G(M2) Activator Protein [G(M2) aktivátorový protein]
- Terms
-
GM(2) Activating Protein
GM2 Activator Protein
Hexosaminidase Activator
An essential cofactor for the degradation of G(M2)GANGLIOSIDE by lysosomal BETA-N-ACETYLHEXOSAMINIDASES. Genetic mutations resulting in loss of G(M2) activator protein are one of the causes of TAY-SACHS DISEASE, AB VARIANT.
- DUI
- D049289 MeSH Browser
- CUI
- M0111676
- Previous indexing
- Proteins (1983-2004)
- History note
- 2005(1983)
- Public note
- 2005; G(M2) ACTIVATOR PROTEIN was indexed under PROTEINS 1983-2004
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AG
- agonists
- AN
- analysis
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- BL
- blood
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry 1
- CL
- classification
- DF
- deficiency
- DE
- drug effects
- EC
- economics
- GE
- genetics
- HI
- history
- IM
- immunology
- IP
- isolation & purification
- ME
- metabolism 1
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
GM2-N-acetyl-beta-D-galactosaminidase Chemical MeSH Browser