous system. Clinical features include renal amyloidosis resulting in nephrotic syndrome, arterial hypertension, hepatosplenomegaly, cholestasis, petechial skin rash.<ref>PMID:8464497</ref> | |
== Function == | == Function == | ||
| - | + | [https://www.uniprot.org/uniprot/LYSC_HUMAN LYSC_HUMAN] Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents. | |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | + | [[Category: Fujii S]] | |
| - | [[Category: Fujii | + | [[Category: Funahashi J]] |
| - | [[Category: Funahashi | + | [[Category: Kubota M]] |
| - | [[Category: Kubota | + | [[Category: Takano K]] |
| - | [[Category: Takano | + | [[Category: Yamagata Y]] |
| - | [[Category: Yamagata | + | [[Category: Yutani K]] |
| - | [[Category: Yutani | + | |
| - | + | ||
| - | + | ||
| - | + | ||
Revision as of 09:32, 21 December 2022
CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS
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Categories: Homo sapiens | Large Structures | Fujii S | Funahashi J | Kubota M | Takano K | Yamagata Y | Yutani K

