5y4d

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Current revision (17:44, 28 October 2024) (edit) (undo)
 
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5y4d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5y4d OCA], [https://pdbe.org/5y4d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5y4d RCSB], [https://www.ebi.ac.uk/pdbsum/5y4d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5y4d ProSAT]</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=5y4d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5y4d OCA], [https://pdbe.org/5y4d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5y4d RCSB], [https://www.ebi.ac.uk/pdbsum/5y4d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5y4d ProSAT]</span></td></tr>
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<scene name='76/763657/Xyz/1'>test PNG created with my Mac with 16.2.21and loaded into default Jmol on Proteopedia</scene>
 
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== Disease ==
== Disease ==
[https://www.uniprot.org/uniprot/ANK2_HUMAN ANK2_HUMAN] Romano-Ward syndrome. Long QT syndrome 4 (LQT4) [MIM:[https://omim.org/entry/600919 600919]: A heart disorder characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to exercise or emotional stress, and can present with a sentinel event of sudden cardiac death in infancy. Long QT syndrome type 4 shows many atypical features compared to classical long QT syndromes, including pronounced sinus bradycardia, polyphasic T waves and atrial fibrillation. Cardiac repolarization defects may be not as severe as in classical LQT syndromes and prolonged QT interval on EKG is not a consistent feature. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:12571597</ref> <ref>PMID:15178757</ref>
[https://www.uniprot.org/uniprot/ANK2_HUMAN ANK2_HUMAN] Romano-Ward syndrome. Long QT syndrome 4 (LQT4) [MIM:[https://omim.org/entry/600919 600919]: A heart disorder characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to exercise or emotional stress, and can present with a sentinel event of sudden cardiac death in infancy. Long QT syndrome type 4 shows many atypical features compared to classical long QT syndromes, including pronounced sinus bradycardia, polyphasic T waves and atrial fibrillation. Cardiac repolarization defects may be not as severe as in classical LQT syndromes and prolonged QT interval on EKG is not a consistent feature. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:12571597</ref> <ref>PMID:15178757</ref>

Current revision

Crystal Structure of AnkB Ankyrin Repeats in Complex with AnkR/AnkB Chimeric Autoinhibition Segment

PDB ID 5y4d

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Proteopedia Page Contributors and Editors (what is this?)

OCA, Joel L. Sussman

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