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Q8TD91 (MAGC3_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 72. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | 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:
Melanoma-associated antigen C3
Alternative name(s):
Cancer/testis antigen 7.2
Short name=CT7.2
Hepatocellular carcinoma-associated antigen 2
MAGE-C3 antigen
Gene names
Name:MAGEC3
Synonyms:HCA2
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length643 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Tissue specificity

Expressed in testis. Not expressed in other normal tissues, but is expressed in tumors of different histological origins. Ref.4

Sequence similarities

Contains 2 MAGE domains.

Ontologies

Keywords
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainRepeat
   Molecular functionTumor antigen
   PTMPhosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q8TD91-1)

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: Q8TD91-2)

The sequence of this isoform differs from the canonical sequence as follows:
     1-76: MLLPCHWVLD...RGGTSDQRMD → MPLFPNLPRL...LPSTLILGVP
     77-374: Missing.
     577-643: PIQRPAREVL...SVMSTNFCPE → VCAGREHFIY...VFIQAIQYHP
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 643643Melanoma-associated antigen C3
PRO_0000156722

Regions

Domain184 – 384201MAGE 1
Domain456 – 643188MAGE 2
Compositional bias380 – 41536Pro-rich

Amino acid modifications

Modified residue4781Phosphothreonine Ref.5
Modified residue4841Phosphothreonine Ref.5
Modified residue4851Phosphothreonine Ref.5

Natural variations

Alternative sequence1 – 7676MLLPC…DQRMD → MPLFPNLPRLSFEEDFQNPS VTEDLVDAQDSIDEEEEDAS STSSSSFHFLFPSSSSLSSS SPLSSPLPSTLILGVP in isoform 2.
VSP_043489
Alternative sequence77 – 374298Missing in isoform 2.
VSP_043490
Alternative sequence577 – 64367PIQRP…NFCPE → VCAGREHFIYGDPRKLLTIH WVQRKYLEYREVPNSAPPRY EFLWGPRAHSEASKRSLRVF IQAIQYHP in isoform 2.
VSP_043491
Natural variant1551S → P.
Corresponds to variant rs11095909 [ dbSNP | Ensembl ].
VAR_060069
Natural variant1651L → M.
Corresponds to variant rs11095910 [ dbSNP | Ensembl ].
VAR_053505
Natural variant3071A → T.
Corresponds to variant rs176024 [ dbSNP | Ensembl ].
VAR_053506
Natural variant3281A → T.
Corresponds to variant rs176026 [ dbSNP | Ensembl ].
VAR_053507

Experimental info

Sequence conflict362 – 37413GLTEA…QKKGG → SSPLPSTLILGVP Ref.3

Sequences

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

Last modified June 1, 2002. Version 1.
Checksum: 4EB342288B3FB8A6

FASTA64371,909
        10         20         30         40         50         60 
MLLPCHWVLD ATFSDGSLGQ WVKNTCATYA LSPVVLPPQP QPRKKATDKD YSAFHLGHLR 

        70         80         90        100        110        120 
EVRLFLRGGT SDQRMDSLVL CPTYFKLWRT LSGSPGLQLS DLHFGSQPEG KFSLRRAVSV 

       130        140        150        160        170        180 
KQREEPQDWP LNEKRTLWKD SDLPTWRRGT GYTLSLPAVS PGKRLWGEKA GSLPESEPLF 

       190        200        210        220        230        240 
TYTLDEKVDK LVQFLLLKYQ AKEPLTRAEM QMNVINTYTG YFPMIFRKAR EFIEILFGIS 

       250        260        270        280        290        300 
LTEVDPDHFY VFVNTLDLTC EGSLSDEQGM PQNRLLILIL SVIFIKGNCA SEEVIWEVLN 

       310        320        330        340        350        360 
AIGPWSALAG FADVLSRLAL WESEGPEAFC EESGLRSAEG SVLDLANPQG LAGHRQEDGR 

       370        380        390        400        410        420 
RGLTEASPQQ KKGGEDEDMP AAGMPPLPQS PPEIPPQGPP KISPQGPPQS PPQSPLDSCS 

       430        440        450        460        470        480 
SPLLWTRLDE ESSSEEEDTA TWHALPESES LPRYALDEKV AELVQFLLLK YQTKEPVTKA 

       490        500        510        520        530        540 
EMLTTVIKKY KDYFPMIFGK AHEFIELIFG IALTDMDPDN HSYFFEDTLD LTYEGSLIDD 

       550        560        570        580        590        600 
QGMPKNCLLI LILSMIFIKG SCVPEEVIWE VLSAIGPIQR PAREVLEFLS KLSSIIPSAF 

       610        620        630        640 
PSWYMDALKD MEDRAQAIID TTDDATAMAS ASPSVMSTNF CPE 

« Hide

Isoform 2 [UniParc].

