Page last updated: 2024-09-26

epsilon-n-methyllysine

Description

epsilon-N-methyllysine: RN given refers to (L-Lys)-isomer; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

N(6)-methyllysine : A lysine derivative that is lysine in which one of the hydrogens attached to N(6) is substituted by a methyl group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

N(6)-methyl-L-lysine : An L-lysine derivative that is L-lysine in which one of the hydrogens attached to N(6) is substituted by a methyl group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID164795
CHEBI ID17604
SCHEMBL ID64149
MeSH IDM0046580

Synonyms (36)

Synonym
(s)-2-amino-6-methylaminohexanoic acid
epsilon-n-methyllysine
n(epsilon)-methyl-l-lysine
CHEBI:17604
n-methyl-l-lysine
epsilon-methyllysine
1188-07-4
n(6)-methyllysine
n(zeta)-methyllysine
n-epsilon-methyllysine
n(6)-methyl-l-lysine
melys
(2s)-2-amino-6-(methylamino)hexanoic acid
n-methyl-lysine
mlz ,
n6-methyl-l-lysine ,
C02728
DB01714
1P0Y
unii-fcr6t2iyvu
l-lysine, n6-methyl-
fcr6t2iyvu ,
SCHEMBL64149
PQNASZJZHFPQLE-LURJTMIESA-N
DTXSID70152242
n6-methyllysine
.epsilon.-methyl-l-lysine
.epsilon.-n-methyl-l-lysine
.epsilon.-methyllysine
(2s)-2-amino-6-(methylamino)hexanoate
(s)-2-amino-6-methylaminohexanoate
n-epsilon-methyl-l-lysine
n~6~-methyl-l-lysine
Q3334174
n6-methyl-lysine; lc-tdda; ce10
(2s)-2-amino-6-methylamino-hexanoic acid

Drug Classes (2)

ClassDescription
L-lysine derivativeA proteinogenic amino acid derivative resulting from reaction of L-lysine at the amino group or the carboxy group, or from the replacement of any hydrogen of L-lysine by a heteroatom.
non-proteinogenic L-alpha-amino acidAny L-alpha-amino acid which is not a member of the group of 23 proteinogenic amino acids.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplastPisum sativum (garden pea)Ki100,800.000036,600.000068,700.0000100,800.0000AID977610
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplastPisum sativum (garden pea)Ki100,800.000036,600.000068,700.0000100,800.0000AID977610
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID977610Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB2003Nature structural biology, Jul, Volume: 10, Issue:7
Mechanism of multiple lysine methylation by the SET domain enzyme Rubisco LSMT.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (27)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (37.04)18.7374
1990's5 (18.52)18.2507
2000's8 (29.63)29.6817
2010's4 (14.81)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other27 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Bioavailability (1)

ArticleYear
Bioavailability of some lysine derivatives in mice.
The Journal of nutrition, Volume: 111, Issue: 8
1981
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]