Homo sapiens Protein: GLYATL2
Summary
InnateDB Protein IDBP-47972.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GLYATL2
Protein Name glycine-N-acyltransferase-like 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000287275
InnateDB Gene IDBG-47970 (GLYATL2)
Protein Structure
UniProt Annotation
Function Mitochondrial acyltransferase which transfers the acyl group to the N-terminus of glycine. Conjugates numerous substrates, such as arachidonoyl-CoA and saturated medium and long-chain acyl-CoAs ranging from chain-length C8:0-CoA to C18:0- CoA, to form a variety of N-acylglycines. Shows a preference for monounsaturated fatty acid oleoyl-CoA (C18:1-CoA) as an acyl donor. Does not exhibit any activity toward C22:6-CoA and chenodeoxycholoyl-CoA, nor toward serine or alanine. {ECO:0000269PubMed:20305126}.
Subcellular Localization Endoplasmic reticulum {ECO:0000269PubMed:20305126}.
Disease Associations
Tissue Specificity Expressed at highest levels in salivary gland and trachea. Also detected in thyroid gland, spinal cord, prostate, lung and fetal brain. {ECO:0000269PubMed:20305126}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
GO:0047961 glycine N-acyltransferase activity
Biological Process
GO:0008152 metabolic process
Cellular Component
GO:0005739 mitochondrion
GO:0005783 endoplasmic reticulum
Protein Structure and Domains
PDB ID
InterPro IPR013652 Glycine N-acyltransferase, C-terminal
IPR013653 FR47-like
IPR015938 Glycine N-acyltransferase, N-terminal
IPR016181 Acyl-CoA N-acyltransferase
PFAM PF08444
PF08445
PF06021
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WU03
PhosphoSite PhosphoSite-Q8WU03
TrEMBL A0A024R4Z5
UniProt Splice Variant
Entrez Gene 219970
UniGene Hs.254271
RefSeq NP_659453
HUGO HGNC:24178
OMIM 614762
CCDS CCDS41649
HPRD 16568
IMGT
EMBL AB207211 AF426250 BC016789 BC021682 CH471076
GenPept AAH16789 AAH21682 AAO73139 BAF63415 EAW73826 EAW73827