Literature DB >> 24817723

Expression, purification and crystallization of the SKICH domain of human TAX1BP1.

Yang Yang1, Guan Wang1, Xiaolan Huang2, Zhihua Du1.   

Abstract

TAX1BP1 is a highly conserved, pleiotropic protein that plays many essential functions in human cells, including negative regulation of inflammatory and antimicrobial responses mediated by NF-κB and IRF3 signaling, inhibition of apoptosis, transcriptional coactivation and autophagy etc. TAX1BP1 contains a SKICH domain at the N-terminus, three coiled-coil domains in the middle and two ubiquitin-binding zinc-finger motifs at the C-terminus. The SKICH domain and the linker sequence between the SKICH domain and the coiled-coil region mediate interaction with ubiquitin-like proteins of the LC3/GABARAP family, which are autophagosome markers. For structure determination of the SKICH domain of TAX1BP1, a protein construct (amino acids 15-148) corresponding to the SKICH domain plus the linker region was expressed, purified and crystallized. A native diffraction data set has been collected to 1.9 Å resolution. A molecular-replacement solution has been found by using the structure of the SKICH domain of NDP52, a paralog of TAX1BP1.

Entities:  

Keywords:  A20; IRF3; NF-κB; SKICH domain; TAX1BP1; autophagy receptor; innate immune signaling

Mesh:

Substances:

Year:  2014        PMID: 24817723      PMCID: PMC4014332          DOI: 10.1107/S2053230X14006396

Source DB:  PubMed          Journal:  Acta Crystallogr F Struct Biol Commun        ISSN: 2053-230X            Impact factor:   1.056


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