Literature DB >> 15941405

The CHiPS Domain--ancient traces for the Hermansky-Pudlak syndrome.

Marta Hoffman-Sommer1, Marcin Grynberg, Roza Kucharczyk, Joanna Rytka.   

Abstract

Hermansky-Pudlak syndrome (HPS) is a rare disorder caused by malfunctions of lysosomes and specialized lysosome-related organelles, resulting primarily in oculocutaneous albinism and bleeding diathesis. The majority of the HPS genes have been described as novel, but herein we report the identification of a conserved protein family which includes human HPS4, as well as distant homologs for other HPS genes. Our results suggest that the cellular machinery involved in the HPS syndrome is ancient.

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Year:  2005        PMID: 15941405     DOI: 10.1111/j.1600-0854.2005.00301.x

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


  9 in total

1.  Longin-like folds identified in CHiPS and DUF254 proteins: vesicle trafficking complexes conserved in eukaryotic evolution.

Authors:  Lisa N Kinch; Nick V Grishin
Journal:  Protein Sci       Date:  2006-11       Impact factor: 6.725

2.  Assembly of the biogenesis of lysosome-related organelles complex-3 (BLOC-3) and its interaction with Rab9.

Authors:  Daniel P Kloer; Raul Rojas; Viorica Ivan; Kengo Moriyama; Thijs van Vlijmen; Namita Murthy; Rodolfo Ghirlando; Peter van der Sluijs; James H Hurley; Juan S Bonifacino
Journal:  J Biol Chem       Date:  2010-01-04       Impact factor: 5.157

3.  A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).

Authors:  Carmelo Carmona-Rivera; Dimitre R Simeonov; Nicholas D Cardillo; William A Gahl; Carmen L Cadilla
Journal:  Biochim Biophys Acta       Date:  2012-10-23

4.  Genome-wide analysis of AP-3-dependent protein transport in yeast.

Authors:  Vikram C Anand; Lydia Daboussi; Todd C Lorenz; Gregory S Payne
Journal:  Mol Biol Cell       Date:  2008-12-30       Impact factor: 4.138

5.  Organelle biogenesis: en BLOC exchange for RAB32 and RAB38.

Authors:  Michael S Marks
Journal:  Curr Biol       Date:  2012-11-20       Impact factor: 10.834

6.  Caenorhabditis elegans HOPS and CCZ-1 mediate trafficking to lysosome-related organelles independently of RAB-7 and SAND-1.

Authors:  Jared L Delahaye; Olivia K Foster; Annalise Vine; Daniel S Saxton; Thomas P Curtin; Hannah Somhegyi; Rebecca Salesky; Greg J Hermann
Journal:  Mol Biol Cell       Date:  2014-02-05       Impact factor: 4.138

7.  Function and regulation of the Caenorhabditis elegans Rab32 family member GLO-1 in lysosome-related organelle biogenesis.

Authors:  Caitlin Morris; Olivia K Foster; Simran Handa; Kimberly Peloza; Laura Voss; Hannah Somhegyi; Youli Jian; My Van Vo; Marie Harp; Fiona M Rambo; Chonglin Yang; Greg J Hermann
Journal:  PLoS Genet       Date:  2018-11-12       Impact factor: 5.917

8.  BLOC-3 mutated in Hermansky-Pudlak syndrome is a Rab32/38 guanine nucleotide exchange factor.

Authors:  Andreas Gerondopoulos; Lars Langemeyer; Jin-Rui Liang; Andrea Linford; Francis A Barr
Journal:  Curr Biol       Date:  2012-10-18       Impact factor: 10.834

9.  Hexa-Longin domain scaffolds for inter-Rab signalling.

Authors:  Luis Sanchez-Pulido; Chris P Ponting
Journal:  Bioinformatics       Date:  2020-02-15       Impact factor: 6.937

  9 in total

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