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InterPro: IPR002295 N6 adenine-specific DNA methyltransferase, D21 class

Protein matchesHelp
UniProtKB
Matches:
634 proteins
AccessionHelp IPR002295 D21N6_MeTrfase
TypeHelp Domain
SignaturesHelp
InterPro RelationshipsHelp
Contains IPR002052 DNA methylase, N-6 adenine-specific, conserved site
GO Term annotationHelp
Process GO:0006306 DNA methylation
Function GO:0003677 DNA binding
GO:0008170 N-methyltransferase activity
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

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 before the FxGxG motif (CM I) are designated D21 class N6-adenine MTases.

Structural linksHelp
SCOP: c.66.1.11
CATH: 3.40.50.150
Database linksHelp
Enzyme: EC:2.1.1
Blocks: IPB002295

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR002295 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
P08763 Type III restriction-modification system EcoPI enzyme mod

P14751 Modification methylase RsrI

Q9Y5R4 HemK methyltransferase family member 1

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR002941 DNA methylase N-4/N-6
IPR007848 Methyltransferase small
IPR004556 Modification methylase HemK
IPR002295 N6 adenine-specific DNA methyltransferase, D21 class
IPR002052 DNA methylase, N-6 adenine-specific, conserved site
SWISS-MODEL
PDB Chain
ModBase
CATH Domain
SCOP Domain

PublicationsHelp
1. 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
2. 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
3. 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
4. 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
5. 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
6. 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

Additional ReadingHelp
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
Thomas CB, Scavetta RD, Gumport RI, Churchill ME.
Structures of liganded and unliganded RsrI N6-adenine DNA methyltransferase: a distinct orientation for active cofactor binding.
J. Biol. Chem. 278 2003 26094-101 [PubMed: 12732637]
http://dx.doi.org/10.1074/jbc.M303751200
Scavetta RD, Thomas CB, Walsh MA, Szegedi S, Joachimiak A, Gumport RI, Churchill ME.
Structure of RsrI methyltransferase, a member of the N6-adenine beta class of DNA methyltransferases.
Nucleic Acids Res. 28 2000 3950-61 [PubMed: 11024175]
http://dx.doi.org/10.1093/nar/28.20.3950
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InterPro 23.1