4fxj

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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fxj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fxj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4fxj RCSB], [http://www.ebi.ac.uk/pdbsum/4fxj PDBsum]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4fxj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fxj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4fxj RCSB], [http://www.ebi.ac.uk/pdbsum/4fxj PDBsum]</span></td></tr>
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== Function ==
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[[http://www.uniprot.org/uniprot/KPYM_HUMAN KPYM_HUMAN]] Glycolytic enzyme that catalyzes the transfer of a phosphoryl group from phosphoenolpyruvate (PEP) to ADP, generating ATP. Stimulates POU5F1-mediated transcriptional activation. Plays a general role in caspase independent cell death of tumor cells. The ratio betwween the highly active tetrameric form and nearly inactive dimeric form determines whether glucose carbons are channeled to biosynthetic processes or used for glycolytic ATP production. The transition between the 2 forms contributes to the control of glycolysis and is important for tumor cell proliferation and survival.<ref>PMID:17308100</ref> <ref>PMID:18191611</ref> <ref>PMID:21620138</ref>
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==

Revision as of 05:38, 25 December 2014

Structure of M2 pyruvate kinase in complex with phenylalanine

4fxj, resolution 2.90Å

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