Heme-ligating histidines in flavocytochrome b(558): identification of specific histidines in gp91(phox). (Q43645354)

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8 November 2019

title

Heme-ligating histidines in flavocytochrome b(558): identification of specific histidines in gp91(phox) (English)

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8 November 2019

2

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8 November 2019

author name string

K J Biberstine-Kinkade

1

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8 November 2019

R I Epstein

3

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8 November 2019

B A LeRoy

4

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8 November 2019

W M Nauseef

5

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8 November 2019

M C Dinauer

6

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8 November 2019

language of work or name

English

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publication date

18 June 2001

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Journal of Biological Chemistry

8 November 2019

published in

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8 November 2019

volume

276

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8 November 2019

issue

33

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8 November 2019

page(s)

31105-31112

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Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

8 November 2019

cites work

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The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex

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The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245

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Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b

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Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

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Cytochrome b-245 of the neutrophil superoxide-generating system contains two nonidentical hemes. Potentiometric studies of a mutant form of gp91phox

21 January 2018

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Gp91(phox) is the heme binding subunit of the superoxide-generating NADPH oxidase

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Biosynthesis of the phagocyte NADPH oxidase cytochrome b558. Role of heme incorporation and heterodimer formation in maturation and stability of gp91phox and p22phox subunits

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Biosynthesis of flavocytochrome b558 . gp91(phox) is synthesized as a 65-kDa precursor (p65) in the endoplasmic reticulum.

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Gene therapy for chronic granulomatous disease

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Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA.

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Topological mapping of neutrophil cytochrome b epitopes with phage-display libraries

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Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox

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Neutrophils exposed to bacterial lipopolysaccharide upregulate NADPH oxidase assembly

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Phage display epitope mapping of human neutrophil flavocytochrome b558. Identification of two juxtaposed extracellular domains

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The cytosolic activating factors p47phox and p67phox have distinct roles in the regulation of electron flow in NADPH oxidase

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Subcellular localization of the b-cytochrome component of the human neutrophil microbicidal oxidase: translocation during activation

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Novel homologs of gp91phox.

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X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

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Hematologically important mutations: X-linked chronic granulomatous disease (second update).

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Analysis of glycosylation sites on gp91phox, the flavocytochrome of the NADPH oxidase, by site-directed mutagenesis and translation in vitro

21 January 2018

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Cytochrome b558: the flavin-binding component of the phagocyte NADPH oxidase.

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Epitope identification for human neutrophil flavocytochrome b monoclonals 48 and 449.

21 January 2018

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Antibody imprint of a membrane protein surface. Phagocyte flavocytochrome b

21 January 2018

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Design and synthesis of multi-haem proteins

21 January 2018

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Absence of both cytochrome b−245 subunits from neutrophils in X-linked chronic granulomatous disease

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M103327200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11413138%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

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