7zir
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Cryo-EM structure of hnRNPDL amyloid fibrils
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Structural highlights
DiseaseHNRDL_HUMAN HNRNPDL-related limb-girdle muscular dystrophy D3. The disease is caused by variants affecting the gene represented in this entry. FunctionHNRDL_HUMAN Acts as a transcriptional regulator. Promotes transcription repression. Promotes transcription activation in differentiated myotubes (By similarity). Binds to double- and single-stranded DNA sequences. Binds to the transcription suppressor CATR sequence of the COX5B promoter (By similarity). Binds with high affinity to RNA molecules that contain AU-rich elements (AREs) found within the 3'-UTR of many proto-oncogenes and cytokine mRNAs. Binds both to nuclear and cytoplasmic poly(A) mRNAs. Binds to poly(G) and poly(A), but not to poly(U) or poly(C) RNA homopolymers. Binds to the 5'-ACUAGC-3' RNA consensus sequence.[1] See AlsoReferences | ||||||||||||||||||
This page was last modified 16:10, 13 December 2023.