Literature DB >> 19636966

NMR-assignments of a cytosolic domain of the C-terminus of polycystin-2.

Frank H Schumann1, Helen Hoffmeister, Maren Schmidt, Reto Bader, Elisabeth Besl, Ralph Witzgall, Hans Robert Kalbitzer.   

Abstract

Mutations in the PKD2 gene lead to the development of polycystic kidney disease (PKD). The PKD2 gene codes for polycystin-2, a cation channel with unknown function. The cytoplasmic, C-terminal domain interacts with a large number of proteins including mDia1, alpha-actinin, PIGEA-14, troponin, and tropomyosin. The C-terminal fragment polycystin-2 (680-796) consisting of 117 amino acids contains a putative calcium binding EF-hand. It was produced in Escherichia coli and enriched uniformly with (13)C and (15)N. The backbone and side chain resonances were assigned by multidimensional NMR methods, the obtained chemical shifts are typical for a partially folded protein. The chemical shifts obtained are in line with the existence of two paired helix-loop-helix (HLH) motifs.

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Year:  2009        PMID: 19636966     DOI: 10.1007/s12104-009-9160-x

Source DB:  PubMed          Journal:  Biomol NMR Assign        ISSN: 1874-270X            Impact factor:   0.746


  2 in total

1.  Polycystin-1 is required for stereocilia structure but not for mechanotransduction in inner ear hair cells.

Authors:  Katherine A Steigelman; Andrea Lelli; Xudong Wu; Jiangang Gao; Susan Lin; Klaus Piontek; Claas Wodarczyk; Alessandra Boletta; Hyunho Kim; Feng Qian; Gregory Germino; Gwenaëlle S G Géléoc; Jeffrey R Holt; Jian Zuo
Journal:  J Neurosci       Date:  2011-08-24       Impact factor: 6.167

2.  Ca2+-dependent conformational changes in a C-terminal cytosolic domain of polycystin-2.

Authors:  Frank Schumann; Helen Hoffmeister; Reto Bader; Maren Schmidt; Ralph Witzgall; Hans Robert Kalbitzer
Journal:  J Biol Chem       Date:  2009-06-22       Impact factor: 5.157

  2 in total

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