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8a4j
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 8a4j is ON HOLD Authors: Sutinen, A., Kursula, P. Description: Human GDAP1, A247V mutant Category: Unreleased Structures [[Category: Sutinen, A...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Human GDAP1, A247V mutant== | |
| - | + | <StructureSection load='8a4j' size='340' side='right'caption='[[8a4j]], [[Resolution|resolution]] 2.68Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8a4j]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8A4J OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8A4J FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.68Å</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8a4j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8a4j OCA], [https://pdbe.org/8a4j PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8a4j RCSB], [https://www.ebi.ac.uk/pdbsum/8a4j PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8a4j ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: Kursula | + | == Disease == |
| + | [https://www.uniprot.org/uniprot/GDAP1_HUMAN GDAP1_HUMAN] Charcot-Marie-Tooth disease type 2H;Autosomal recessive intermediate Charcot-Marie-Tooth disease type A;Autosomal dominant Charcot-Marie-Tooth disease type 2K;Autosomal recessive Charcot-Marie-Tooth disease with hoarseness;Charcot-Marie-Tooth disease type 4A. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by 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/GDAP1_HUMAN GDAP1_HUMAN] Regulates the mitochondrial network by promoting mitochondrial fission.<ref>PMID:16172208</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Kursula P]] | ||
| + | [[Category: Sutinen A]] | ||
Current revision
Human GDAP1, A247V mutant
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