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2dnf
From Proteopedia
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==Solution structure of RSGI RUH-062, a DCX domain from human== | ==Solution structure of RSGI RUH-062, a DCX domain from human== | ||
| - | <StructureSection load='2dnf' size='340' side='right' caption='[[2dnf | + | <StructureSection load='2dnf' size='340' side='right'caption='[[2dnf]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2dnf]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2dnf]] 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=2DNF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2DNF 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'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2dnf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dnf OCA], [https://pdbe.org/2dnf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2dnf RCSB], [https://www.ebi.ac.uk/pdbsum/2dnf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2dnf ProSAT], [https://www.topsan.org/Proteins/RSGI/2dnf TOPSAN]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/DCDC2_HUMAN DCDC2_HUMAN] Defects in DCDC2 may be a cause of susceptibility to dyslexia type 2 (DYX2) [MIM:[https://omim.org/entry/600202 600202]; also known as specific reading disability type 2. Dyslexia is a relatively common, complex cognitive disorder that affects 5% to 10% of school-aged children. The disorder is characterized by an impairment of reading performance despite adequate motivational, educational and intellectual opportunities and in the absence of sensory or neurological disability.<ref>PMID:16278297</ref> |
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/DCDC2_HUMAN DCDC2_HUMAN] May be involved in neuronal migration during development of the cerebral neocortex (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: Hayashi | + | [[Category: Large Structures]] |
| - | [[Category: Hirota | + | [[Category: Hayashi F]] |
| - | [[Category: Nagashima | + | [[Category: Hirota H]] |
| - | [[Category: Ohashi | + | [[Category: Nagashima T]] |
| - | + | [[Category: Ohashi W]] | |
| - | [[Category: Yokoyama | + | [[Category: Yokoyama S]] |
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Current revision
Solution structure of RSGI RUH-062, a DCX domain from human
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