Literature DB >> 10084317

A novel glutamic acid to aspartic acid mutation near the end of the 2B rod domain in the keratin 1 chain in epidermolytic hyperkeratosis.

J M Yang1, K Nam, H C Kim, J H Lee, J K Park, K Wu, E S Lee, P M Steinert.   

Abstract

We report a mutation in a mild case of epidermolytic hyperkeratosis that results in a glutamic acid to aspartic acid substitution in a novel location, codon 477 or position 106 of the 2B rod domain of the keratin 1 chain. This residue has been conserved in all intermediate filament chains and lies near the beginning of the highly conserved helix termination sequence and just prior to the predicted molecular overlap region. Keratin filaments assembled in vitro from chains bearing this substitution are abnormal, indicating that the glutamic acid residue is critically involved in ionic interactions in intermediate levels of filament structure.

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Year:  1999        PMID: 10084317     DOI: 10.1038/sj.jid.5600439

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  2 in total

1.  Coiled-coil trigger motifs in the 1B and 2B rod domain segments are required for the stability of keratin intermediate filaments.

Authors:  K C Wu; J T Bryan; M I Morasso; S I Jang; J H Lee; J M Yang; L N Marekov; D A Parry; P M Steinert
Journal:  Mol Biol Cell       Date:  2000-10       Impact factor: 4.138

2.  In silico predicted structural and functional insights of all missense mutations on 2B domain of K1/K10 causing genodermatoses.

Authors:  Santasree Banerjee; Qian Wu; Yuyi Ying; Yanni Li; Matsuyuki Shirota; Dante Neculai; Chen Li
Journal:  Oncotarget       Date:  2016-08-16
  2 in total

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