Concept information
Preferred term
Histidine Ammonia-Lyase
Type
-
mesh:Descriptor
Definition
- 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).
Broader concept
Entry terms
- 9013-75-6 (CAS RN)
- Histidase
- Histidinase
- Histidine alpha-Deaminase
- Histidine Deaminase
- L-Histidine ammonia-lyase
Allowable Qualifier(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)
In other languages
-
French
-
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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