HS1BP3

HCLS1 binding protein 3 also known as HS1BP3 is a protein which in humans is encoded by the HS1BP3 gene.[1][2]

HCLS1 binding protein 3
Identifiers
SymbolHS1BP3
NCBI gene64342
HGNC24979
OMIM609359
RefSeqNM_022460
UniProtQ53T59
Other data
LocusChr. 2 p24.1

Function

The protein encoded by this gene shares similarity with mouse Hs1bp3, an Hcls1-interacting protein that may be involved in lymphocyte activation.[3]

HS1BP3 binds members of the 14-3-3 protein family, which are highly expressed in motor neurons and Purkinje cells and regulate the Ca2+ / calmodulin-dependent protein kinase activation of tyrosine and tryptophan hydroxylase.[2]

References
  1. Takemoto Y, Furuta M, Sato M, Kubo M, Hashimoto Y (December 1999). "Isolation and characterization of a novel HS1 SH3 domain binding protein, HS1BP3". Int. Immunol. 11 (12): 1957–64. doi:10.1093/intimm/11.12.1957. PMID 10590261.
  2. Higgins JJ, Lombardi RQ, Pucilowska J, Jankovic J, Tan EK, Rooney JP (February 2005). "A variant in the HS1-BP3 gene is associated with familial essential tremor". Neurology. 64 (3): 417–21. doi:10.1212/01.WNL.0000153481.30222.38. PMC 1201396. PMID 15699368.
  3. "Entrez Gene: HCLS1 binding protein 3".

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


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