A Disease-causing Mutation in the Active Site of Serine Palmitoyltransferase Causes Catalytic Promiscuity
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference27 articles.
1. Cloning and Initial Characterization of a New Subunit for Mammalian Serine-palmitoyltransferase
2. Identification of small subunits of mammalian serine palmitoyltransferase that confer distinct acyl-CoA substrate specificities
3. The SPTLC3 Subunit of Serine Palmitoyltransferase Generates Short Chain Sphingoid Bases
4. SPTLC1 is mutated in hereditary sensory neuropathy, type 1
5. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
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