fumarase
1013-Methylglutaconic aciduria — Classification and external resources 3 methylglutaconic acid DiseasesDB …
1023-Methylcrotonyl-CoA carboxylase deficiency — Classification and external resources Methylcrotonyl CoA OMIM 210200 …
103Methylmalonyl-CoA mutase deficiency — Classification and external resources OMIM 251000 DiseasesDB 29509 Methylmalonyl CoA mutase deficiency ( MUT ) is an inborn error of organ …
104Pyruvate dehydrogenase deficiency — Classification and external resources ICD 10 E74.4 ICD 9 271.8 …
105D-Glyceric acidemia — Classification and external resources OMIM 220120 D Glyceric Acidemia (a.k.a. D Glyceric Aciduria) is an inherited disease, in the category of inborn errors of metabolism. It is caused by a mutation in the gene GLYCTK, which encodes the for the… …
106Monoamine oxidase A — Ribbon diagram of an MAO A monomer, with FAD and clorgiline bound, oriented as if attached to the outer membrane of a mitochondrion …
107Porphobilinogen synthase — Identifiers EC number 4.2.1.24 CAS number 9036 37 7 …
108N-Acetylglutamate synthase — Identifiers Symbol NAGS Entrez 162417 HUGO …
109Oculocerebrorenal syndrome — Classification and external resources ICD 10 E72.0 ICD 9 270.8 …
110Catalytically perfect enzyme — A catalytically perfect enzyme or kinetically perfect enzyme is an enzyme that catalyzes so efficiently, that almost every time enzyme meets its substrate, the reaction occurs. k cat/ K m factor of such enzyme is of order 108 to 109 M 1 s 1. Such …