期刊
FEBS LETTERS
卷 580, 期 1, 页码 99-106出版社
WILEY
DOI: 10.1016/j.febslet.2005.11.076
关键词
PRYSPRY; crystal structure; FMF diseases; multiple wavelength anomalous dispersion
We determined the first structure of PRYSPRY, a domain found in over 500 different proteins, involved in innate immune signaling, cytokine signaling suppression, development, cell growth and retroviral restriction. The fold encompasses a 7-stranded and a 6-stranded antiparallel beta-sheet, arranged in a beta-sandwich. In the crystal, PRYSPRY forms a dimer where the C-terminus of an acceptor molecule binds to the concave surface of a donor molecule, which represents a putative interaction site. Mutations in the PRYSPRY domains of Pyrin, which are responsible for familial Mediterranean fever, map on the putative PRYSPRY interaction site. (c) 2005 Federation of European Biochemical Societies. Publised by Elsevier B.V. All rights reserved.
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