2ckc: Difference between revisions

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-{{Seed}}
-[[Image:2ckc.png|left|200px]]
-<!--
+==Solution structures of the BRK domains of the human Chromo Helicase Domain 7 and 8, reveals structural similarity with GYF domain suggesting a role in protein interaction==
-The line below this paragraph, containing "STRUCTURE_2ckc", creates the "Structure Box" on the page.
+<StructureSection load='2ckc' size='340' side='right'caption='[[2ckc]]' scene=''>
-You may change the PDB parameter (which sets the PDB file loaded into the applet)
+== Structural highlights ==
-or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+<table><tr><td colspan='2'>[[2ckc]] 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=2CKC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CKC FirstGlance]. <br>
-or leave the SCENE parameter empty for the default display.
+</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=2ckc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ckc OCA], [https://pdbe.org/2ckc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ckc RCSB], [https://www.ebi.ac.uk/pdbsum/2ckc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ckc ProSAT]</span></td></tr>
-{{STRUCTURE_2ckc|  PDB=2ckc  |  SCENE=  }}
+</table>
+== Disease ==
+[https://www.uniprot.org/uniprot/CHD7_HUMAN CHD7_HUMAN] CHARGE syndrome;Normosmic congenital hypogonadotropic hypogonadism;Omenn syndrome;Kallmann syndrome. The disease is caused by variants affecting the gene represented in this entry.  Disease susceptibility is associated with variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/CHD7_HUMAN CHD7_HUMAN] Probable transcription regulator. Maybe involved in the in 45S precursor rRNA production.<ref>PMID:22646239</ref>
+== Evolutionary Conservation ==
+[[Image:Consurf_key_small.gif|200px|right]]
+Check<jmol>
+  <jmolCheckbox>
+    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/ck/2ckc_consurf.spt"</scriptWhenChecked>
+    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
+    <text>to colour the structure by Evolutionary Conservation</text>
+  </jmolCheckbox>
+</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2ckc ConSurf].
+<div style="clear:both"></div>
-===SOLUTION STRUCTURES OF THE BRK DOMAINS OF THE HUMAN CHROMO HELICASE DOMAIN 7 AND 8, REVEALS STRUCTURAL SIMILARITY WITH GYF DOMAIN SUGGESTING A ROLE IN PROTEIN INTERACTION===
+==See Also==
+*[[Chromodomain-helicase-DNA-binding protein 3D structures|Chromodomain-helicase-DNA-binding protein 3D structures]]
+*[[Helicase 3D structures|Helicase 3D structures]]
-==About this Structure==
+== References ==
-CKC is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CKC OCA].
+<references/>
+__TOC__
+</StructureSection>
 [[Category: Homo sapiens]]
-[[Category: Ab, E.]]
+[[Category: Large Structures]]
-[[Category: Daniels, M.]]
+[[Category: Ab E]]
-[[Category: Diercks, T.]]
+[[Category: Daniels M]]
-[[Category: Folkers, G E.]]
+[[Category: Diercks T]]
-[[Category: Jong, R N.De.]]
+[[Category: Folkers GE]]
-[[Category: Kaptein, R.]]
+[[Category: Kaptein R]]
-[[Category: Xiaoyun, J.]]
+[[Category: Xiaoyun J]]
-[[Category: Atp-binding]]
+[[Category: De Jong RN]]
-[[Category: Brk domain]]
-[[Category: Chromatin regulator]]
-[[Category: Chromatin remodeling]]
-[[Category: Disease mutation]]
-[[Category: Dna-binding]]
-[[Category: Helicase]]
-[[Category: Hydrolase]]
-[[Category: Nuclear protein]]
-[[Category: Nucleotide-binding]]
-[[Category: Phosphorylation]]
-[[Category: Protein-protein interaction]]
-[[Category: Transcription]]
-[[Category: Transcription elongation]]
-[[Category: Transcription regulation]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 21:36:36 2009''