Literature DB >> 21045313

Crystallization and X-ray diffraction studies of DNA-free and DNA-bound forms of EcoO109I DNA methyltransferase.

Makoto Iwamoto1, Asami Hishiki, Takashi Shimada, Tsuyoshi Imasaki, Junko Tsuda, Keiko Kita, Toshiyuki Shimizu, Mamoru Sato, Hiroshi Hashimoto.   

Abstract

EcoO109I DNA methyltransferase (M.EcoO109I) is a type II modification enzyme from the EcoO109I restriction-modification system identified in Escherichia coli strain H709c. M.EcoO109I recognizes double-stranded RGGNCCY (where R = A or G, Y = T or C and N is any base) and transfers a methyl group to the C5 of the inner cytosines from S-adenosylmethionine. To reveal the mechanism of substrate recognition by M.EcoO109I, DNA-free and DNA-bound forms of M.EcoO109I were successfully crystallized. Crystals of the DNA-free and DNA-bound forms belonged to space groups P4(2)2(1)2, with unit-cell parameters a = b = 120.5, c = 79.8 Å, and P2(1), with unit-cell parameters a = 55.8, b = 77.4, c = 117.4 Å, β = 93.5°, respectively.

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Year:  2010        PMID: 21045313      PMCID: PMC3001666          DOI: 10.1107/S174430911003753X

Source DB:  PubMed          Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun        ISSN: 1744-3091


  9 in total

1.  Evidence of horizontal transfer of the EcoO109I restriction-modification gene to Escherichia coli chromosomal DNA.

Authors:  K Kita; J Tsuda; T Kato; K Okamoto; H Yanase; M Tanaka
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

2.  Structure of the N6-adenine DNA methyltransferase M.TaqI in complex with DNA and a cofactor analog.

Authors:  K Goedecke; M Pignot; R S Goody; A J Scheidig; E Weinhold
Journal:  Nat Struct Biol       Date:  2001-02

3.  Characterization and overproduction of EcoO109I methyltransferase.

Authors:  K Kita; J Tsuda; R Nishigaki
Journal:  Biosci Biotechnol Biochem       Date:  2001-11       Impact factor: 2.043

4.  A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes.

Authors:  Richard J Roberts; Marlene Belfort; Timothy Bestor; Ashok S Bhagwat; Thomas A Bickle; Jurate Bitinaite; Robert M Blumenthal; Sergey Kh Degtyarev; David T F Dryden; Kevin Dybvig; Keith Firman; Elizaveta S Gromova; Richard I Gumport; Stephen E Halford; Stanley Hattman; Joseph Heitman; David P Hornby; Arvydas Janulaitis; Albert Jeltsch; Jytte Josephsen; Antal Kiss; Todd R Klaenhammer; Ichizo Kobayashi; Huimin Kong; Detlev H Krüger; Sanford Lacks; Martin G Marinus; Michiko Miyahara; Richard D Morgan; Noreen E Murray; Valakunja Nagaraja; Andrzej Piekarowicz; Alfred Pingoud; Elisabeth Raleigh; Desirazu N Rao; Norbert Reich; Vladimir E Repin; Eric U Selker; Pang-Chui Shaw; Daniel C Stein; Barry L Stoddard; Waclaw Szybalski; Thomas A Trautner; James L Van Etten; Jorge M B Vitor; Geoffrey G Wilson; Shuang-yong Xu
Journal:  Nucleic Acids Res       Date:  2003-04-01       Impact factor: 16.971

5.  Crystal structures of type II restriction endonuclease EcoO109I and its complex with cognate DNA.

Authors:  Hiroshi Hashimoto; Toshiyuki Shimizu; Tsuyoshi Imasaki; Matsuri Kato; Naoki Shichijo; Keiko Kita; Mamoru Sato
Journal:  J Biol Chem       Date:  2004-12-07       Impact factor: 5.157

6.  Solvent content of protein crystals.

Authors:  B W Matthews
Journal:  J Mol Biol       Date:  1968-04-28       Impact factor: 5.469

7.  The crystal structure of HaeIII methyltransferase convalently complexed to DNA: an extrahelical cytosine and rearranged base pairing.

Authors:  K M Reinisch; L Chen; G L Verdine; W N Lipscomb
Journal:  Cell       Date:  1995-07-14       Impact factor: 41.582

8.  HhaI methyltransferase flips its target base out of the DNA helix.

Authors:  S Klimasauskas; S Kumar; R J Roberts; X Cheng
Journal:  Cell       Date:  1994-01-28       Impact factor: 41.582

9.  Structure and substrate recognition of the Escherichia coli DNA adenine methyltransferase.

Authors:  John R Horton; Kirsten Liebert; Miklos Bekes; Albert Jeltsch; Xiaodong Cheng
Journal:  J Mol Biol       Date:  2006-02-28       Impact factor: 5.469

  9 in total

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