Concept information
Preferred term
Werner Syndrome Helicase
Type
-
mesh:Descriptor
Definition
- A DNA-dependent helicase and 3'-5' exonuclease. It has 3'->5' exonuclease activity towards double-stranded DNA with a 5'-overhang and binds preferentially to DNA substrates containing alternate secondary structures, such as replication forks and HOLLIDAY JUNCTIONS. Mutations in the WRN gene are associated with WERNER SYNDROME.
Broader concept
Synonym(s)
- RECQ3 Protein
- RECQL2 Protein
- Werner Syndrome ATP-Dependent Helicase
- Werner Syndrome RecQ-Like Helicase
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
-
Hélicase ATP-dépendante du syndrome de Werner
-
Hélicase du syndrome de Werner
-
Hélicase du syndrome de Werner semblable à RecQ
-
Protéine RECQ3
-
Protéine RECQL2
URI
http://data.loterre.fr/ark:/67375/JVR-HHKM343N-2
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