Mutagenesis of p22(phox) histidine 94. A histidine in this position is not required for flavocytochrome b558 function (Q24298671)

cytochrome b-245 beta chain

GOA release 2020-03-11

1 reference

protein heterodimerization activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Karla J Biberstine-Kinkade

1

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Lixin Yu

2

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Natalie Stull

3

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Brendan LeRoy

4

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Shelley Bennett

5

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Andrew Cross

6

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Mary C Dinauer

Journal of Biological Chemistry

7

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language of work or name

English

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publication date

16 August 2002

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published in

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volume

277

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issue

33

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page(s)

30368-74

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cites work

Cytochrome b-245 is a flavocytochrome containing FAD and the NADPH-binding site of the microbicidal oxidase of phagocytes

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Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000

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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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Novel homologs of gp91phox.

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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

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Identification of a spectrally stable proteolytic fragment of human neutrophil flavocytochrome b composed of the NH2-terminal regions of gp91(phox) and p22(phox).

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

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156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox

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Role of Src homology 3 domains in assembly and activation of the phagocyte NADPH oxidase

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Assembly of the phagocyte NADPH oxidase: binding of Src homology 3 domains to proline-rich targets

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

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Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).

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

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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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Creation of a genetic system for analysis of the phagocyte respiratory burst: high-level reconstitution of the NADPH oxidase in a nonhematopoietic system

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The association of FAD with the cytochrome b-245 of human neutrophils

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Prediction and comparison of the haem-binding sites in membrane haemoproteins

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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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Cloning and sequencing of the bovine flavocytochrome b subunit proteins, gp91-phox and p22-phox: comparison with other known flavocytochrome b sequences.

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Characterization of neutrophilb-type cytochrome in situ by electron paramagnetic resonance spectroscopy

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Generation of superoxide by purified and relipidated cytochrome b559 in the absence of cytosolic activators

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Characterization of the GTP-dependent activation of the superoxide-producing NADPH oxidase in a cell-free system of pig neutrophils

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Cytochrome b558, a component of the phagocyte NADPH oxidase, is a flavoprotein

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Processing and Maturation of Flavocytochromeb558Include Incorporation of Heme as a Prerequisite for Heterodimer Assembly

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7 January 2021