Target type: biologicalprocess
The methylation of the N-terminal alanine of proteins. [RESID:AA0061, RESID:AA0062]
N-terminal peptidyl-alanine methylation is a post-translational modification that occurs on the N-terminal alanine residue of proteins. This process involves the transfer of a methyl group from a methyl donor, typically S-adenosyl methionine (SAM), to the α-amino group of the alanine residue. The reaction is catalyzed by a specific type of methyltransferase called N-terminal alanine methyltransferase.
The biological significance of N-terminal alanine methylation is not fully understood, but it is thought to play a role in a variety of cellular processes, including protein stability, protein folding, and protein-protein interactions. For example, N-terminal alanine methylation can affect the stability of proteins by protecting the N-terminus from proteolytic degradation. It can also influence the folding of proteins by affecting the interactions between the N-terminus and other regions of the protein. Additionally, N-terminal alanine methylation can alter the ability of proteins to interact with other molecules, which can have downstream effects on cellular signaling and other biological processes.
The specific function of N-terminal alanine methylation is likely to vary depending on the protein and the cellular context. Further research is needed to fully elucidate the biological roles of this post-translational modification.'
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Protein | Definition | Taxonomy |
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N-terminal Xaa-Pro-Lys N-methyltransferase 1 | A methyltransferase-like protein 11A that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9BV86] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
sch-202676 | SCH-202676: An allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors; structure in first source |