Academic Journal

Molecular insights into the WW domain of the Golabi‐Ito‐Hall syndrome protein PQBP1

التفاصيل البيبلوغرافية
العنوان: Molecular insights into the WW domain of the Golabi‐Ito‐Hall syndrome protein PQBP1
المؤلفون: Sudol, Marius, McDonald, Caleb B., Farooq, Amjad
المصدر: FEBS Letters ; volume 586, issue 17, page 2795-2799 ; ISSN 0014-5793 1873-3468
بيانات النشر: Wiley
سنة النشر: 2012
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: The WW domain‐containing PQBP1 (polyglutamine tract‐binding protein 1) protein regulates mRNA processing and gene transcription. Mutations in the PQBP1 gene were reported in several X chromosome‐linked intellectual disability (XLID) disorders, including Golabi‐Ito‐Hall (GIH) syndrome. The missense mutation in the GIH syndrome maps within a functional region of the PQBP1 protein known as the WW domain. The causative mutation of PQBP1 replaces the conserved tyrosine (Y) at position 65 within the aromatic core of the WW domain to cysteine (C), which is a chemically significant change. In this short review, we analyze structural models of the Y65C mutated and wild type WW domains of PQBP1 in order to infer potential molecular mechanisms that render the mutated PQBP1 protein inactive in terms of ligand binding and its function as a regulator of mRNA splicing.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1016/j.febslet.2012.03.041
الاتاحة: http://dx.doi.org/10.1016/j.febslet.2012.03.041
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2Fj.febslet.2012.03.041
https://febs.onlinelibrary.wiley.com/doi/pdf/10.1016/j.febslet.2012.03.041
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
رقم الانضمام: edsbas.B5006581
قاعدة البيانات: BASE
الوصف
DOI:10.1016/j.febslet.2012.03.041