4br1: Difference between revisions
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== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN]] Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) [MIM:[http://omim.org/entry/190450 190450]]. TPI deficiency is an autosomal recessive disorder. It is the most severe clinical disorder of glycolysis. It is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection. | [[http://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN]] Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) [MIM:[http://omim.org/entry/190450 190450]]. TPI deficiency is an autosomal recessive disorder. It is the most severe clinical disorder of glycolysis. It is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection. | ||
==See Also== | ==See Also== | ||
Revision as of 17:18, 25 December 2014
Protease-induced heterodimer of human triosephosphate isomerase.
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Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Homo sapiens
- Triose-phosphate isomerase
- Castillo-Villanueva, A
- DeLaMora-DeLaMora, I
- Enriquez-Flores, S
- Garcia-Torres, I
- Gomez-Manzo, S
- Hernandez-Alcantara, G
- Lopez-Velazquez, G
- Marcial-Quino, J
- Mendez, S T
- Mendoza-Hernandez, G
- Oria-Hernandez, J
- Reyes-Vivas, H
- Torres-Arroyo, A
- Torres-Larios, A
- Hydrolase
- Protease degradation
