[The unique FauI restriction-modification system: cloning and comparative analysis of protein structure]
- PMID: 12942634
[The unique FauI restriction-modification system: cloning and comparative analysis of protein structure]
Abstract
The nucleotide sequence was established for the full-length Flavobacterium aquatile operon coding for the FauI restriction-modification system. The operon is unusual in structure and has the gene order control protein gene-DNA methyltransferase A gene-restriction endonuclease gene-DNA methyltransferase B gene, other than in the known analogs. The genes are similarly oriented and overlap. On evidence of sequence analysis, both methyltransferases are C5 enzymes, the control protein is similar to that of other restriction-modification systems, and restriction endonuclease is low-homologous to other enzymes cleaving the DNA upper strand in position 4 or 5 relative to the recognition site.
Similar articles
-
[Gene cloning, comparative analysis of the protein structures from Fsp4HI restriction-modification system and biochemical characterization of the recombinant DNA methyltransferase].Mol Biol (Mosk). 2007 Jan-Feb;41(1):43-50. Mol Biol (Mosk). 2007. PMID: 17380890 Russian.
-
[Cloning, primary structure determination and comparative analysis of DNA-methyltransferases from SfaNI and Bst19I restriction-modification systems].Mol Biol (Mosk). 2004 Nov-Dec;38(6):997-1004. Mol Biol (Mosk). 2004. PMID: 15612585 Russian.
-
Cloning and characterization of the gene encoding M.FauI DNA methyltransferase.Biol Chem. 1998 Apr-May;379(4-5):567-8. Biol Chem. 1998. PMID: 9628355
-
The organization and control of expression of the Pst I restriction-modification system.Gene Amplif Anal. 1987;5:209-26. Gene Amplif Anal. 1987. PMID: 3333366 Review. No abstract available.
-
The Pvu II restriction-modification system: cloning, characterization and use in revealing an E. coli barrier to certain methylases or methylated DNAs.Gene Amplif Anal. 1987;5:227-45. Gene Amplif Anal. 1987. PMID: 3333367 Review. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous