Descriptor English: | Histidine Ammonia-Lyase | ||||||
Descriptor Spanish: |
Histidina Amoníaco-Liasa
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Descriptor Portuguese: | Histidina Amônia-Liase | ||||||
Descriptor French: | Histidine ammonia-lyase | ||||||
Entry term(s): |
Ammonia-Lyase, Histidine Deaminase, Histidine Histidase Histidinase Histidine Ammonia Lyase Histidine Deaminase Histidine alpha Deaminase Histidine alpha-Deaminase alpha-Deaminase, Histidine |
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Tree number(s): |
D08.811.520.232.400.500 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006638 | ||||||
Scope note: | 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). |
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Annotation: | /defic: consider also histidinemia (AMINO ACID METABOLISM, INBORN ERRORS) |
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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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Registry Number: | EC 4.3.1.3 | ||||||
CAS Type 1 Name: | L-Histidine ammonia-lyase | ||||||
Public MeSH Note: | 98; see HISTIDASE 1991-97, see AMMONIA-LYASES 1973-90 |
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History Note: | 98(73) |
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DeCS ID: | 6797 | ||||||
Unique ID: | D006638 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1991/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2006/07/05 |
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CHEMICALS AND DRUGS
Enzymes and Coenzymes [D08]Enzymes and Coenzymes
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Histidine Ammonia-Lyase
- Preferred
Concept UI |
M0010399 |
Scope note | 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). |
Preferred term | Histidine Ammonia-Lyase |
Entry term(s) |
Ammonia-Lyase, Histidine Deaminase, Histidine Histidase Histidinase Histidine Ammonia Lyase Histidine Deaminase Histidine alpha Deaminase Histidine alpha-Deaminase alpha-Deaminase, Histidine |
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