4omt | pdb_00004omt
From Proteopedia
Crystallization and preliminary crystallographic analysis of human muscle phosphofructokinase, the main regulator of glycolysis
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Structural highlights
Disease[K6PF_HUMAN] Glycogen storage disease due to muscle phosphofructokinase deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function[K6PF_HUMAN] Catalyzes the third step of glycolysis, the phosphorylation of fructose-6-phosphate (F6P) by ATP to generate fructose-1,6-bisphosphate (FBP) and ADP.[HAMAP-Rule:MF_00339] Contents | ||||||||||||||||||||
This page was last modified 07:27, 14 May 2014.