ライフサイエンスコーパス: SecA protein

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1 ation was obtained also for Escherichia coli SecA protein.

2 which led to the overproduction of wild-type SecA protein.

3 he translocation apparatus by binding to the SecA protein.

4 Y, SecE and SecG (SecYEG) and the peripheral SecA protein.

5 ked between amino acid residues 75 and 97 of SecA protein.

6 in in SecA2, unlike in SecA1 or conventional SecA proteins.

7 itates precursor targeting by binding to the SecA protein, a component of the membrane-embedded trans

8 was employed to generate defined peptides of SecA protein after photocross-linking with [alpha-(32)P]

9 location pathway that involves the essential SecA protein and the membrane-bound SecYEG translocon is

10 basal expression, reduced auto-repression by SecA protein, and abolished the responsiveness of secA e

11 e by overproduction of membrane-stuck mutant SecA proteins, and, in one case, a membrane-associated S

12 in translocation ATPase of Escherichia coli, SecA protein, auto-regulates its translation by binding

13 onstrate that the carboxyl-terminal third of SecA protein binds to the amino-terminal 107 amino acid

14 basal expression, reduced auto-repression by SecA protein, but retained a normal pattern of derepress

15 to the accessory Sec system is an accessory SecA protein called SecA2.

16 Bacterial SecA proteins can be categorized by the presence or abse

17 ong with collisional quenchers with a set of SecA proteins containing single tryptophan substitutions

18 sfer methodology with genetically engineered SecA proteins containing unique pairs of tryptophan and

19 sfer methodology with genetically engineered SecA proteins containing unique pairs of tryptophan and

20 mutational alteration, it is suggested that SecA protein contains two distinct RNA-binding sites.

21 ractionation studies which demonstrated that SecA proteins defective in this region were found almost

22 The enzymatic activities of two SecA proteins from the same microorganism have not been

23 teraction with SecA, no reciprocal study for SecA protein has been reported to date.

24 ues to determine the oligomeric structure of SecA protein in solution.

25 Increasing the level of SecA protein in the cell was found to reverse this slow-

26 rtance of the early amino-terminal region of SecA protein in the functioning of this domain, and demo

27 of this domain in regulating penetration of SecA protein into the inner membrane.

28 The SecA protein is present in all bacteria, and it is a cen

29 We produced a mutant SecA protein lacking residues 2-11, which was found to e

30 Furthermore, a hyperactive Azi-PrlD SecA protein of E. coli had increased PPXD and C-domain

31 eport the three-dimensional structure of the SecA protein of Mycobacterium tuberculosis.

32 The identification of an additional SecA protein, particularly in Gram-positive pathogens, h

33 translocons are saturated with ribosomes and SecA protein, reflecting the inherent affinity of these

34 acterium tuberculosis is the presence of two SecA proteins: SecA1, the essential "housekeeping" SecA,

35 Biochemical characterization of the mutant SecA proteins showed that Ser226, Val310, Ile789, Glu806

36 Azi- and PrlD-SecA proteins that confer azide-resistant and signal seq

37 SecA protein, the ATPase promoting translocation of prot

38 t of a small group of bacteria that have two SecA proteins: the canonical SecA (SecA1) and a second,

39 Binding of SecA protein to geneX-secA RNA or various mutant derivat

40 rystal structure of the Thermus thermophilus SecA protein (TtSecA).

41 The level of Azi- and PrlD-SecA protein was also elevated in inverted membrane vesi

42 teria, SecA1 is the essential 'housekeeping' SecA protein whereas SecA2 is an accessory secretion fac

43 ively in their integral membrane form, while SecA proteins with defects in the low-affinity ATP-domai

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