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Literature DB >> 15342608

Processing of the tail lysozyme (gp5) of bacteriophage T4.

Abstract

The processing site of gp5 has been determined to be between residues Val-390 and His-391, instead of Ser-351 and Ala-352 as previously reported (H. Kanamaru, N. C. Gassner, N. Ye, S. Takeda, and F. Arisaka, J. Bacteriol. 181:2739-2744). Moreover, the maturation of gp5 is abolished by null mutations in other hub genes, indicating that cleavage requires the interactions of several baseplate proteins.

Entities: Chemical Mutation Species

Mesh：

Substances：

Year: 2004 PMID： 15342608 PMCID： PMC515172 DOI： 10.1128/JB.186.18.6335-6339.2004

Source DB: PubMed Journal: J Bacteriol ISSN： 0021-9193 Impact factor: 3.490

18 in total

1. The C-terminal fragment of the precursor tail lysozyme of bacteriophage T4 stays as a structural component of the baseplate after cleavage.

Authors: S Kanamaru; N C Gassner; N Ye; S Takeda; F Arisaka
Journal: J Bacteriol Date: 1999-05 Impact factor: 3.490

2. Isolation and characterization of the bacteriophage T4 tail-associated lysozyme.

Authors: H Nakagawa; F Arisaka; S Ishii
Journal: J Virol Date: 1985-05 Impact factor: 5.103

3. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors: H Towbin; T Staehelin; J Gordon
Journal: Proc Natl Acad Sci U S A Date: 1979-09 Impact factor: 11.205

4. Purification, characterization and reassembly of the bacteriophage T4D tail sheath protein P18.

Authors: J Tschopp; F Arisaka; R van Driel; J Engel
Journal: J Mol Biol Date: 1979-02-25 Impact factor: 5.469

5. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors: U K Laemmli
Journal: Nature Date: 1970-08-15 Impact factor: 49.962

6. Polyacrylamide gel electrophoresis in sodium dodecyl sulfate-containing buffers using multiphasic buffer systems: properties of the stack, valid Rf- measurement, and optimized procedure.

Authors: M Wyckoff; D Rodbard; A Chrambach
Journal: Anal Biochem Date: 1977-04 Impact factor: 3.365

7. [Carboxypeptidase Y as a biochemical reagent].

Authors: R Hayashi
Journal: Tanpakushitsu Kakusan Koso Date: 1983-12

8. Genetic control of bacteriophage T4 baseplate morphogenesis. III. Formation of the central plug and overall assembly pathway.

Authors: Y Kikuchi; J King
Journal: J Mol Biol Date: 1975-12-25 Impact factor: 5.469

Processing of the tail lysozyme (gp5) of bacteriophage T4.

1. The C-terminal fragment of the precursor tail lysozyme of bacteriophage T4 stays as a structural component of the baseplate after cleavage.

2. Isolation and characterization of the bacteriophage T4 tail-associated lysozyme.

3. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

4. Purification, characterization and reassembly of the bacteriophage T4D tail sheath protein P18.

5. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

6. Polyacrylamide gel electrophoresis in sodium dodecyl sulfate-containing buffers using multiphasic buffer systems: properties of the stack, valid Rf- measurement, and optimized procedure.

7. [Carboxypeptidase Y as a biochemical reagent].

8. Genetic control of bacteriophage T4 baseplate morphogenesis. III. Formation of the central plug and overall assembly pathway.

9. Identification of bacteriophage T4D gene products 26 and 51 as baseplate hub structural components.

10. A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.

1. Broad-host-range Yersinia phage PY100: genome sequence, proteome analysis of virions, and DNA packaging strategy.

2. Multifunctional roles of a bacteriophage phi 29 morphogenetic factor in assembly and infection.