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Results
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p(HGNC:HDAC4,pmod(S,K,559))
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Approximately 2000 hand curated statements drawn from 57 PubMeds.
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Copyright (c) 2011-2012, Selventa. All Rights Reserved.
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BEL Framework Small Corpus Document
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Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported License
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Thus Lys559, which lies within the N-terminal extension of class II HDACs, is required
for sumoylation of HDAC4 in vitro and in vivo and is likely to be the predominant
modification site for SUMO.
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Selventa
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2014-07-03T14:29:34.297+02:00
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