2cp3: Difference between revisions
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==Solution structure of the 2nd CAP-Gly domain in human CLIP-115/CYLN2== | ==Solution structure of the 2nd CAP-Gly domain in human CLIP-115/CYLN2== | ||
<StructureSection load='2cp3' size='340' side='right'caption='[[2cp3 | <StructureSection load='2cp3' size='340' side='right'caption='[[2cp3]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2cp3]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2cp3]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CP3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CP3 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2cp3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cp3 OCA], [https://pdbe.org/2cp3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2cp3 RCSB], [https://www.ebi.ac.uk/pdbsum/2cp3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2cp3 ProSAT], [https://www.topsan.org/Proteins/RSGI/2cp3 TOPSAN]</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=2cp3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cp3 OCA], [https://pdbe.org/2cp3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2cp3 RCSB], [https://www.ebi.ac.uk/pdbsum/2cp3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2cp3 ProSAT], [https://www.topsan.org/Proteins/RSGI/2cp3 TOPSAN]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/CLIP2_HUMAN CLIP2_HUMAN] Williams syndrome. CLIP2 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of CLIP2 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease. | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/CLIP2_HUMAN CLIP2_HUMAN] Seems to link microtubules to dendritic lamellar body (DLB), a membranous organelle predominantly present in bulbous dendritic appendages of neurons linked by dendrodendritic gap junctions. May operate in the control of brain-specific organelle translocations (By similarity). | |||
== 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: Inoue | [[Category: Inoue M]] | ||
[[Category: Kigawa | [[Category: Kigawa T]] | ||
[[Category: Koshiba | [[Category: Koshiba S]] | ||
[[Category: Saito K]] | |||
[[Category: Saito | [[Category: Yokoyama S]] | ||
[[Category: Yokoyama | |||