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Links from Protein

Items: 8

1.

1-acyl-sn-glycerol-3-phosphate acyltransferase

This family contains acyltransferases involved in phospholipid biosynthesis and other proteins of unknown function [1]. This family also includes tafazzin Swiss:Q16635, the Barth syndrome gene [2]. [1]. 9259571. Barth syndrome may be due to an acyltransferase deficiency. Neuwald AF;. Curr Biol 1997;7:465-466. [2]. 8630491. A novel X-linked gene, G4.5. is responsible for Barth syndrome. Bione S, D'Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D;. Nat Genet 1996;12:385-389. (from Pfam)

GO Terms:
Molecular Function:
acyltransferase activity (GO:0016746)
Date:
2024-10-16
Family Accession:
NF013702.5
Method:
HMM
2.

AMP-binding protein

Date:
2024-08-14
Family Accession:
NF012711.5
Method:
HMM
3.
new record, indexing in progress
Family Accession:
4.
new record, indexing in progress
Family Accession:
5.
new record, indexing in progress
Family Accession:
6.
new record, indexing in progress
Family Accession:
7.

bifunctional acyl-ACP--phospholipid O-acyltransferase/long-chain-fatty-acid--ACP ligase

bifunctional acyl-ACP--phospholipid O-acyltransferase/long-chain-fatty-acid--ACP ligase plays a role in lysophospholipid acylation by transfering fatty acids to the 1-position via an enzyme-bound acyl-ACP intermediate

Date:
2018-11-20
Family Accession:
11483068
Method:
Sparcle
8.

bifunctional acyl-ACP--phospholipid O-acyltransferase/long-chain-fatty-acid--ACP ligase

Gene:
aas
GO Terms:
Biological Process:
fatty acid metabolic process (GO:0006631)
Biological Process:
phospholipid biosynthetic process (GO:0008654)
Molecular Function:
acyl-[acyl-carrier-protein]-phospholipid O-acyltransferase activity (GO:0008779)
Molecular Function:
long-chain fatty acid [acyl-carrier-protein] ligase activity (GO:0008922)
Date:
2021-08-30
Family Accession:
NF005959.0
Method:
HMM
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