Malonate--CoA ligase ACSF3, mitochondrial

Summary
UniProt ID
Q4G176
Gene Symbol
  • ACSF3
Organism
Homo sapiens (human)
External Links
GlyGen
Q4G176
PubChem
Q4G176
SwissLipids
The Human Metabolome Database
HMDBP10999
The O-GlcNAc Database
Q4G176
O-GlcNAcAtlas
Q4G176
Annotation
Keyword
  • ATP-binding
  • Fatty acid metabolism
  • Ligase
  • Mitochondrion
  • Reference proteome
  • Transit peptide
Gene Ontology (GO)
Sequence
MLPHVVLTFRRLGCALASCRLAPARHRGSGLLHTAPVARSDRSAPVFTRALAFGDRIALVDQHGRHTYRELYSRSLRLSQEICRLCGCVGGDLREERVSFLCANDASYVVAQWASWMSGGVAVPLYRKHPAAQLEYVICDSQSSVVLASQEYLELLSPVVRKLGVPLLPLTPAIYTGAVEEPAEVPVPEQGWRNKGAMIIYTSGTTGRPKGVLSTHQNIRAVVTGLVHKWAWTKDDVILHVLPLHHVHGVVNALLCPLWVGATCVMMPEFSPQQVWEKFLSSETPRINVFMAVPTIYTKLMEYYDRHFTQPHAQDFLRAVCEEKIRLMVSGSAALPLPVLEKWKNITGHTLLERYGMTEIGMALSGPLTTAVRLPGSVGTPLPGVQVRIVSENPQREACSYTIHAEGDERGTKVTPGFEEKEGELLVRGPSVFREYWNKPEETKSAFTLDGWFKTGDTVVFKDGQYWIRGRTSVDIIKTGGYKVSALEVEWHLLAHPSITDVAVIGVPDMTWGQRVTAVVTLREGHSLSHRELKEWARNVLAPYAVPSELVLVEEIPRNQMGKIDKKALIRHFHPS
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
402
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Synthesis of very long-chain fatty acyl-CoAs Homo sapiens
Disease
Displaying entries 1 - 10 of 18 in total
DO ID Disease Name Source
DOID:9993 hypoglycemia
DOID:0014667 disease of metabolism
DOID:0060058 lymphoma
DOID:0111263 combined malonic and methylmalonic acidemia
DOID:10907 microcephaly
DOID:10914 amnestic disorder
DOID:13250 diarrhea
DOID:14749 methylmalonic acidemia
DOID:3234 central nervous system lymphoma
DOID:4543 retrograde amnesia

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024