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2.A.17.4.9
Solute carrier family 15 member 1 (Intestinal H+:peptide cotransporter) (Oligopeptide transporter, small intestine isoform) (Peptide transporter 1, PepT1).  Takes up oligopeptides of 2 to 4 amino acids with a preference for dipeptides, a major route for the absorption of protein digestion end-products. PepT1 is modified by N-glycosylation, and all six asparagine residues in the large extracellular loop between TMSs 9 and 10 are subject to N-glycosylation.  This allows proper association with the plasma membrane and/or stabilization (Chan et al. 2016). Transports opioid peptides (Ganapathy and Miyauchi 2005), can serve as a druh importer and plays a role in inflammatory bowel diseases (Viennois et al. 2018). PEPT1 is upregulated in kidney cancer cell lines, with little expression in normal pancreas. PEPT1 is essential for the growth of pancreatic cancer cells and is therefore a viable drug target (Schniers et al. 2021). Mutation of arginine 282 to glutamate uncouples the movement of peptides and protons by the rabbit PepT1 (Meredith 2004). The structure of the horse ortholog shows that the extracellular domain between TMSs 9 and 10 bridges the NTD and CTD by interacting with TMS1. Deletion of ECD or mutations to the ECD-TMS1 interface impairs transport activity (Shen et al. 2022).

Accession Number:P46059
Protein Name:Solute carrier family 15 member 1
Length:708
Molecular Weight:78806.00
Species:Homo sapiens (Human) [9606]
Number of TMSs:11
Location1 / Topology2 / Orientation3: Membrane1 / Multi-pass membrane protein2
Substrate

Cross database links:

Entrez Gene ID: 6564   
Pfam: PF00854   
KEGG: hsa:6564   

Gene Ontology

GO:0005887 C:integral to plasma membrane
GO:0005624 C:membrane fraction
GO:0015333 F:peptide:hydrogen symporter activity
GO:0005427 F:proton-dependent oligopeptide secondary active transmembrane transporter activity
GO:0007586 P:digestion
GO:0015031 P:protein transport

References (5)

[1] “Human intestinal H+/peptide cotransporter. Cloning, functional expression, and chromosomal localization.”  Liang R.et.al.   7896779
[2] “The DNA sequence and analysis of human chromosome 13.”  Dunham A.et.al.   15057823
[3] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).”  The MGC Project Teamet.al.   15489334
[4] “Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population.”  Saito S.et.al.   12436193
[5] “Genetic variants of the human dipeptide transporter PEPT1.”  Anderle P.et.al.   16258023

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Predict TMSs (Predict number of transmembrane segments)
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FASTA formatted sequence
1:	MGMSKSHSFF GYPLSIFFIV VNEFCERFSY YGMRAILILY FTNFISWDDN LSTAIYHTFV 
61:	ALCYLTPILG ALIADSWLGK FKTIVSLSIV YTIGQAVTSV SSINDLTDHN HDGTPDSLPV 
121:	HVVLSLIGLA LIALGTGGIK PCVSAFGGDQ FEEGQEKQRN RFFSIFYLAI NAGSLLSTII 
181:	TPMLRVQQCG IHSKQACYPL AFGVPAALMA VALIVFVLGS GMYKKFKPQG NIMGKVAKCI 
241:	GFAIKNRFRH RSKAFPKREH WLDWAKEKYD ERLISQIKMV TRVMFLYIPL PMFWALFDQQ 
301:	GSRWTLQATT MSGKIGALEI QPDQMQTVNA ILIVIMVPIF DAVLYPLIAK CGFNFTSLKK 
361:	MAVGMVLASM AFVVAAIVQV EIDKTLPVFP KGNEVQIKVL NIGNNTMNIS LPGEMVTLGP 
421:	MSQTNAFMTF DVNKLTRINI SSPGSPVTAV TDDFKQGQRH TLLVWAPNHY QVVKDGLNQK 
481:	PEKGENGIRF VNTFNELITI TMSGKVYANI SSYNASTYQF FPSGIKGFTI SSTEIPPQCQ 
541:	PNFNTFYLEF GSAYTYIVQR KNDSCPEVKV FEDISANTVN MALQIPQYFL LTCGEVVFSV 
601:	TGLEFSYSQA PSNMKSVLQA GWLLTVAVGN IIVLIVAGAG QFSKQWAEYI LFAALLLVVC 
661:	VIFAIMARFY TYINPAEIEA QFDEDEKKNR LEKSNPYFMS GANSQKQM