ULK2

ULK2
Identifiers
AliasesULK2, ATG1B, Unc51.2, unc-51 like autophagy activating kinase 2
External IDsOMIM: 608650; MGI: 1352758; GeneCards: ULK2
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
2.7.11.1↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001142610
NM_014683

NM_013881

RefSeq (protein)

NP_001136082
NP_055498

NP_038909

Location (UCSC)Chr 17: 19.77 – 19.87 MbChr 11: 61.67 – 61.75 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Serine/threonine-protein kinase ULK2 is an enzyme which in humans is encoded by the ULK2 gene. The gene is located within the Smith–Magenis syndrome region on chromosome 17.

Structure and function

This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. ULK2 and the GTPase activating protein SynGAP function cooperatively in axon formation.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000083290 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000004798 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ↑ Yan J, Kuroyanagi H, Tomemori T, Okazaki N, Asato K, Matsuda Y, Suzuki Y, Ohshima Y, Mitani S, Masuho Y, Shirasawa T, Muramatsu M (October 1999). "Mouse ULK2, a novel member of the UNC-51-like protein kinases: unique features of functional domains". Oncogene. 18 (43): 5850–9. doi:10.1038/sj.onc.1202988. PMID 10557072.
  6. ↑ "Entrez Gene: ULK2".
  7. ↑ Tomoda T, Kim JH, Zhan C, Hatten ME (March 2004). "Role of Unc51.1 and its binding partners in CNS axon outgrowth". Genes Dev. 18 (5): 541–58. doi:10.1101/gad.1151204. PMC 374236. PMID 15014045.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.