Literature DB >> 1692159

Cloning of a 67-kD neutrophil oxidase factor with similarity to a noncatalytic region of p60c-src.

T L Leto1, K J Lomax, B D Volpp, H Nunoi, J M Sechler, W M Nauseef, R A Clark, J I Gallin, H L Malech.   

Abstract

Chronic granulomatous diseases (CGDs) are characterized by recurrent infections resulting from impaired superoxide production by a phagocytic cell, nicotinamide adenine dinucleotide phosphate (reduced) (NADPH) oxidase. Complementary DNAs were cloned that encode the 67-kilodalton (kD) cytosolic oxidase factor (p67), which is deficient in 5% of CGD patients. Recombinant p67 (r-p67) partially restored NADPH oxidase activity to p67-deficient neutrophil cytosol from these patients. The p67 cDNA encodes a 526-amino acid protein with acidic middle and carboxyl-terminal domains that are similar to a sequence motif found in the noncatalytic domain of src-related tyrosine kinases. This motif was recently noted in phospholipase C-gamma, nonerythroid alpha-spectrin (fodrin), p21ras-guanosine triphophatase-activating protein (GAP), myosin-1 isoforms, yeast proteins cdc-25 and fus-1, and the 47-kD phagocyte oxidase factor (p47), which suggests the possibility of common regulatory features.

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Year:  1990        PMID: 1692159     DOI: 10.1126/science.1692159

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  82 in total

1.  The PB1 domain and the PC motif-containing region are structurally similar protein binding modules.

Authors:  Sosuke Yoshinaga; Motoyuki Kohjima; Kenji Ogura; Masashi Yokochi; Ryu Takeya; Takashi Ito; Hideki Sumimoto; Fuyuhiko Inagaki
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

Review 2.  Assembly of the phagocyte NADPH oxidase.

Authors:  William M Nauseef
Journal:  Histochem Cell Biol       Date:  2004-08-04       Impact factor: 4.304

Review 3.  The molecular pathology of primary immunodeficiencies.

Authors:  Megan S Lim; Kojo S J Elenitoba-Johnson
Journal:  J Mol Diagn       Date:  2004-05       Impact factor: 5.568

4.  Towards routine screening of rare genetic diseases: the example of chronic granulomatous disease.

Authors:  Marie José Stasia
Journal:  J Mol Diagn       Date:  2010-03-19       Impact factor: 5.568

5.  A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.

Authors:  A Görlach; P L Lee; J Roesler; P J Hopkins; B Christensen; E D Green; S J Chanock; J T Curnutte
Journal:  J Clin Invest       Date:  1997-10-15       Impact factor: 14.808

6.  Novel domains in NADPH oxidase subunits, sorting nexins, and PtdIns 3-kinases: binding partners of SH3 domains?

Authors:  C P Ponting
Journal:  Protein Sci       Date:  1996-11       Impact factor: 6.725

7.  Involvement of GTP in cell-free activation of neutrophil NADPH oxidase. Studies with GTP analogues.

Authors:  E Klinger; I Aviram
Journal:  Biochem J       Date:  1992-07-15       Impact factor: 3.857

8.  Activation state-dependent interaction between Galphai and p67phox.

Authors:  Caroline Marty; Tohru Kozasa; Mark T Quinn; Richard D Ye
Journal:  Mol Cell Biol       Date:  2006-07       Impact factor: 4.272

Review 9.  Mechanisms for the activation/electron transfer of neutrophil NADPH-oxidase complex and molecular pathology of chronic granulomatous disease.

Authors:  S Umeki
Journal:  Ann Hematol       Date:  1994-06       Impact factor: 3.673

10.  Nox activator 1: a potential target for modulation of vascular reactive oxygen species in atherosclerotic arteries.

Authors:  Xi-Lin Niu; Nageswara R Madamanchi; Aleksandr E Vendrov; Igor Tchivilev; Mauricio Rojas; Chaitanya Madamanchi; Ralph P Brandes; Karl-Heinz Krause; Julia Humphries; Alberto Smith; Kevin G Burnand; Marschall S Runge
Journal:  Circulation       Date:  2010-01-18       Impact factor: 29.690

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