triosephosphate

triosephosphate
Any phosphate of a triose, but especially glycerophosphate

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  • Triosephosphate isomerase deficiency — Infobox Disease Name = Triosephosphate isomerase deficiency Caption = DiseasesDB = 30116 ICD10 = ICD10|D|55|2|d|55 ICD9 = ICD9|282.3 ICDO = OMIM = 190450 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Triosephosphate isomerase deficiency …   Wikipedia

  • Triosephosphate isomerase — Protbox Name=Triosephosphate isomerase 1 Photo=Beta barrel.png Caption=The structure of human TPI PDB|1WYI width=200 AltSymbols=TIM HGNCid=12009 Symbol=TPI1 Chromosome=12 Arm=p Band=13 LocusSupplementaryData= Gene= Gene type= Protein length=… …   Wikipedia

  • triosephosphate isomerase — An isomerizing enzyme that catalyzes the reversible interconversion of d glyceraldehyde 3 phosphate and dihydroxyacetone phosphate, a reaction of importance in glycolysis and gluconeogenesis; a deficiency of this enzyme will result in hemolytic …   Medical dictionary

  • triosephosphate dehydrogenase — tri·ose·phos·phate de·hy·dro·gen·ase (triґōs fosґfāt de hiґdro jən ās) glyceraldehyde 3 phosphate dehydrogenase …   Medical dictionary

  • TPI1 — Triosephosphate isomerase 1, also known as TPI1, is a human gene.cite web | title = Entrez Gene: TPI1 triosephosphate isomerase 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7167| accessdate = ] PBB… …   Wikipedia

  • Heterozygote advantage — A heterozygote advantage (heterozygous advantage) describes the case in which the heterozygote genotype has a higher relative fitness than either the homozygote dominant or homozygote recessive genotype. The specific case of heterozygote… …   Wikipedia

  • Methylglyoxal pathway — The methylglyoxal pathway is an offshoot of glycolysis found in some prokaryotes, which converts glucose into methylglyoxal and then into pyruvate. However unlike glycolysis the methylglyoxal pathway does not produce adenosine triphosphate, ATP.… …   Wikipedia

  • Triosephosphat-Isomerase-Defizienz — Klassifikation nach ICD 10 D55.2 Anämie durch Störungen glykolytischer Enzyme Triosephosphat Isomerase Mangel …   Deutsch Wikipedia

  • Calvin-Zyklus — Übergeordnet Dunkelreaktion Kohlenstoffdioxid Assimilation Gene Ontology …   Deutsch Wikipedia

  • НЕДОСТАТОЧНОСТЬ ФЕРМЕНТОВ — мед. Синдромы врождённых нарушений обмена веществ встречаются редко, но оказывают значительное влияние на физическое, интеллектуальное, психическое развитие и качество жизни (например, фенилкетонурия, гомоцистинурия, гликогенозы, синдромы ломкой… …   Справочник по болезням

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