4i0c: Difference between revisions

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==The structure of the camelid antibody cAbHuL5 in complex with human lysozyme==
==The structure of the camelid antibody cAbHuL5 in complex with human lysozyme==
<StructureSection load='4i0c' size='340' side='right' caption='[[4i0c]], [[Resolution|resolution]] 1.95&Aring;' scene=''>
<StructureSection load='4i0c' size='340' side='right'caption='[[4i0c]], [[Resolution|resolution]] 1.95&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4i0c]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Arabian_camel Arabian camel] and [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4I0C OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4I0C FirstGlance]. <br>
<table><tr><td colspan='2'>[[4i0c]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Camelus_dromedarius Camelus dromedarius] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4I0C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4I0C FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">LYZ, LZM ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=4i0c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4i0c OCA], [https://pdbe.org/4i0c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4i0c RCSB], [https://www.ebi.ac.uk/pdbsum/4i0c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4i0c ProSAT]</span></td></tr>
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><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></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4i0c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4i0c OCA], [http://pdbe.org/4i0c PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4i0c RCSB], [http://www.ebi.ac.uk/pdbsum/4i0c PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4i0c ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/LYSC_HUMAN LYSC_HUMAN]] Defects in LYZ are a cause of amyloidosis type 8 (AMYL8) [MIM:[http://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>
[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 ==
[[http://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.  
[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.
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<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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==See Also==
==See Also==
*[[3D structures of antibody|3D structures of antibody]]
*[[Antibody 3D structures|Antibody 3D structures]]
*[[Lysozyme 3D structures|Lysozyme 3D structures]]
*[[3D structures of non-human antibody|3D structures of non-human antibody]]
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Arabian camel]]
[[Category: Camelus dromedarius]]
[[Category: Human]]
[[Category: Homo sapiens]]
[[Category: Lysozyme]]
[[Category: Large Structures]]
[[Category: Chan, P H]]
[[Category: Chan PH]]
[[Category: Chirgadze, D Y]]
[[Category: Chirgadze DY]]
[[Category: Christodoulou, J]]
[[Category: Christodoulou J]]
[[Category: Dobson, C M]]
[[Category: De Genst E]]
[[Category: Dumoulin, M]]
[[Category: Dobson CM]]
[[Category: Genst, E De]]
[[Category: Dumoulin M]]
[[Category: Kumita, J R]]
[[Category: Kumita JR]]
[[Category: Matagne, A]]
[[Category: Matagne A]]
[[Category: Menzer, L]]
[[Category: Menzer L]]
[[Category: Muyldermans, S]]
[[Category: Muyldermans S]]
[[Category: Pardon, E]]
[[Category: Pardon E]]
[[Category: Robinson, C V]]
[[Category: Robinson CV]]
[[Category: Wyns, L]]
[[Category: Wyns L]]
[[Category: Alpha-beta protein]]
[[Category: Beta-barrel]]
[[Category: Glycosidase]]
[[Category: Immune recognition]]
[[Category: Immune system-hydrolase complex]]

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