Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Muscle phosphoglycerate kinase

K.R. Fritz, P.J. Rat skeletal muscle phosphoglycerate kinase purification, characterization and comparison with the enzyme from rabbit skeletal muscle and brewer s yeast. Comp. Biochem. Physiol. B, 47, 879-893 (1974)... [Pg.308]

Kovari, Z. Flachner, B. Naray-Szabo, G. Vas, M. Crystallographic and thiol-reactivity studies on the complex of pig muscle phosphoglycerate kinase with ATP analogues correlation between nucleotide binding mode and helix flexibility. Biochemistry, 41, 8796-8806 (2002)... [Pg.312]

T25. Tsujino, S., Shanske, S., and DiMauro, S., Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency. Muscle Nerve (Suppl. 3), S45-S49 (1995). [Pg.52]

Scopes, R.K. 3-phosphoglycerate kinase of skeletal muscle. Methods EnzymoL, 42C, 127-134 (1975)... [Pg.309]

Stewart, A.A. Scopes, R.K. Phosphoglycerate kinase B from ram testis. Purification, characterisation and comparison with the muscle isoenzyme. Eur. J. Biochem., 85, 89-95 (1978)... [Pg.310]

Phosphoglycerate kinase deficiency, the seventh enzyme step of the glycolytic pathway, is an inherited X-linked recessive disorder, meaning it mostly affects males, although females are carriers. Onset is infancy to early adulthood. Symptoms may include anaemia, enlargement of the spleen, mental retardation and epilepsy (seizures) more rarely, weakness, exercise intolerance, muscle cramps and episodes of myoglobinuria occur. [Pg.271]

The fate of dihydroxyacetone phosphate is also varied—it may be transformed to a-glycerophosphate, or through the reaction catalyzed by the triose isomerase, it may yield D-glyceraldehyde-3-phosphate, which in the presence of triose phosphate dehydrogenase and phosphoglycerate kinase yields 3-phosphoglycerate. This degradation pathway is complete only in liver, and it is not known to what extent it operates in muscle. [Pg.16]

A different problem results from deficiency of enzymes of glycolysis such as phosphofructokinase (see Box 20-D), phosphoglycerate rnutase, and pyruvate kinase. Lack of one isoenzyme of phosphoglycerate rnutase in muscle leads to intolerance to strenuous exercise/ A deficiency in pyruvate kinase is one of the most common defects of glycolysis in erythrocytes and leads to a shortened erythrocyte lifetime and hereditary hemolytic anemia.s... [Pg.1002]

See other pages where Muscle phosphoglycerate kinase is mentioned: [Pg.302]    [Pg.696]    [Pg.697]    [Pg.199]    [Pg.312]    [Pg.557]    [Pg.654]    [Pg.247]    [Pg.80]    [Pg.196]    [Pg.199]    [Pg.150]    [Pg.49]    [Pg.654]    [Pg.49]    [Pg.303]    [Pg.557]    [Pg.304]    [Pg.407]    [Pg.176]    [Pg.386]    [Pg.429]    [Pg.61]    [Pg.381]    [Pg.342]   


SEARCH



3-Phosphoglycerate

Kinases phosphoglycerate kinase

Phosphoglycerate Kinase

© 2024 chempedia.info