BAIT
SLC6A8
CCDS1, CRT, CRTR, CT1, CTR5
solute carrier family 6 (neurotransmitter transporter), member 8
GO Process (7)
GO Function (1)
GO Component (2)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
SORT1
Gp95, LDLCQ6, NT3
sortilin 1
GO Process (16)
GO Function (5)
GO Component (9)
Gene Ontology Biological Process
- G-protein coupled receptor signaling pathway [IMP]
- Golgi to endosome transport [IDA]
- endocytosis [IDA]
- endosome to lysosome transport [IDA]
- endosome transport via multivesicular body sorting pathway [IDA]
- extrinsic apoptotic signaling pathway via death domain receptors [IDA]
- glucose import [IMP]
- myotube differentiation [IMP]
- negative regulation of lipoprotein lipase activity [IDA]
- nerve growth factor signaling pathway [IDA]
- neuropeptide signaling pathway [IDA]
- neurotrophin TRK receptor signaling pathway [IMP]
- plasma membrane to endosome transport [IDA]
- regulation of gene expression [IMP]
- response to insulin [IMP]
- vesicle organization [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Experimental and Computational Analysis of Newly Identified Pathogenic Mutations in the Creatine Transporter SLC6A8.
Creatine is an essential metabolite for the storage and rapid supply of energy in muscle and nerve cells. In humans, impaired metabolism, transport, and distribution of creatine throughout tissues can cause varying forms of mental disability, also known as creatine deficiency syndrome (CDS). So far, 80 mutations in the creatine transporter (SLC6A8) have been associated to CDS. To better understand ... [more]
J Mol Biol Dec. 07, 2023; ();168383 [Pubmed: 38070861]
Throughput
- High Throughput
Curated By
- BioGRID