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{ <http://www.tkuhn.ch/bel2nanopub/RA1mbdP6m0cthhZfnfLzdkyj9WFgco_WtMYY4XEjMLL_U#_3> ?p ?o ?g. }
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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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