ライフサイエンスコーパス: cytochrome b558

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1 lieved to be located on the beta, subunit of cytochrome b558.

2 ion of quinol is by the low-spin ferri-haem, cytochrome b558.

3 e associated with the same membrane protein, cytochrome b558.

4 e that allows p67PHOX to interact fully with cytochrome b558.

5 hed a direct interaction between p67PHOX and cytochrome b558.

6 OX, p40PHOX, and Rac with the membrane-bound cytochrome b558.

7 l domain of p67PHOX increased its binding to cytochrome b558.

8 The phagocyte cytochrome b558, a heterodimer comprised of gp91phox and

9 e plasma membrane, where they associate with cytochrome b558, a membrane-bound flavohemoprotein, to a

10 We have recently cloned the cytochrome b558 alpha-subunit, p22(phox) (one of the key

11 rates to the plasma membrane to complex with cytochrome b558, an oxidase-specific flavohemoprotein.

12 dase, Rap1A/Krev1 because it copurifies with cytochrome b558 and p190Ras-GAP because it inhibits the

13 comprising a membrane-bound flavocytochrome (cytochrome b558) and at least four cytosolic components:

14 eme incorporation plays an important role in cytochrome b558 assembly and provide further support for

15 chrome c reductase-containing fraction and a cytochrome b558-associated fraction.

16 The role of heme in cytochrome b558 biosynthesis was studied using succinyl

17 ears to increase the binding of p67(PHOX) to cytochrome b558 by serving as an adapter, bringing p67PH

18 il oxidative killing by preventing fusion of cytochrome b558-carrying specific granules and secretory

19 Upon incorporation into liposomes, the cytochrome b558-containing fraction demonstrates high O2

20 ng site through which p47phox interacts with cytochrome b558 during the activation process.

21 The reduction in cytochrome b558 expression and NADPH oxidase activity wa

22 The cytochrome b558 heavy chain (gp9l-phox) is expressed in

23 e murine gp91phox subunit forms a functional cytochrome b558 heterodimer with human oxidase subunits,

24 SF may have resulted in increased content of cytochrome b558 in the cell membrane, it did not alter t

25 erns for O2- generation and INT reduction by cytochrome b558 incorporated into artificial liposomes s

26 The NADPH oxidase cytochrome b558 is a membrane heterodimer comprised of a

27 Cytochrome b558 is the essential component of the NADPH

28 nic granulomatous disease patients that lack cytochrome b558 or p47phox and have a defective NADPH ox

29 hibits interaction with the small subunit of cytochrome b558, p22phox.

30 phosphorylated p40PHOX alone did not bind to cytochrome b558, phosphorylated p47PHOX did, and, moreov

31 plement C1q, lysozyme M, cathepsins S and Z, cytochrome b558 small subunit, macrophage-specific prote

32 Interestingly, CL097 induced cytochrome b558 translocation to the plasma membrane and

33 e activity, found in microsomes containing a cytochrome b558, was a major source of O2.- production i

34 dapter, bringing p67PHOX into proximity with cytochrome b558, whereas phosphorylated p40(PHOX) may in

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