ライフサイエンスコーパス: sulfite reductase

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1 ase), or by Escherichia coli cysJI (encoding sulfite reductase).

2 e and of dsrC, associated with dissimilatory sulfite reductase).

3 cation is unique and independent of CysI and sulfite reductase.

4 first report of a coenzyme F(420)-dependent sulfite reductase.

5 dehydrogenase, a methanogenesis enzyme, and sulfite reductase, a detoxification enzyme.

6 n suggest that DCP68 is the siroheme protein sulfite reductase, a ferredoxin-dependent enzyme that pa

7 The consequences of reduced sulfite reductase activity in particular are exacerbated

8 s to grow slowly on metabolites that require sulfite reductase activity.

9 ductase), as well as cytosolic Fe-S enzymes (sulfite reductase and isopropylmalate isomerase).

10 -terminal half a dissimilatory-type siroheme sulfite reductase, and Fsr catalyzes the corresponding p

11 oad similarity to the hemoprotein subunit of sulfite reductase but has many significant differences i

12 Sulfite reductase catalyzes the six-electron reduction o

13 flavin oxidoreductase component of the CysJI sulfite reductase complex (CysJ(8)I(4)), we show that th

14 mparative sequence analysis of dissimilatory sulfite reductase (DSR) genes from closely and distantly

15 lic processes, and profiles of dissimilatory sulfite reductase (dsr) transcripts are consistent with

16 CR targeting the 16S rRNA, dissimilatory (bi)sulfite reductase (dsrAB), and dissimilatory arsenate re

17 sion with sequence similarity to the nitrite/sulfite reductase family.

18 mmuno-colocalization with antibodies against sulfite reductase from Arabidopsis thaliana.

19 The initial rate parameters for the purified sulfite reductase from M. tuberculosis were determined u

20 el, highly active, coenzyme F(420)-dependent sulfite reductase (Fsr) with a cell extract specific act

21 t may interact with HdrABC and dissimilatory sulfite reductase gamma subunit (DsrC) to perform novel

22 hic patterns of the functional dissimilatory sulfite reductase gene (dsrA) and the 16S rRNA gene in s

23 ologue of the gamma subunit of dissimilatory sulfite reductase, has been determined by NMR spectrosco

24 he first system was the reduction of E. coli sulfite reductase hemoprotein (SiR-HP).

25 The active center of the Escherichia coli sulfite reductase hemoprotein (SiRHP) is exquisitely des

26 nd nitrite catalyzed by the Escherichia coli sulfite reductase hemoprotein (SiRHP), we have determine

27 s coding for DsrAB, the enzyme dissimilatory sulfite reductase, inevitably also contain the gene codi

28 Sulfite reductase is a second autoxidizable electron tra

29 e, the prosthetic group for both nitrite and sulfite reductases, is a methylated, iron-containing mod

30 Thus the autoxidation of sulfite reductase, like that of the respiratory chain, o

31 ce a sulfate transporter mutant strain and a sulfite reductase mutant strain are fully virulent.

32 ain late evolving archaea, and dissimilatory sulfite reductases of bacteria and archaea.

33 and gamma subunits of reverse dissimilatory sulfite reductase (rdsr).

34 Like their nitrite reductase counterparts, sulfite reductases require a siroheme cofactor for catal

35 ing the nitrite reductases and dissimilatory sulfite reductase, respectively.

36 Assimilatory NADPH-sulfite reductase (SiR) from Escherichia coli is a struc

37 Sulfite reductase (SiR) is an essential enzyme of the su

38 Plant sulfite reductase (SiR; Enzyme Commission 1.8.7.1) catal

39 Deletion of sulfite reductase (sirA, originally misannotated nirA) r

40 ences or could arise from alterations of the sulfite reductase structure that arise from the isolatio

41 dentification of virus-encoded dissimilatory sulfite reductase suggests SUP05 viruses reprogram their

42 the sulfite scavengers sulfite oxidase (SO), sulfite reductase, UDP-sulfoquinovose synthase, and beta

43 Previously described sulfite reductases use nicotinamides and cytochromes as

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