Q8WVF1 (OSCP1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 74.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Protein OSCP1 Short name=hOSCP1 Alternative name(s): Organic solute transport protein 1 Oxidored-nitro domain-containing protein 1 | ||||
| Gene names |
| ||||
| 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 | 389 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | May be involved in drug clearance in the placenta. Ref.2 |
| Subcellular location | Basal cell membrane. Note: Syncytiotrophoblast in placenta. |
| Tissue specificity | Expressed predominantly in testis, also found in placenta and to a lesser extent in thymus and small intestine; abundantly expressed in tumor-derived cell lines (Ref.2). Ubiquitously expressed (Ref.1). Ref.1 Ref.2 |
| Miscellaneous | May be involved in the development and/or progression of nosopharyngeal carcinoma. |
| Caution | The polymorphism 'Glu58Gly' (described in Ref.1) is in fact an error, the G to A change described representing a synonymous mutation that does not induce any amino acid change in Gly-32. |
| Biophysicochemical properties | Kinetic parameters: In Xenopus laevis oocytes, in a sodium-independent manner. KM=35.0 µM for p-aminohippurate (PAH) Ref.2 KM=62.3 µM for tetraethylammonium |
| Sequence caution | The sequence AAL89738.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Transport |
| Cellular component | Cell membrane Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | basal plasma membrane Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Alternative products
| This entry describes 4 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8WVF1-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q8WVF1-2) The sequence of this isoform differs from the canonical sequence as follows: 329-378: Missing. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 3 (identifier: Q8WVF1-3) The sequence of this isoform differs from the canonical sequence as follows: 38-47: Missing. | ||||||
| Isoform 4 (identifier: Q8WVF1-4) The sequence of this isoform differs from the canonical sequence as follows: 38-47: Missing. 183-231: VSMFLKDKVQ...KGEEVKRIEF → RECFWKHMQE...ENFEFCTWAK 232-389: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 389 | 389 | Protein OSCP1 | PRO_0000251965 | |||||
Natural variations | |||||||||
| Alternative sequence | 38 – 47 | 10 | Missing in isoform 3 and isoform 4. | VSP_039475 | |||||
| Alternative sequence | 183 – 231 | 49 | VSMFL…KRIEF → RECFWKHMQETVHSAQCCLP GVGNYMEDRRRRLTFHYVYP FENFEFCTWAK in isoform 4. | VSP_039476 | |||||
| Alternative sequence | 232 – 389 | 158 | Missing in isoform 4. | VSP_039477 | |||||
| Alternative sequence | 329 – 378 | 50 | Missing in isoform 2. | VSP_020826 | |||||
| Natural variant | 31 | 1 | P → R. Ref.1 Ref.6 Corresponds to variant rs11547025 [ dbSNP | Ensembl ]. | VAR_027741 | |||||
| Natural variant | 141 | 1 | T → A. Ref.2 Corresponds to variant rs34409118 [ dbSNP | Ensembl ]. | VAR_056958 | |||||
| Natural variant | 242 | 1 | K → E. Corresponds to variant rs2359016 [ dbSNP | Ensembl ]. | VAR_027742 | |||||
Experimental info | |||||||||
| Sequence conflict | 51 | 1 | D → G in BAC05326. Ref.3 | ||||||
| Sequence conflict | 317 | 1 | G → R in BAE16984. Ref.2 | ||||||
| Sequence conflict | 377 | 1 | S → G in AAL89738. Ref.1 | ||||||
| Sequence conflict | 377 | 1 | S → G in AAH18069. Ref.5 | ||||||
Sequences
| ||||||||||||||||||||||||||||||||||||
References
| « Hide 'large scale' references | |
| [1] | "Cloning, expression, and mutation analysis of NOR1, a novel human gene down-regulated in HNE-1 nasopharyngeal carcinoma cell line." Nie X., Zhang B., Li X., Xiang J., Xiao B., Ma J., Zhou M., Zhu S., Lu H., Gui R., Shen S., Li G. J. Cancer Res. Clin. Oncol. 129:410-414(2003) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 3), TISSUE SPECIFICITY, VARIANT ARG-31. |
| [2] | "Isolation and functional characterization of a novel organic solute carrier protein, hOSCP1." Kobayashi Y., Shibusawa A., Saito H., Ohshiro N., Ohbayashi M., Kohyama N., Yamamoto T. J. Biol. Chem. 280:32332-32339(2005) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 3), FUNCTION, BIOPHYSICOCHEMICAL PROPERTIES, TISSUE SPECIFICITY, VARIANT ALA-141. Tissue: Placenta. |
| [3] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2). Tissue: Testis. |
| [4] | "The DNA sequence and biological annotation of human chromosome 1." Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K. Bentley D.R.Nature 441:315-321(2006) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [6] | "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] (ISOFORM 3), VARIANT ARG-31. Tissue: Brain. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF462348 mRNA. Translation: AAL89738.1. Different initiation. AB079075 mRNA. Translation: BAE16984.1. AK098541 mRNA. Translation: BAC05326.1. AC119675 Genomic DNA. No translation available. CH471059 Genomic DNA. Translation: EAX07365.1. BC018069 mRNA. Translation: AAH18069.2. |
| IPI | IPI00154774. IPI00335636. IPI00409599. IPI00969199. |
| RefSeq | NP_659484.4. NM_145047.4. NP_996668.1. NM_206837.2. |
| UniGene | Hs.202207. |
3D structure databases | |
| ProteinModelPortal | Q8WVF1. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000349052. |
Protein family/group databases | |
| TCDB | 9.B.68.1.1. putative na-independent organic solute carrier protein (OSCP1) family. |
PTM databases | |
| PhosphoSite | Q8WVF1. |
Polymorphism databases | |
| DMDM | 300669715. |
Proteomic databases | |
| PaxDb | Q8WVF1. |
| PRIDE | Q8WVF1. |
Protocols and materials databases | |
| DNASU | 127700. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000235532; ENSP00000235532; ENSG00000116885. ENST00000315643; ENSP00000314541; ENSG00000116885. ENST00000354267; ENSP00000346216; ENSG00000116885. ENST00000356637; ENSP00000349052; ENSG00000116885. |
| GeneID | 127700. |
| KEGG | hsa:127700. |
| UCSC | uc001caq.3. human. uc001car.3. human. uc021olk.1. human. |
Organism-specific databases | |
| CTD | 127700. |
| GeneCards | GC01M036881. |
| HGNC | HGNC:29971. OSCP1. |
| HPA | HPA028436. |
| MIM | 608854. gene. |
| neXtProt | NX_Q8WVF1. |
| PharmGKB | PA165752125. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG307804. |
| HOVERGEN | HBG055313. |
| OMA | GTNMYSV. |
Gene expression databases | |
| ArrayExpress | Q8WVF1. |
| Bgee | Q8WVF1. |
| CleanEx | HS_C1orf102. |
| Genevestigator | Q8WVF1. |
| GermOnline | ENSG00000116885. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR019332. OSCP1. [Graphical view] |
| Pfam | PF10188. Oscp1. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | OSCP1. human. |
| GenomeRNAi | 127700. |
| NextBio | 82166. |
| SOURCE | Search... |
Entry information
| Entry name | OSCP1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8WVF1 Secondary accession number(s): A6NHM5 Q8TDF1 | ||||||||
| Entry history |
| ||||||||
| 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 1 Human chromosome 1: 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 |

Clusters with
