6wqk
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hnRNPA2 Low complexity domain (LCD) determined by cryoEM
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Structural highlights
DiseaseROA2_HUMAN Inclusion body myopathy with Paget disease of bone and frontotemporal dementia. The disease is caused by mutations affecting the gene represented in this entry.[1] FunctionROA2_HUMAN Involved with pre-mRNA processing. Forms complexes (ribonucleosomes) with at least 20 other different hnRNP and heterogeneous nuclear RNA in the nucleus.X5DSL3_ANAMA See AlsoReferences
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This page was last modified 14:46, 6 March 2024.