Checksum: DBE6CAEAB5623097
Show »

FASTA34638,906

References

« Hide 'large scale' references
[1]"Identification of genes in the chromosome X that are differentially expressed in hepatocellular carcinoma."
Dong X.-Y., Chen W.-F.
Submitted (MAR-2002) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
[2]"The DNA sequence of the human X chromosome."
Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P., Frankish A., Lovell F.L., Howe K.L., Ashurst J.L., Fulton R.S., Sudbrak R., Wen G., Jones M.C. expand/collapse author list , Hurles M.E., Andrews T.D., Scott C.E., Searle S., Ramser J., Whittaker A., Deadman R., Carter N.P., Hunt S.E., Chen R., Cree A., Gunaratne P., Havlak P., Hodgson A., Metzker M.L., Richards S., Scott G., Steffen D., Sodergren E., Wheeler D.A., Worley K.C., Ainscough R., Ambrose K.D., Ansari-Lari M.A., Aradhya S., Ashwell R.I., Babbage A.K., Bagguley C.L., Ballabio A., Banerjee R., Barker G.E., Barlow K.F., Barrett I.P., Bates K.N., Beare D.M., Beasley H., Beasley O., Beck A., Bethel G., Blechschmidt K., Brady N., Bray-Allen S., Bridgeman A.M., Brown A.J., Brown M.J., Bonnin D., Bruford E.A., Buhay C., Burch P., Burford D., Burgess J., Burrill W., Burton J., Bye J.M., Carder C., Carrel L., Chako J., Chapman J.C., Chavez D., Chen E., Chen G., Chen Y., Chen Z., Chinault C., Ciccodicola A., Clark S.Y., Clarke G., Clee C.M., Clegg S., Clerc-Blankenburg K., Clifford K., Cobley V., Cole C.G., Conquer J.S., Corby N., Connor R.E., David R., Davies J., Davis C., Davis J., Delgado O., Deshazo D., Dhami P., Ding Y., Dinh H., Dodsworth S., Draper H., Dugan-Rocha S., Dunham A., Dunn M., Durbin K.J., Dutta I., Eades T., Ellwood M., Emery-Cohen A., Errington H., Evans K.L., Faulkner L., Francis F., Frankland J., Fraser A.E., Galgoczy P., Gilbert J., Gill R., Gloeckner G., Gregory S.G., Gribble S., Griffiths C., Grocock R., Gu Y., Gwilliam R., Hamilton C., Hart E.A., Hawes A., Heath P.D., Heitmann K., Hennig S., Hernandez J., Hinzmann B., Ho S., Hoffs M., Howden P.J., Huckle E.J., Hume J., Hunt P.J., Hunt A.R., Isherwood J., Jacob L., Johnson D., Jones S., de Jong P.J., Joseph S.S., Keenan S., Kelly S., Kershaw J.K., Khan Z., Kioschis P., Klages S., Knights A.J., Kosiura A., Kovar-Smith C., Laird G.K., Langford C., Lawlor S., Leversha M., Lewis L., Liu W., Lloyd C., Lloyd D.M., Loulseged H., Loveland J.E., Lovell J.D., Lozado R., Lu J., Lyne R., Ma J., Maheshwari M., Matthews L.H., McDowall J., McLaren S., McMurray A., Meidl P., Meitinger T., Milne S., Miner G., Mistry S.L., Morgan M., Morris S., Mueller I., Mullikin J.C., Nguyen N., Nordsiek G., Nyakatura G., O'dell C.N., Okwuonu G., Palmer S., Pandian R., Parker D., Parrish J., Pasternak S., Patel D., Pearce A.V., Pearson D.M., Pelan S.E., Perez L., Porter K.M., Ramsey Y., Reichwald K., Rhodes S., Ridler K.A., Schlessinger D., Schueler M.G., Sehra H.K., Shaw-Smith C., Shen H., Sheridan E.M., Shownkeen R., Skuce C.D., Smith M.L., Sotheran E.C., Steingruber H.E., Steward C.A., Storey R., Swann R.M., Swarbreck D., Tabor P.E., Taudien S., Taylor T., Teague B., Thomas K., Thorpe A., Timms K., Tracey A., Trevanion S., Tromans A.C., d'Urso M., Verduzco D., Villasana D., Waldron L., Wall M., Wang Q., Warren J., Warry G.L., Wei X., West A., Whitehead S.L., Whiteley M.N., Wilkinson J.E., Willey D.L., Williams G., Williams L., Williamson A., Williamson H., Wilming L., Woodmansey R.L., Wray P.W., Yen J., Zhang J., Zhou J., Zoghbi H., Zorilla S., Buck D., Reinhardt R., Poustka A., Rosenthal A., Lehrach H., Meindl A., Minx P.J., Hillier L.W., Willard H.F., Wilson R.K., Waterston R.H., Rice C.M., Vaudin M., Coulson A., Nelson D.L., Weinstock G., Sulston J.E., Durbin R.M., Hubbard T., Gibbs R.A., Beck S., Rogers J., Bentley D.R.
Nature 434:325-337(2005) [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] (ISOFORM 2).
[4]"MAGE-B5, MAGE-B6, MAGE-C2, and MAGE-C3: four new members of the MAGE family with tumor-specific expression."
Lucas S., De Plaen E., Boon T.
Int. J. Cancer 87:55-60(2000) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 362-538, TISSUE SPECIFICITY.
Tissue: Blood.
[5]"Large-scale phosphoproteome analysis of human liver tissue by enrichment and fractionation of phosphopeptides with strong anion exchange chromatography."
Han G., Ye M., Zhou H., Jiang X., Feng S., Jiang X., Tian R., Wan D., Zou H., Gu J.
Proteomics 8:1346-1361(2008) [PubMed] [Europe PMC] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-478; THR-484 AND THR-485, MASS SPECTROMETRY.
Tissue: Liver.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF490508 mRNA. Translation: AAM08355.1.
AL022152, AL023279, AL049177 Genomic DNA. Translation: CAI42088.1.
AL023279, AL049177, AL022152 Genomic DNA. Translation: CAI42601.1.
AL049177, AL022152, AL023279 Genomic DNA. Translation: CAI42947.1.
AL022152 Genomic DNA. Translation: CAX15113.1.
BC103893 mRNA. Translation: AAI03894.1.
AF333706 Genomic DNA. Translation: AAK00358.1.
IPIIPI00152490.
IPI00334726.
RefSeqNP_619647.1. NM_138702.1.
NP_803251.1. NM_177456.2.
UniGeneHs.356870.

