Concept information
Terme préférentiel
Histidine Ammonia-Lyase
Type
-
mesh:Descriptor
Définition
- An enzyme that catalyzes the first step of histidine catabolism, forming UROCANIC ACID and AMMONIA from HISTIDINE. Deficiency of this enzyme is associated with elevated levels of serum histidine and is called histidinemia (AMINO ACID METABOLISM, INBORN ERRORS).
Concept générique
Synonyme(s)
- 9013-75-6 (CAS RN)
- Histidase
- Histidinase
- Histidine alpha-Deaminase
- Histidine Deaminase
- L-Histidine ammonia-lyase
Qualificatif(s) autorisé(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- analysis (Qualifier)
- antagonists & inhibitors (Qualifier)
- biosynthesis (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemical synthesis (Qualifier)
- chemistry (Qualifier)
- classification (Qualifier)
- deficiency (Qualifier)
- drug effects (Qualifier)
- economics (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- isolation & purification (Qualifier)
- metabolism (Qualifier)
- pharmacokinetics (Qualifier)
- pharmacology (Qualifier)
- physiology (Qualifier)
- poisoning (Qualifier)
- radiation effects (Qualifier)
- standards (Qualifier)
- supply & distribution (Qualifier)
- therapeutic use (Qualifier)
- toxicity (Qualifier)
- ultrastructure (Qualifier)
- urine (Qualifier)
Traductions
-
français
-
9013-75-6 (CAS RN)
-
Histidase
-
Histidinase
-
Histidine alpha-déaminase
-
L-Histidine ammonia-lyase
URI
http://data.loterre.fr/ark:/67375/JVR-SB5Q4Q4Z-M
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