Medical

mutase

Also found in: Dictionary, Encyclopedia, Wikipedia.

mutase

 [mu´tās]
any of a group of enzymes (transferases) that catalyze the intramolecular shifting of a chemical group from one position to another.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.

mu·tase

(myū'tās),
Any enzyme that catalyzes the apparent migration of groups within one molecule, for example, phosphoglycerate phosphomutase; sometimes the transfer is from one molecule to another, for example, phosphoglucomutase, phosphoglyceromutase (both phosphotransferases).
Farlex Partner Medical Dictionary © Farlex 2012

mutase

(myo͞o′tās, -tāz)
n.
An enzyme that catalyzes the shifting of a chemical group from one position to another within the same molecule.
The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.

mu·tase

(myū'tās)
Any enzyme that catalyzes the apparent migration of groups within one molecule; sometimes the transfer is from one molecule to another.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012
Mentioned in
References in periodicals archive
This organic acid buildup is caused by one of three mechanisms: genetic defect or absence of the enzyme methylmalonic acid coenzyme A mutase (mut), defect in the synthesis and transport of mut's cofactor 5'-deoxyadenosylcobalamin, and defect in the mitochondrial transport of cobalamin.
Moreover, the recent discovery of the whole synthesis pathway of Pyl, with PylB being a lysine mutase [13] shows that Pyl is entirely a derivative of a proteogenic amino acid (two lysines) and this could make sense in the light of the coevolution theory, such are the cases of Asp/Asn and Glu/Gln in Archaea[63].
Another enzyme, hydroxylaminobenzene mutase, catalyzes the conversion of hydroxylaminobenzene to 2-aminophenol through Bamberger rearrangement (Figure 2).
2011, details unpublished), phosphoglycerate kinase (PfPGK) [24], and phosphoglycerate mutase (PfPGM) [25] have been solved.
In mammalian cells, CNCbl and OHCbl are inactive forms and AdoCbl acts as a coenzyme of methylmalonyl Co-A mutase in mitochondria.
Molecular modeling, dynamics, and an insight into the structural inhibition of cofactor independent phosphoglycerate mutase isoform-1 from Wuchereria bancrofti using cheminformatics and mutational studies.
These genes include both the myosin heavy and light chain, and the phosphoglycerate mutase 2 (pgam2) gene.
MMA is a compound that can build up in the bloodstream if there isn't enough vitamin B12 in the body for an enzyme, methylmalonyl-CoA mutase, to function properly.
This vitamin exerts its physiological action through two enzymatic pathways: the first acts as a co-factor for the methionine synthase enzyme that converts homocysteine into methionine and the second acts upon L-methylmalonyl Coenzyme A (CoA) mutase enzyme to convert methylmalonyl-CoA into succinyl-CoA4.
Celano, "Evaluation of a Nested-PCR assay based on the phosphoglucosamine mutase gene (glmM) for the detection of Helicobacter pylori from raw milk" Food Control, vol.
The Helicobacter pylori ureC gene codes for a phosphoglucosamine mutase. J Bacteriol 1997; 179:3488-3493.
MMA can build up in the bloodstreamif there is not enough vitamin [B.sub.12] in the body for an enzyme (methylmalonyl-CoA mutase) to function properly.
Copyright © 2003-2025 Farlex, Inc Disclaimer
All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.