3D structure databases

ProteinModelPortalQ8TD91.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000298296.

PTM databases

PhosphoSiteQ8TD91.

Polymorphism databases

DMDM41017367.

Proteomic databases

PaxDbQ8TD91.
PRIDEQ8TD91.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000298296; ENSP00000298296; ENSG00000165509.
ENST00000409007; ENSP00000386566; ENSG00000165509.
ENST00000536088; ENSP00000441107; ENSG00000165509.
ENST00000544766; ENSP00000440444; ENSG00000165509.
GeneID139081.
KEGGhsa:139081.
UCSCuc011mwp.2. human.

Organism-specific databases

CTD139081.
GeneCardsGC0XP140926.
HGNCHGNC:23798. MAGEC3.
HPAHPA052067.
MIM300469. gene.
neXtProtNX_Q8TD91.
PharmGKBPA134916199.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG264673.
HOGENOMHOG000231161.
InParanoidQ8TD91.
OMAWVQRKYL.
OrthoDBEOG4C87S5.
PhylomeDBQ8TD91.

Gene expression databases

ArrayExpressQ8TD91.
BgeeQ8TD91.
CleanExHS_MAGEC3.
GenevestigatorQ8TD91.
GermOnlineENSG00000165509. Homo sapiens.

Family and domain databases

InterProIPR002190. MAGE.
[Graphical view]
PANTHERPTHR11736. PTHR11736. 1 hit.
PfamPF01454. MAGE. 2 hits.
[Graphical view]
PROSITEPS50838. MAGE. 2 hits.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi139081.
NextBio83890.
SOURCESearch...

Entry information

Entry nameMAGC3_HUMAN
AccessionPrimary (citable) accession number: Q8TD91
Secondary accession number(s): Q3SYA7, Q5JZ43, Q9BZ80
Entry history
Integrated into UniProtKB/Swiss-Prot: January 16, 2004
Last sequence update: June 1, 2002
Last modified: May 1, 2013
This is version 72 of the entry and version 1 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 X

Human chromosome X: 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