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Q8WVF1 (OSCP1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 74. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Protein OSCP1

Short name=hOSCP1
Alternative name(s):
Organic solute transport protein 1
Oxidored-nitro domain-containing protein 1
Gene names
Name:OSCP1
Synonyms:C1orf102, NOR1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length389 AA.
Sequence statusComplete.
Protein existenceEvidence 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 processTransport
   Cellular componentCell membrane
Membrane
   Coding sequence diversityAlternative splicing
Polymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_processtransport

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular_componentbasal 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 keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 389389Protein OSCP1
PRO_0000251965

Natural variations

Alternative sequence38 – 4710Missing in isoform 3 and isoform 4.
VSP_039475
Alternative sequence183 – 23149VSMFL…KRIEF → RECFWKHMQETVHSAQCCLP GVGNYMEDRRRRLTFHYVYP FENFEFCTWAK in isoform 4.
VSP_039476
Alternative sequence232 – 389158Missing in isoform 4.
VSP_039477
Alternative sequence329 – 37850Missing in isoform 2.
VSP_020826
Natural variant311P → R. Ref.1 Ref.6
Corresponds to variant rs11547025 [ dbSNP | Ensembl ].
VAR_027741
Natural variant1411T → A. Ref.2
Corresponds to variant rs34409118 [ dbSNP | Ensembl ].
VAR_056958
Natural variant2421K → E.
Corresponds to variant rs2359016 [ dbSNP | Ensembl ].
VAR_027742

Experimental info

Sequence conflict511D → G in BAC05326. Ref.3
Sequence conflict3171G → R in BAE16984. Ref.2
Sequence conflict3771S → G in AAL89738. Ref.1
Sequence conflict3771S → G in AAH18069. Ref.5

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified July 13, 2010. Version 4.
Checksum: 8EA5C1EF2D9973F4

FASTA38944,586
        10         20         30         40         50         60 
MSVRTLPLLF LNLGGEMLYI LDQRLRAQNI PGDKARKDEW TEVDRKRVLN DIISTMFNRK 

        70         80         90        100        110        120 
FMEELFKPQE LYSKKALRTV YERLAHASIM KLNQASMDKL YDLMTMAFKY QVLLCPRPKD 

       130        140        150        160        170        180 
VLLVTFNHLD TIKGFIRDSP TILQQVDETL RQLTEIYGGL SAGEFQLIRQ TLLIFFQDLH 

       190        200        210        220        230        240 
IRVSMFLKDK VQNNNGRFVL PVSGPVPWGT EVPGLIRMFN NKGEEVKRIE FKHGGNYVPA 

       250        260        270        280        290        300 
PKEGSFELYG DRVLKLGTNM YSVNQPVETH VSGSSKNLAS WTQESIAPNP LAKEELNFLA 

       310        320        330        340        350        360 
RLMGGMEIKK PSGPEPGFRL NLFTTDEEEE QAALTRPEEL SYEVINIQAT QDQQRSEELA 

       370        380 
RIMGEFEITE QPRLSTSKGD DLLAMMDEL 

« Hide

Isoform 2 [UniParc].

Checksum: A275B77A753D79D1
Show »

FASTA33938,810
Isoform 3 [UniParc].

Checksum: B233ECE9C1E46F08
Show »

FASTA37943,271
Isoform 4 [UniParc].

Checksum: 769226B3771F756D
Show »

FASTA22326,431

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. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., 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. expand/collapse author list , Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C., Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W., Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J., Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J., Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y., Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J., Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H., Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L., Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J., Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S., Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K., Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R., Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M., Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S., Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J., Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W., McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N., Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V., Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J., Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E., Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S., Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M., White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H., Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E., Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G., Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., 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. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., 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.
IPIIPI00154774.
IPI00335636.
IPI00409599.
IPI00969199.
RefSeqNP_659484.4. NM_145047.4.
NP_996668.1. NM_206837.2.
UniGeneHs.202207.

3D structure databases

ProteinModelPortalQ8WVF1.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000349052.

Protein family/group databases

TCDB9.B.68.1.1. putative na-independent organic solute carrier protein (OSCP1) family.

PTM databases

PhosphoSiteQ8WVF1.

Polymorphism databases

DMDM300669715.

Proteomic databases

PaxDbQ8WVF1.
PRIDEQ8WVF1.

Protocols and materials databases

DNASU127700.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000235532; ENSP00000235532; ENSG00000116885.
ENST00000315643; ENSP00000314541; ENSG00000116885.
ENST00000354267; ENSP00000346216; ENSG00000116885.
ENST00000356637; ENSP00000349052; ENSG00000116885.
GeneID127700.
KEGGhsa:127700.
UCSCuc001caq.3. human.
uc001car.3. human.
uc021olk.1. human.

Organism-specific databases

CTD127700.
GeneCardsGC01M036881.
HGNCHGNC:29971. OSCP1.
HPAHPA028436.
MIM608854. gene.
neXtProtNX_Q8WVF1.
PharmGKBPA165752125.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG307804.
HOVERGENHBG055313.
OMAGTNMYSV.

Gene expression databases

ArrayExpressQ8WVF1.
BgeeQ8WVF1.
CleanExHS_C1orf102.
GenevestigatorQ8WVF1.
GermOnlineENSG00000116885. Homo sapiens.

Family and domain databases

InterProIPR019332. OSCP1.
[Graphical view]
PfamPF10188. Oscp1. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

ChiTaRSOSCP1. human.
GenomeRNAi127700.
NextBio82166.
SOURCESearch...

Entry information

Entry nameOSCP1_HUMAN
AccessionPrimary (citable) accession number: Q8WVF1
Secondary accession number(s): A6NHM5 expand/collapse secondary AC list , A6NHS9, A6NIN9, Q4AEJ0, Q8N7G2, Q8TDF1
Entry history
Integrated into UniProtKB/Swiss-Prot: October 3, 2006
Last sequence update: July 13, 2010
Last modified: April 3, 2013
This is version 74 of the entry and version 4 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny 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