9vxp: Difference between revisions

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'''Unreleased structure'''


The entry 9vxp is ON HOLD  until Paper Publication
==Cryo-EM structure of human Pyruvate kinase R (PK-R)==
 
<StructureSection load='9vxp' size='340' side='right'caption='[[9vxp]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
Authors: Ma, H.Y., Su, Z.M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9vxp]] is a 4 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=9VXP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9VXP FirstGlance]. <br>
Description: Cryo-EM structure of human Pyruvate kinase R (PK-R)
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.48&#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=9vxp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9vxp OCA], [https://pdbe.org/9vxp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9vxp RCSB], [https://www.ebi.ac.uk/pdbsum/9vxp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9vxp ProSAT]</span></td></tr>
[[Category: Ma, H.Y]]
</table>
[[Category: Su, Z.M]]
== Disease ==
[https://www.uniprot.org/uniprot/KPYR_HUMAN KPYR_HUMAN] Defects in PKLR are the cause of pyruvate kinase hyperactivity (PKHYP) [MIM:[https://omim.org/entry/102900 102900]; also known as high red cell ATP syndrome. This autosomal dominant phenotype is characterized by increase of red blood cell ATP.<ref>PMID:9090535</ref>  Defects in PKLR are the cause of pyruvate kinase deficiency of red cells (PKRD) [MIM:[https://omim.org/entry/266200 266200]. A frequent cause of hereditary non-spherocytic hemolytic anemia. Clinically, pyruvate kinase-deficient patients suffer from a highly variable degree of chronic hemolysis, ranging from severe neonatal jaundice and fatal anemia at birth, severe transfusion-dependent chronic hemolysis, moderate hemolysis with exacerbation during infection, to a fully compensated hemolysis without apparent anemia.
== Function ==
[https://www.uniprot.org/uniprot/KPYR_HUMAN KPYR_HUMAN] Plays a key role in glycolysis (By similarity).
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ma HY]]
[[Category: Su ZM]]
Retrieved from "https://proteopedia.org/9vxp"