ライフサイエンスコーパス: phage P22

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1 minase:L-terminase complex of the Salmonella phage P22.

2 biologically unrelated lysogenic salmonella phage P22.

3 ic domain.Virions of HK620 resemble those of phage P22.

4 coli phage lambda and Salmonella typhimurium phage P22.

5 sequences, and is required for the growth of phage P22.

6 iments with both coliphage P1 and Salmonella phage P22.

7 ted tailspike endorhamnosidase of Salmonella phage P22.

8 i phage lambda and of Salmonella typhimurium phage P22.

9 lements and a podophage distantly related to phage P22.

10 roduction of polyheads, never seen before in phage P22.

11 In phage P22, a member of the Podoviridae family that infec

12 rent Arm/BOX-B sequences in lambda's cousin, phage P22, account for some of the type specificity that

13 m ssrA mutants fail to support the growth of phage P22 and are delayed in their ability to form viabl

14 cted product of the uoi gene with Salmonella phage P22 and Streptomyces plasmid Xis proteins shows th

15 tructure comparison of distant homologs from phages P22 and lambda.

16 ar to those of the tailspikes of the related phages P22 and Sf6.

17 during infection with scaffolding deficient phage P22, and the products of assembly were analyzed.

18 site for the Mnt protein, a repressor of the phage P22 ant gene.

19 The Mnt protein of Salmonella phage P22 binds site-specifically to its operator.

20 This knob, absent in phage P22 but shared in other members of the P22-like ge

21 ailspike protein from Salmonella typhimurium phage P22 can be trapped in the cold.

22 Some amino acid substitutions in phage P22 coat protein cause a temperature-sensitive fol

23 Eighteen single amino acid substitutions in phage P22 coat protein cause temperature-sensitive foldi

24 Cold-sensitive mutations in phage P22 coat protein cause the accumulation of precurs

25 Three cold-sensitive mutants in phage P22 coat protein have been characterized to determ

26 The I-domain is a genetic insertion in the phage P22 coat protein that chaperones its folding and s

27 In the in vivo folding of phage P22 coat protein, amino acid substitutions that ca

28 Amino acid substitutions in phage P22 coat protein, known as tsf (temperature-sensit

29 ings suggest that the needle plays a role in phage P22 DNA delivery by controlling the kinetics of DN

30 logy for a family of proteins, including the phage P22 erf, the bacterial RecT, and the eukaryotic Ra

31 investigating the assembly of the Salmonella phage P22 has been exploited to elucidate the structural

32 Productive growth of phage P22 in wild-type Salmonella typhimurium correlates

33 rium MGS-7 via phage P1 and subsequently via phage P22 into the virulent Salmonella strain SL1344.

34 The portal vertex structure of the phage P22 is a 2.8 MDa molecular machine that mediates a

35 ble phage particles following induction of a phage P22 lysogen.

36 e course of a lytic infection the Salmonella phage P22 occasionally encapsulates bacterial DNA instea

37 Phage P22 procapsids are the product of the co-assembly

38 e have investigated the in vitro assembly of phage P22 procapsids using a quantitative model specific

39 Phage P22 scaffolding subunits are elongated 33-kDa mole

40 gation reaction have been identified for the phage P22 tailspike and coat proteins.

41 s been raised against Salmonella typhimurium phage P22 tailspike.

42 Mnt is a repressor from phage P22 that belongs to the ribbon-helix-helix family

43 that expression of the gtr genes encoded by phage P22 that confers the O1 serotype is under the cont

44 In phage P22, the tail contains a thin needle, encoded by t

45 The attachment of phage P22 to the host cell as well as the injection of t

46 Salmonella phage P22, which serves as an assembly paradigm for icos

47 ical to those of the short-tailed Salmonella phage P22, while other early genes are nearly identical

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