Werner Syndrome Helicase [helikáza Wernerova syndromu]
- Terms
-
gen RECQL2
protein RecQ3
recQ-like helikáza Wernerova syndromu
RECQ3 gen
Wernerova helikáza
WRN gen
-
RECQ3 Protein
RECQL2 Protein
Werner Syndrome ATP-Dependent Helicase
Werner Syndrome RecQ-Like Helicase
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.
- DUI
- D000071657 MeSH Browser
- CUI
- M000615275
- Previous indexing
- Exodeoxyribonucleases (1996-2016); RecQ Helicases (2006-2016)
- History note
- 2017
- Public note
- 2017
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AN
- analysis
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- BL
- blood
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry
- CL
- classification
- DF
- deficiency
- DE
- drug effects
- EC
- economics
- GE
- genetics 1
- 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
WRN protein, Xenopus Chemical MeSH Browser
WRN protein, human Chemical MeSH Browser
WRN protein, rat Chemical MeSH Browser
Wrn protein, mouse Chemical MeSH Browser