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PMID: 10690633 Published · ppublish English Journal Article

Is the HemK family of putative S-adenosylmethionine-dependent methyltransferases a "missing" zeta subfamily of adenine methyltransferases? A hypothesis.

IUBMB life ·Vol. 48 ·No. 3 ·1999-09-00 ·Pages 247-9

Bujnicki JM, Radlinska M

Abstract

Previous comparative studies revealed close similarity among various groups of S-adenosyl-L-methionine (AdoMet)-dependent methyltransferases (MTases), indicating their common evolutionary origin. We present evidence for a remarkable similarity between the sequence and predicted structure of HemK (a widespread family of putative proteins encoded in genomes from bacteria to humans) and the catalytic domain of the gamma-subfamily of adenine-specific DNA MTases (N6mA MTases). We predict the structure and function of the putative catalytic domain of HemK proteins and speculate that the target-recognizing function may be conferred by the N-terminal variable region.

MeSH Terms
Amino Acid Sequence Animals Bacterial Proteins/genetics Escherichia coli Proteins Humans Methyltransferases/genetics Molecular Sequence Data Protein Methyltransferases Sequence Alignment Sequence Analysis Site-Specific DNA-Methyltransferase (Adenine-Specific)/classification,genetics
Chemicals
Bacterial Proteins Escherichia coli Proteins Methyltransferases Protein Methyltransferases S-adenosylmethionine-dependent phosphate methyltransferase prmC protein, E coli Site-Specific DNA-Methyltransferase (Adenine-Specific)
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bujnicki J M
Molecular Biology Research Program, Henry Ford Health System, Detroit, Michigan 48202, USA. [email protected]
Radlinska M
Article Info
Journal
IUBMB life
Abbr.
IUBMB Life
ISSN
1521-6543
Published
1999-09-00
Pages
247-9
Language
English
Region
England
NLM ID
100888706
Subset
IM
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