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TitleA missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans.
Journal, issue, pagesNucleic Acids Res., Vol. 48, Page 9804-9821, Year 2020
Publish dateAug 8, 2019 (structure data deposition date)
AuthorsGrozdanov, P.N. / Masoumzadeh, E. / Kalscheuer, V.M. / Bienvenu, T. / Billuart, P. / Delrue, M.A. / Latham, M.P. / MacDonald, C.C.
External linksNucleic Acids Res. / PubMed:32816001
MethodsNMR (solution)
Structure data

PDB-6q2i:
Solution state NMR structures of the RNA recognition motif (RRM) domain of human CstF-64
Method: SOLUTION NMR

PDB-6tze:
Human CstF-64 RRM mutant - D50A
Method: SOLUTION NMR

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION / RNA recognition motif / RNA cleavage and polyadenylation / RNA BINDING PROTEIN

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