Q99884 (SC6A7_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 103.
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: Sodium-dependent proline transporter Alternative name(s): Solute carrier family 6 member 7 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 636 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | Terminates the action of proline by its high affinity sodium-dependent reuptake into presynaptic terminals. |
| Subcellular location | |
| Tissue specificity | Brain. |
| Sequence similarities | Belongs to the sodium:neurotransmitter symporter (SNF) (TC 2.A.22) family. SLC6A7 subfamily. [View classification] |
Ontologies
| Keywords | |
|---|---|
| Biological process | Amino-acid transport Neurotransmitter 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 | proline transport Traceable author statement Ref.1. Source: ProtInc transmembrane transportTraceable author statement. Source: Reactome |
| Cellular_component | integral to plasma membrane Traceable author statement Ref.1. Source: ProtInc |
| Molecular_function | neurotransmitter:sodium symporter activity Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 636 | 636 | Sodium-dependent proline transporter | PRO_0000214770 | |||||
Regions | |||||||||
| Topological domain | 1 – 45 | 45 | Cytoplasmic Potential | ||||||
| Transmembrane | 46 – 66 | 21 | Helical; Name=1; Potential | ||||||
| Transmembrane | 74 – 93 | 20 | Helical; Name=2; Potential | ||||||
| Transmembrane | 117 – 137 | 21 | Helical; Name=3; Potential | ||||||
| Topological domain | 138 – 214 | 77 | Extracellular Potential | ||||||
| Transmembrane | 215 – 233 | 19 | Helical; Name=4; Potential | ||||||
| Transmembrane | 242 – 259 | 18 | Helical; Name=5; Potential | ||||||
| Transmembrane | 295 – 312 | 18 | Helical; Name=6; Potential | ||||||
| Transmembrane | 324 – 345 | 22 | Helical; Name=7; Potential | ||||||
| Transmembrane | 378 – 397 | 20 | Helical; Name=8; Potential | ||||||
| Transmembrane | 425 – 443 | 19 | Helical; Name=9; Potential | ||||||
| Transmembrane | 459 – 479 | 21 | Helical; Name=10; Potential | ||||||
| Transmembrane | 500 – 519 | 20 | Helical; Name=11; Potential | ||||||
| Transmembrane | 538 – 556 | 19 | Helical; Name=12; Potential | ||||||
| Topological domain | 557 – 636 | 80 | Cytoplasmic Potential | ||||||
Amino acid modifications | |||||||||
| Glycosylation | 182 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 345 | 1 | L → V. Corresponds to variant rs1468564 [ dbSNP | Ensembl ]. | VAR_011390 | |||||
Experimental info | |||||||||
| Sequence conflict | 514 | 1 | M → L in AAB47007. Ref.1 | ||||||
| Sequence conflict | 514 | 1 | M → L in AAH69631. Ref.3 | ||||||
| Sequence conflict | 514 | 1 | M → L in AAH93785. Ref.3 | ||||||
| Sequence conflict | 514 | 1 | M → L in AAI13426. Ref.3 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Human brain-specific L-proline transporter: molecular cloning, functional expression, and chromosomal localization of the gene in human and mouse genomes." Shafqat S., Velaz-Faircloth M., Henzi V.A., Whitney K.D., Yang-Feng T.L., Seldin M.F., Fremeau R.T. Jr. Mol. Pharmacol. 48:219-229(1995) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Hippocampus. |
| [2] | "The DNA sequence and comparative analysis of human chromosome 5." Schmutz J., Martin J., Terry A., Couronne O., Grimwood J., Lowry S., Gordon L.A., Scott D., Xie G., Huang W., Hellsten U., Tran-Gyamfi M., She X., Prabhakar S., Aerts A., Altherr M., Bajorek E., Black S. Rubin E.M.Nature 431:268-274(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Colon. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | S80071 mRNA. Translation: AAB47007.2. AC005895 Genomic DNA. No translation available. BC069631 mRNA. Translation: AAH69631.1. BC093785 mRNA. Translation: AAH93785.1. BC113425 mRNA. Translation: AAI13426.1. |
| IPI | IPI00018537. |
| RefSeq | NP_055043.2. NM_014228.3. |
| UniGene | Hs.241597. |
3D structure databases | |
| ProteinModelPortal | Q99884. |
| SMR | Q99884. Positions 37-523. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000230671. |
PTM databases | |
| PhosphoSite | Q99884. |
Polymorphism databases | |
| DMDM | 296452899. |
Proteomic databases | |
| PaxDb | Q99884. |
| PRIDE | Q99884. |
Protocols and materials databases | |
| DNASU | 6534. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000230671; ENSP00000230671; ENSG00000011083. |
| GeneID | 6534. |
| KEGG | hsa:6534. |
| UCSC | uc003lrr.3. human. |
Organism-specific databases | |
| CTD | 6534. |
| GeneCards | GC05P149569. |
| H-InvDB | HIX0005311. |
| HGNC | HGNC:11054. SLC6A7. |
| HPA | HPA028907. |
| MIM | 606205. gene. |
| neXtProt | NX_Q99884. |
| PharmGKB | PA35914. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG0733. |
| HOGENOM | HOG000116406. |
| HOVERGEN | HBG071421. |
| InParanoid | Q99884. |
| KO | K05038. |
| OrthoDB | EOG46HG99. |
| PhylomeDB | Q99884. |
Enzyme and pathway databases | |
| Reactome | REACT_15518. Transmembrane transport of small molecules. REACT_20679. Amine compound SLC transporters. |
Gene expression databases | |
| ArrayExpress | Q99884. |
| Bgee | Q99884. |
| CleanEx | HS_SLC6A7. |
| Genevestigator | Q99884. |
| GermOnline | ENSG00000011083. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR000175. Na/ntran_symport. [Graphical view] |
| PANTHER | PTHR11616. PTHR11616. 1 hit. |
| Pfam | PF00209. SNF. 1 hit. [Graphical view] |
| PRINTS | PR00176. NANEUSMPORT. |
| PROSITE | PS00610. NA_NEUROTRAN_SYMP_1. 1 hit. PS00754. NA_NEUROTRAN_SYMP_2. 1 hit. PS50267. NA_NEUROTRAN_SYMP_3. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| DrugBank | DB00172. L-Proline. |
| GenomeRNAi | 6534. |
| NextBio | 25423. |
| SOURCE | Search... |
Entry information
| Entry name | SC6A7_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q99884 Secondary accession number(s): Q0VG81, Q52LU6 | ||||||||
| 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 5 Human chromosome 5: 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
