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10.1021/acs.chemrestox.9b00049

The rate constants for nucleophilic attack (Schiff base/iminium ion formation) by the lysine and methylated lysine analogues are indistinguishable.

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10.1039/c9ob01038f

Enzymatic and computational studies on the simplest lysine analogues that possess a modified main chain demonstrate that the lysine's backbone contributes significantly to functional KMT binding and catalysis.

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10.1021/acssynbio.8b00421

In this context, chemoselective reactive pyrrolysine analogues (CR-OAs) are of particular value, as this class of unnatural amino acids, among other useful properties, covers a wide range of different chemoselective reactions.

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10.1111/bjh.16077

Plasminogen contains 5 conserved kringle domains that bind to exposed lysine residues on fibrin (Abdul et al, 2016), which can be inhibited by the lysine analogues e-aminocaproic and TXA.

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Lysine Levels Lysine Ratio Lysine Deacetylase Lysine Acetyltransferase Lysine Succinylation Lysine Modification Lysine Oxidation Lysine 120 Lysine Requirement Lysine Specific Lysine Methylation Lysine Utilization Lysine Acylation Lysine 27 Lysine 2 Hydroxyisobutyrylation Lysine Crotonylation Lysine Demethylases Lysine Acetylome Lysine Residues Lysine Decarboxylase Lysine 9 Lysine Specific Histone Lysine 36 Lysine Acetylation Lysine Level Lysine Methyltransferases Lysine 16 Lysine Deacetylases Lysine Salt Lysine Acetyltransferases Lysine Selective Molecular Lysine Supplementation Lysine 107 Lysine Sulfate Lysine Residue Lysine Modified Lysine 63 Lysine Malonylation Lysine Methyltransferase Lysine Derivatives Lysine Crotonylome Lysine Requirements Lysine Biosynthesis Lysine 20 Lysine 4 Lysine Production Lysine B Hydroxybutyrylation Lysine Specific Demethylase Lysine Content Lysine Ratios Explore More

Keywords related to Analogues

Ii Analogues Heterocyclic Analogues Ice Analogues Product Analogues Protein Analogues Gnrh Analogues Modified Analogues Curcumin Analogues Related Analogues Structural Analogues Base Analogues Largazole Analogues Tissue Analogues Selenium Analogues Carboxamide Analogues Somatostatin Analogues Chalcone Analogues Resveratrol Analogues Nucleoside Analogues Neonicotinoid Analogues Blue Analogues Model Analogues C Analogues Proline Analogues Teixobactin Analogues Glp1 Analogues Tranylcypromine Analogues Porphyrin Analogues Nucleotide Analogues Molecule Analogues Pyrazole Analogues Dust Analogues Synthetic Analogues Molecular Analogues Tryptophan Analogues Cholesterol Analogues Substrate Analogues Insulin Analogues Terrestrial Analogues Milk Analogues Climate Analogues Semisynthetic Analogues Liquid Analogues Nucleostide Analogues Glp 1 Analogues Fentanyl Analogues Hormone Analogues Nucleoside Nucleotide Analogues Carbene Analogues Novel Analogues Explore More

Lysine Analogues

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Jan 16, 2025

What is/are Lysine Analogues?

Lysine Analogues - The rate constants for nucleophilic attack (Schiff base/iminium ion formation) by the lysine and methylated lysine analogues are indistinguishable. ^[1] Enzymatic and computational studies on the simplest lysine analogues that possess a modified main chain demonstrate that the lysine's backbone contributes significantly to functional KMT binding and catalysis. ^[2] In this context, chemoselective reactive pyrrolysine analogues (CR-OAs) are of particular value, as this class of unnatural amino acids, among other useful properties, covers a wide range of different chemoselective reactions. ^[3] Plasminogen contains 5 conserved kringle domains that bind to exposed lysine residues on fibrin (Abdul et al, 2016), which can be inhibited by the lysine analogues e-aminocaproic and TXA. ^[4]