Q16348 (S15A2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 98.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Solute carrier family 15 member 2 Alternative name(s): Kidney H(+)/peptide cotransporter Oligopeptide transporter, kidney isoform Peptide transporter 2 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 729 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | Proton-coupled intake of oligopeptides of 2 to 4 amino acids with a preference for dipeptides. |
| Subcellular location | |
| Sequence similarities | Belongs to the PTR2/POT transporter (TC 2.A.17) family. [View classification] |
Ontologies
| Keywords | |
|---|---|
| Biological process | Peptide transport Protein transport Symport Transport |
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | protein transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular component | integral to plasma membrane Traceable author statement. Source: ProtInc |
| Molecular function | peptide:hydrogen symporter activity Traceable author statement. Source: ProtInc protein bindingInferred from physical interaction. Source: UniProtKB |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 729 | 729 | Solute carrier family 15 member 2 | PRO_0000064308 | |||||
Regions | |||||||||
| Transmembrane | 58 – 78 | 21 | Helical; Potential | ||||||
| Transmembrane | 88 – 108 | 21 | Helical; Potential | ||||||
| Transmembrane | 115 – 135 | 21 | Helical; Potential | ||||||
| Transmembrane | 140 – 160 | 21 | Helical; Potential | ||||||
| Transmembrane | 184 – 204 | 21 | Helical; Potential | ||||||
| Transmembrane | 218 – 238 | 21 | Helical; Potential | ||||||
| Transmembrane | 296 – 316 | 21 | Helical; Potential | ||||||
| Transmembrane | 344 – 364 | 21 | Helical; Potential | ||||||
| Transmembrane | 381 – 401 | 21 | Helical; Potential | ||||||
| Transmembrane | 568 – 588 | 21 | Helical; Potential | ||||||
| Transmembrane | 612 – 632 | 21 | Helical; Potential | ||||||
| Transmembrane | 644 – 664 | 21 | Helical; Potential | ||||||
| Transmembrane | 675 – 695 | 21 | Helical; Potential | ||||||
Amino acid modifications | |||||||||
| Glycosylation | 7 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 269 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 373 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 435 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 472 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 528 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 567 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 57 | 1 | R → H. Corresponds to variant rs1920305 [ dbSNP | Ensembl ]. | VAR_047001 | |||||
| Natural variant | 73 | 1 | Y → C. Corresponds to variant rs1143667 [ dbSNP | Ensembl ]. | VAR_047002 | |||||
| Natural variant | 350 | 1 | L → F. Corresponds to variant rs2257212 [ dbSNP | Ensembl ]. | VAR_047003 | |||||
| Natural variant | 409 | 1 | P → S. Corresponds to variant rs1143671 [ dbSNP | Ensembl ]. | VAR_047004 | |||||
| Natural variant | 509 | 1 | R → K. Corresponds to variant rs1143672 [ dbSNP | Ensembl ]. | VAR_047005 | |||||
| Natural variant | 609 | 1 | A → G. Corresponds to variant rs1143668 [ dbSNP | Ensembl ]. | VAR_047006 | |||||
| Natural variant | 609 | 1 | A → P. Corresponds to variant rs1143673 [ dbSNP | Ensembl ]. | VAR_047007 | |||||
| Natural variant | 704 | 1 | M → L. Corresponds to variant rs1920314 [ dbSNP | Ensembl ]. | VAR_047008 | |||||
Experimental info | |||||||||
| Sequence conflict | 278 – 279 | 2 | QH → HD in AAB34388. Ref.1 | ||||||
| Sequence conflict | 396 | 1 | A → R in AAB34388. Ref.1 | ||||||
| Sequence conflict | 609 | 1 | A → R in AAB34388. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | S78203 mRNA. Translation: AAB34388.1. AK289820 mRNA. Translation: BAF82509.1. CH471052 Genomic DNA. Translation: EAW79496.1. |
| IPI | IPI00328719. |
| PIR | I52481. |
| RefSeq | NP_066568.3. NM_021082.3. |
| UniGene | Hs.518089. |
3D structure databases | |
| ProteinModelPortal | Q16348. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q16348. |
PTM databases | |
| PhosphoSite | Q16348. |
Polymorphism databases | |
| DMDM | 209572672. |
Proteomic databases | |
| PRIDE | Q16348. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000489711; ENSP00000417085; ENSG00000163406. |
| GeneID | 6565. |
| KEGG | hsa:6565. |
Organism-specific databases | |
| CTD | 6565. |
| GeneCards | GC03P121612. |
| H-InvDB | HIX0024323. |
| HGNC | HGNC:10921. SLC15A2. |
| MIM | 602339. gene. |
| neXtProt | NX_Q16348. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | HBG447142. |
| HOVERGEN | HBG052962. |
| InParanoid | Q16348. |
| OMA | KCGINFS. |
| OrthoDB | EOG4Z8XW5. |
| PhylomeDB | Q16348. |
Enzyme and pathway databases | |
| Reactome | REACT_15518. Transmembrane transport of small molecules. REACT_19419. Amino acid and oligopeptide SLC transporters. |
Gene expression databases | |
| ArrayExpress | Q16348. |
| Bgee | Q16348. |
| CleanEx | HS_SLC15A2. |
| Genevestigator | Q16348. |
| GermOnline | ENSG00000163406. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR016196. MFS_dom_general_subst_transpt. IPR000109. Oligopeptide_transporter. IPR004768. Pep_H_symport. IPR018456. PTR2_symporter_CS. [Graphical view] |
| KO | K14637. |
| Pfam | PF00854. PTR2. 1 hit. [Graphical view] |
| SUPFAM | SSF103473. MFS_gen_substrate_transporter. 1 hit. |
| TIGRFAMs | TIGR00926. 2A1704. 1 hit. |
| PROSITE | PS01022. PTR2_1. 1 hit. PS01023. PTR2_2. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| DrugBank | DB01140. Cefadroxil. |
| SOURCE | Search... |
Entry information
| Entry name | S15A2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q16348 Secondary accession number(s): A8K1A5 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 3 Human chromosome 3: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with