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2cp3

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Current revision (11:28, 22 May 2024) (edit) (undo)
 
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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==
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<StructureSection load='2cp3' size='340' side='right'caption='[[2cp3]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
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<StructureSection load='2cp3' size='340' side='right'caption='[[2cp3]]' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[2cp3]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. 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>
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<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>
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</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">Kazusa cDNA fh25236 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
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</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 ==
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[[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.
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[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 ==
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[[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).
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[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>
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[[Category: Human]]
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Inoue, M]]
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[[Category: Inoue M]]
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[[Category: Kigawa, T]]
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[[Category: Kigawa T]]
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[[Category: Koshiba, S]]
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[[Category: Koshiba S]]
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[[Category: Structural genomic]]
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[[Category: Saito K]]
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[[Category: Saito, K]]
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[[Category: Yokoyama S]]
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[[Category: Yokoyama, S]]
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[[Category: Cyln2]]
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[[Category: Cytoskeleton associated protein]]
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[[Category: Kiaa0291]]
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[[Category: Microtubule binding]]
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[[Category: National project on protein structural and functional analyse]]
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[[Category: Nppsfa]]
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[[Category: Protein binding]]
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[[Category: Rsgi]]
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Current revision

Solution structure of the 2nd CAP-Gly domain in human CLIP-115/CYLN2

PDB ID 2cp3

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