- tyrosine metabolism
- Tyrosinstoffwechsel m
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
tyrosine metabolism
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Tyrosine — NatOrganicBox name=( S ) 2 Amino 3 (4 hydroxyphenyl) propanoic acid PubChem = 1153 CAS = 60 18 4 SMILES = N [C@@H] (Cc1ccc(O)cc1)C(O)=O C=9 | H=11 | N=1 | O=3 mass=181.19 g/molTyrosine (abbreviated as Tyr or Y) [cite web | author=IUPAC IUBMB… … Wikipedia
Tyrosine phenol-lyase — In enzymology, a tyrosine phenol lyase (EC number|4.1.99.2) is an enzyme that catalyzes the chemical reaction:L tyrosine + H2O ightleftharpoons phenol + pyruvate + NH3Thus, the two substrates of this enzyme are L tyrosine and H2O, whereas its 3… … Wikipedia
Tyrosine decarboxylase — In enzymology, a tyrosine decarboxylase (EC number|4.1.1.25) is an enzyme that catalyzes the chemical reaction:L tyrosine ightleftharpoons tyramine + CO2Hence, this enzyme has one substrate, L tyrosine, and two products, tyramine and carbon… … Wikipedia
Tyrosine 2,3-aminomutase — In enzymology, a tyrosine 2,3 aminomutase (EC number|5.4.3.6) is an enzyme that catalyzes the chemical reaction:L tyrosine ightleftharpoons 3 amino 3 (4 hydroxyphenyl)propanoateHence, this enzyme has one substrate, L tyrosine, and one product, 3… … Wikipedia
Metabolism — Cell metabolism redirects here. For the journal, see Cell Metabolism. Structure of adenosine triphosphate, a central intermediate in energy metabolism Metabolism (from Greek: μεταβολή metabolē , change or Greek: μεταβολισμός metabolismos,… … Wikipedia
Tyrosine kinase — A tyrosine kinase is an enzyme that can transfer a phosphate group from ATP to a tyrosine residue in a protein. Tyrosine kinases are a subgroup of the larger class of protein kinases. Phosphorylation of proteins by kinases is an important… … Wikipedia
List of amino acid metabolism disorders — Several genetic disorders cause errors in amino acid metabolism. Amino acid metabolism disorders result from defects either in the synthesis of or the breakdown of amino acids or in the body s ability to get the amino acids into cells. These… … Wikipedia
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
Protein tyrosine phosphatase — Protein tyrosine phosphatases (PTPs) are a group of enzymes that remove phosphate groups from phosphorylated tyrosine residues on proteins. Protein tyrosine (pTyr) phosphorylation is a common post translational modification that can create novel… … Wikipedia
Alkaptonuria — Infobox Disease Name = PAGENAME Caption = Homogentisic acid Width = 180 DiseasesDB = 409 ICD10 = ICD10|E|70|2|e|70 ICD9 = ICD9|270.2 ICDO = OMIM = 203500 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 64 MeshID = D000474 Alkaptonuria (black… … Wikipedia
tyrosinosis — A very rare, possibly heritable disorder of tyrosine metabolism that may be caused by defective formation of p hydroxyphenylpyruvic acid oxidase or of tyrosine transaminase; characterized by enhanced urinary excretion of p hydroxyphenylpyruvic… … Medical dictionary
