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. Author manuscript; available in PMC: 2013 Jun 22.
Published in final edited form as: Biochem J. 2012 Feb 1;441(3):789–802. doi: 10.1042/BJ20111626

Table 3. CerS substrate preferences.

dHSph, dihydrosphingosine.

Acyl-CoA preference*
CerS In vitro Gain of function Loss of function Km towards dHSph (μM)§ Reference(s)
CerS1 C18:0 C18:0 C18:0 2.5 ± 0.7 [21,33,38,80]
C20:0 C18:1
CerS2 C20:0 C20:0 C22:0 4.8 ± 0.4 [20,33,40,92]
C22:0 C22:0 C22:1
C24:0 C24:0 C24:0
C26:0 C24:1 C24:1
C26:0 C26:0
C26:1 C26:1
CerS3 C16:0 C18:0 1.7 ± 0.4 [23]
C18:0 C20:0
C22:0 C22:0
C24:0 C24:0
CerS4 C18:0 C18:0 C24:1 1.8 ± 0.4 [22,33,92]
C20:0 C20:0
C22:0 C22:0
C24:0
C26:0
CerS5 C14:0 C16:0 C16:0 1.8 ± 0.4 [22,25,90]
C16:0 C18:0
C18:0
C18:1
CerS6 C14:0 C16:0 C16:0 2.0 ± 0.6 [33,93,94]
C16:0
C18:0
*

Bold chain lengths indicate the primary N-acyl length affected in each experimental situation.

Determined by overexpression of CerS proteins and measurement of ceramide or other sphingolipids.

Determined by siRNA-mediated knockdown or knockout of the indicated CerS.

§

Values taken from Lahiri et al. [43].

Recent results from Jennemann et al. [90a] show that CerS3-deficient animals lack ultra-long ceramides (>C26) in the epidermis.