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Pathway Description
1-Methylhistidine Metabolism
Homo sapiens
Metabolic Pathway
Created: 2021-08-23
Last Updated: 2023-06-27
Methylhistidine is a modified amino acid that is produced in myocytes during the methylation of actin and myosin. It is also formed from the methylation of L-histidine, which takes the methyl group from S-adenosylmethionine and forms S-adenosylhomocysteine as a byproduct. After its formation in the myocytes, methylhistidine enters the blood stream and travels to the kidneys, where it is excreted in the urine. Methylhistidine is present in the blood and urine in higher concentrations after skeletal muscle protein breakdown, which can occur due to disease or injury. Because of this, it can be used to judge how much muscle breakdown is occurring. Methylhistidine levels are also affected by diet, and may differ between vegetarian diets and those containing meats.
References
1-Methylhistidine Metabolism References
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Pubmed: 21945731
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Pubmed: 1143090
Huszar G, Elzinga M: Amino acid sequence around the single 3-methylhistidine residue in rabbit skeletal muscle myosin. Biochemistry. 1971 Jan 19;10(2):229-36. doi: 10.1021/bi00778a006.
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Pubmed: 15489334
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