8g4l: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

The entry ~~8g4l is ON HOLD until Paper Publication~~

==Cryo-EM structure of the human cardiac myosin filament==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[8g4l]] is a 123 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=8G4L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8G4L FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 6.4Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8g4l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8g4l OCA], [https://pdbe.org/8g4l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8g4l RCSB], [https://www.ebi.ac.uk/pdbsum/8g4l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8g4l ProSAT]</span></td></tr>

</table>

== Disease ==

[https://www.uniprot.org/uniprot/MYL3_HUMAN MYL3_HUMAN] Familial isolated hypertrophic cardiomyopathy. The disease is caused by mutations affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/MYL3_HUMAN MYL3_HUMAN] Regulatory light chain of myosin. Does not bind calcium.

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Craig R]]

[[Category: Dutta D]]

[[Category: Nguyen V]]

[[Category: Padron R]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 8g4l is ON HOLD  until Paper Publication
+==Cryo-EM structure of the human cardiac myosin filament==
+<StructureSection load='8g4l' size='340' side='right'caption='[[8g4l]], [[Resolution|resolution]] 6.40&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8g4l]] is a 123 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=8G4L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8G4L FirstGlance]. <br>
-Description:
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 6.4&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8g4l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8g4l OCA], [https://pdbe.org/8g4l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8g4l RCSB], [https://www.ebi.ac.uk/pdbsum/8g4l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8g4l ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[https://www.uniprot.org/uniprot/MYL3_HUMAN MYL3_HUMAN] Familial isolated hypertrophic cardiomyopathy. The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/MYL3_HUMAN MYL3_HUMAN] Regulatory light chain of myosin. Does not bind calcium.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Craig R]]
+[[Category: Dutta D]]
+[[Category: Nguyen V]]
+[[Category: Padron R]]