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InterPro: IPR002294 N6 adenine-specific DNA methyltransferase, D12 class
Protein matches
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UniProtKB Matches: 1171 proteins |
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Accession
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IPR002294 D12N6_MeTrfase |
Type
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Family |
Signatures
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InterPro Relationships
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Children
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IPR012186 Adenine modification methylase, M.StsI
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GO Term annotation
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Process
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GO:0006306 DNA methylation
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Function
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GO:0003677 DNA binding
GO:0009007 site-specific DNA-methyltransferase (adenine-specific) activity
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InterPro annotation
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Entry Details in BioMart
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Abstract
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In prokaryotes, the major role of DNA methylation is to protect host DNA against degradation by restriction enzymes. There are 2 major classes of DNA methyltransferase that differ in the nature of the modifications they effect. The members of one class (C-MTases) methylate a ring carbon and form C5-methylcytosine (see IPR001525). Members of the second class (N-MTases) methylate exocyclic nitrogens and form either N4-methylcytosine (N4-MTases) or N6-methyladenine (N6-MTases). Both classes of MTase utilise the cofactor S-adenosyl-L-methionine (SAM) as the methyl donor and are active as monomeric enzymes [1].
N-6 adenine-specific DNA methylases (EC:2.1.1.72) (A-Mtase) are enzymes that specifically methylate the amino group at the C-6 position of adenines in DNA. Such enzymes are found in the three existing types of bacterial restriction-modification systems (in type I system the A-Mtase is the product of the hsdM gene, and in type III it is the product of the mod gene). All of these enzymes recognise a specific sequence in DNA and methylate an adenine in that sequence. It has been shown [2, 3, 4, 5] that A-Mtases contain a conserved motif Asp/Asn-Pro-Pro-Tyr/Phe in their N-terminal section, this conserved region could be
involved in substrate binding or in the catalytic activity. The structure of N6-MTase TaqI (M.TaqI) has been resolved to 2.4 A [6]. The molecule folds into
2 domains, an N-terminal catalytic domain, which contains the catalytic and cofactor binding sites, and comprises a central 9-stranded beta-sheet, surrounded by 5 helices; and a C-terminal DNA recognition domain, which is formed by 4 small beta-sheets and 8 alpha-helices. The N- and C-terminal domains form a cleft that accommodates the DNA substrate. A classification of N-MTases has been proposed, based on conserved motif (CM) arrangements [5]. According to this classification, N6-MTases that
have a DPPY motif (CM II) occuring after the FxGxG motif (CM I) are
designated D12 class N6-adenine MTases.
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Structural links
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Database links
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Publications
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1.
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Cheng X.
Structure and function of DNA methyltransferases.
24 293-318 1995
[PubMed: 7663118]
http://dx.doi.org/10.1146/annurev.bb.24.060195.001453
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2.
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Loenen WA, Daniel AS, Braymer HD, Murray NE.
Organization and sequence of the hsd genes of Escherichia coli K-12.
J. Mol. Biol. 198 159-70 1987
[PubMed: 3323532]
http://dx.doi.org/10.1016/0022-2836(87)90303-2
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3.
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Narva KE, Van Etten JL, Slatko BE, Benner JS.
The amino acid sequence of the eukaryotic DNA [N6-adenine]methyltransferase, M.CviBIII, has regions of similarity with the prokaryotic isoschizomer M.TaqI and other DNA [N6-adenine] methyltransferases.
Gene 74 253-9 1988
[PubMed: 3248728]
http://dx.doi.org/10.1016/0378-1119(88)90298-3
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4.
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Lauster R.
Evolution of type II DNA methyltransferases. A gene duplication model.
J. Mol. Biol. 206 313-21 1989
[PubMed: 2541254]
http://dx.doi.org/10.1016/0022-2836(89)90481-6
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5.
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Timinskas A, Butkus V, Janulaitis A.
Sequence motifs characteristic for DNA [cytosine-N4] and DNA [adenine-N6] methyltransferases. Classification of all DNA methyltransferases.
Gene 157 3-11 1995
[PubMed: 7607512]
http://dx.doi.org/10.1016/0378-1119(94)00783-O
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6.
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Labahn J, Granzin J, Schluckebier G, Robinson DP, Jack WE, Schildkraut I, Saenger W.
Three-dimensional structure of the adenine-specific DNA methyltransferase M.Taq I in complex with the cofactor S-adenosylmethionine.
Proc. Natl. Acad. Sci. U.S.A. 91 10957-61 1994
[PubMed: 7971991]
http://www.pubmedcentral.nih.gov/picrender.fcgi?tool=EBI&pubmedid=7971991&action=stream&blobtype=pdf
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Additional Reading
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Willcock DF, Dryden DT, Murray NE.
A mutational analysis of the two motifs common to adenine methyltransferases.
EMBO J. 13 1994 3902-8
[PubMed: 8070417]
http://www.pubmedcentral.nih.gov/picrender.fcgi?tool=EBI&pubmedid=8070417&action=stream&blobtype=pdf
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Horton JR, Liebert K, Hattman S, Jeltsch A, Cheng X.
Transition from nonspecific to specific DNA interactions along the substrate-recognition pathway of dam methyltransferase.
Cell 121 2005 349-61
[PubMed: 15882618]
http://dx.doi.org/10.1016/j.cell.2005.02.021
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Tran PH, Korszun ZR, Cerritelli S, Springhorn SS, Lacks SA.
Crystal structure of the DpnM DNA adenine methyltransferase from the DpnII restriction system of streptococcus pneumoniae bound to S-adenosylmethionine.
Structure 6 1998 1563-75
[PubMed: 9862809]
http://dx.doi.org/10.1016/S0969-2126(98)00154-3
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Yang Z, Horton JR, Zhou L, Zhang XJ, Dong A, Zhang X, Schlagman SL, Kossykh V, Hattman S, Cheng X.
Structure of the bacteriophage T4 DNA adenine methyltransferase.
Nat. Struct. Biol. 10 2003 849-55
[PubMed: 12937411]
http://dx.doi.org/10.1038/nsb973
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InterPro 23.1
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