sphinganine kinase
Identifiers
EC no.2.7.1.91
CAS no.50864-48-7
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins
sphingosine kinase 1
Sphingosine kinase 1, hexamer, Human
Identifiers
SymbolSPHK1
NCBI gene8877
HGNC11240
OMIM603730
RefSeqNM_182965
UniProtQ9NYA1
Other data
EC number2.7.1.91
LocusChr. 17 q25.2
Search for
StructuresSwiss-model
DomainsInterPro
sphingosine kinase 2
Identifiers
SymbolSPHK2
NCBI gene56848
HGNC18859
OMIM607092
RefSeqNM_020126
UniProtQ9NRA0
Other data
EC number2.7.1.91
LocusChr. 19 q13.2
Search for
StructuresSwiss-model
DomainsInterPro

Sphingosine kinase (SphK) is a conserved lipid kinase that catalyzes formation sphingosine-1-phosphate (S1P) from the precursor sphingolipid sphingosine. Sphingolipid metabolites, such as ceramide, sphingosine and sphingosine-1-phosphate, are lipid second messengers involved in diverse cellular processes. There are two forms of SphK, SphK1 and SphK2. SphK1 is found in the cytosol of eukaryotic cells, and migrates to the plasma membrane upon activation. SphK2 is localized to the nucleus.

Function

S1P has been shown to regulate diverse cellular processes. It has been characterized as a lipid signaling molecule with dual function. On one hand, it exerts its actions extracellularly by binding to the five different S1P receptors that couple to a variety of G-proteins to regulate diverse biological functions, ranging from cell growth and survival to effector functions, such as proinflammatory mediator synthesis. On the other hand, it appears to act as an intracellular second messenger,[1] although the relevant molecular target(s) to which it binds within cells remains to be discovered. The role of S1P in various functions of cells and tissues is established, including regulation of cell survival and motility, angiogenesis, and inflammatory responses. Sphingosine kinases (SphKs) types 1 and 2, the two enzymes identified so far in mammals that produce S1P by ATP-dependent phosphorylation of sphingosine, have therefore received considerable interest.[2]

Sphingolipid metabolism

Sphingolipids are ubiquitous membrane constituents of all eukaryotic cells. In general, the term sphingolipid (SL) refers to any of a number of lipids consisting of a head group attached to the 1-OH of ceramide (Cer). Ceramides consist of a sphingoid base, commonly referred to as a long-chain base (LCB), which is N-acylated. De novo synthesis of LCBs begins with the condensation of palmitoyl-CoA with serine, forming 3-ketosphinganine (Fig. 1). This product is then reduced to sphinganine, also known as dihydrosphingosine (dihydro-Sph; 2-amino-1,3-dihydroxy-octadecane). A 14– to 26-carbon fatty acid chain is then added in an amide linkage with the 2-amino group, forming dihydroceramide (dihydro-Cer). A head group, such as phosphocholine or a carbohydrate, can now be added to the 1-OH, forming a sphingolipid, although most sphingolipids of higher eukaryotes contain further modifications of the LCB.[3]

De novo synthesis

During "100,000 Airplanes", a third season episode of The West Wing, sphingosine kinase is fictitiously described as "the enzyme believed to control all signal pathways to cancer growth." Learning of it inspires the protagonist of the series, President Josiah Bartlet, to consider launching an Apollo program to cure cancer.

References

  1. ↑ Olivera A, Spiegel S (April 2001). "Sphingosine kinase: a mediator of vital cellular functions". Prostaglandins Other Lipid Mediat. 64 (1–4): 123–34. doi:10.1016/S0090-6980(01)00108-3. PMID 11324702.
  2. ↑ Billich A, Bornancin F, Mechtcheriakova D, Natt F, Huesken D, Baumruker T (October 2005). "Basal and induced sphingosine kinase 1 activity in A549 carcinoma cells: function in cell survival and IL-1beta and TNF-alpha induced production of inflammatory mediators". Cell. Signal. 17 (10): 1203–17. doi:10.1016/j.cellsig.2004.12.005. PMID 16038795.
  3. ↑ Maceyka M, Milstien S, Spiegel S (September 2005). "Sphingosine kinases, sphingosine-1-phosphate and sphingolipidomics". Prostaglandins Other Lipid Mediat. 77 (1–4): 15–22. doi:10.1016/j.prostaglandins.2004.09.010. PMID 16099387.

Further reading

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