ライフサイエンスコーパス: cytochrome c6

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1 cted the interaction of the PSI complex with cytochrome c6.

2 , membrane-anchored cytochrome f and soluble cytochrome c6.

3 essed spontaneously owing to accumulation of cytochrome c6 (a functional substitute for plastocyanin)

4 fy sites of interaction between plastocyanin/cytochrome c6 and the PSI core, site-directed mutations

5 ame configuration relative to the heme as in cytochrome c6 and we propose that this stereochemistry d

6 ore structure to that of bacterial and algal cytochromes c6 but is unable to fulfill the same functio

7 mitochondrial cytochromes c, c1; chloroplast cytochromes c6, cf; bacterial cytochromes c2, c550, c551

8 In contrast, cytochrome c6 could not function as an electron donor to

9 6f complex (cyt b6f), plastocyanin (PC), and cytochrome c6 (cyt c6) from Chlamydomonas reinhardtii al

10 ally replaced by the heme-containing protein cytochrome c6 (cyt c6) in the green alga Chlamydomonas r

11 their redox partners, plastocyanin (PC) and cytochrome c6 (cyt c6) in the same species to study the

12 that complements both the cytochrome b6f and cytochrome c6 deficiencies in abf3.

13 potential is more than 200 mV below that of cytochrome c6 despite having His and Met as axial heme-i

14 The observed increased expression of cytochrome c6 during ripening suggests that it could act

15 anscript was expressed coordinately with the cytochrome c6-encoding (Cyc6) gene, which is known to be

16 he difference in potential, the structure of cytochrome c6 from the cyanobacterium Phormidium laminos

17 tid-encoded cytochrome f and nucleus-encoded cytochrome c6 have been identified and analyzed.

18 step in the evolution of cytochrome c6A from cytochrome c6, inhibiting reduction by the cytochrome b6

19 kets is that a highly conserved Gln (Q51) in cytochrome c6 is replaced by Val (V52) in c6A.

20 Electron transfer rates, measured by cytochrome c6-mediated NADP+ photoreduction, were lower

21 istent with the measurements of the rates of cytochrome c6-NADP+ reductase activity, indicating lower

22 ystem I (PSI) interacts with plastocyanin or cytochrome c6 on the luminal side.

23 iated electron transfer activity when either cytochrome c6 or an artificial electron donor was used.

24 brane electron transfer from plastocyanin or cytochrome c6 to the ferredoxin-NADP complex.

25 lakoid lumen suggest that it is derived from cytochrome c6, which functions in photosynthetic electro

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