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Q8TAG9 (EXOC6_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 96. 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·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Exocyst complex component 6
Alternative name(s):
Exocyst complex component Sec15A
SEC15-like protein 1
Gene names
Name:EXOC6
Synonyms:SEC15A, SEC15L, SEC15L1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length804 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

Component of the exocyst complex involved in the docking of exocytic vesicles with fusion sites on the plasma membrane. Together with RAB11A, RAB3IP, RAB8A, PARD3, PRKCI, ANXA2, CDC42 and DNMBP promotes transcytosis of PODXL to the apical membrane initiation sites (AMIS), apical surface formation and lumenogenesis By similarity.

Subunit structure

The exocyst complex is composed of EXOC1, EXOC2, EXOC3, EXOC4, EXOC5, EXOC6, EXOC7 and EXOC8. Interacts with CEP110. Interacts with RAB11A in a GTP-dependent manner By similarity. Ref.5

Sequence similarities

Belongs to the SEC15 family.

Sequence caution

The sequence AAF37262.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened.

Ontologies

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 804804Exocyst complex component 6
PRO_0000118951

Natural variations

Natural variant3961T → I. Ref.3
Corresponds to variant rs1326331 [ dbSNP | Ensembl ].
VAR_044522
Natural variant5231L → V.
Corresponds to variant rs11187225 [ dbSNP | Ensembl ].
VAR_044523
Natural variant5781T → I.
Corresponds to variant rs35647717 [ dbSNP | Ensembl ].
VAR_044524

Experimental info

Sequence conflict7761R → G in AAH28395. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q8TAG9 [UniParc].

Last modified July 22, 2008. Version 3.
Checksum: 413251A5BA6543C4

FASTA80493,722
        10         20         30         40         50         60 
MAENSESLGT VPEHERILQE IESTDTACVG PTLRSVYDDQ PNAHKKFMEK LDACIRNHDK 

        70         80         90        100        110        120 
EIEKMCNFHH QGFVDAITEL LKVRTDAEKL KVQVTDTNRR FQDAGKEVIV HTEDIIRCRI 

       130        140        150        160        170        180 
QQRNITTVVE KLQLCLPVLE MYSKLKEQMS AKRYYSALKT MEQLENVYFP WVSQYRFCQL 

       190        200        210        220        230        240 
MIENLPKLRE DIKEISMSDL KDFLESIRKH SDKIGETAMK QAQHQKTFSV SLQKQNKMKF 

       250        260        270        280        290        300 
GKNMYINRDR IPEERNETVL KHSLEEEDEN EEEILTVQDL VDFSPVYRCL HIYSVLGDEE 

       310        320        330        340        350        360 
TFENYYRKQR KKQARLVLQP QSNMHETVDG YRRYFTQIVG FFVVEDHILH VTQGLVTRAY 

       370        380        390        400        410        420 
TDELWNMALS KIIAVLRAHS SYCTDPDLVL ELKNLTVIFA DTLQGYGFPV NRLFDLLFEI 

       430        440        450        460        470        480 
RDQYNETLLK KWAGVFRDIF EEDNYSPIPV VNEEEYKIVI SKFPFQDPDL EKQSFPKKFP 

       490        500        510        520        530        540 
MSQSVPHIYI QVKEFIYASL KFSESLHRSS TEIDDMLRKS TNLLLTRTLS SCLLNLIRKP 

       550        560        570        580        590        600 
HIGLTELVQI IINTTHLEQA CKYLEDFITN ITNISQETVH TTRLYGLSTF KDARHAAEGE 

       610        620        630        640        650        660 
IYTKLNQKID EFVQLADYDW TMSEPDGRAS GYLMDLINFL RSIFQVFTHL PGKVAQTACM 

       670        680        690        700        710        720 
SACQHLSTSL MQMLLDSELK QISMGAVQQF NLDVIQCELF ASSEPVPGFQ GDTLQLAFID 

       730        740        750        760        770        780 
LRQLLDLFMV WDWSTYLADY GQPASKYLRV NPNTALTLLE KMKDTSKKNN IFAQFRKNDR 

       790        800 
DKQKLIETVV KQLRSLVNGM SQHM 

« Hide

References

« Hide 'large scale' references
[1]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]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].
[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], VARIANT ILE-396.
Tissue: Brain.
[4]"Subunit structure of the human exocyst complex."
Li C., Rodriguez M., Banerjee D.
Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 1-153.
[5]"Centriolin anchoring of exocyst and SNARE complexes at the midbody is required for secretory-vesicle-mediated abscission."
Gromley A., Yeaman C., Rosa J., Redick S., Chen C.-T., Mirabelle S., Guha M., Sillibourne J., Doxsey S.J.
Cell 123:75-87(2005) [PubMed] [Europe PMC] [Abstract]
Cited for: INTERACTION WITH CEP110.
[6]"Initial characterization of the human central proteome."
Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.
BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL358613 expand/collapse EMBL AC list , AL157705, AL392103, AL590080 Genomic DNA. Translation: CAH72805.2.
AL590080 expand/collapse EMBL AC list , AL157705, AL358613, AL392103 Genomic DNA. Translation: CAH74087.1.
AL392103 expand/collapse EMBL AC list , AL157705, AL358613, AL590080 Genomic DNA. Translation: CAI40847.2.
CH471066 Genomic DNA. Translation: EAW50083.1.
BC028395 mRNA. Translation: AAH28395.2.
AF220217 mRNA. Translation: AAF37262.1. Different initiation.
IPIIPI01013822.
RefSeqNP_001013870.1. NM_001013848.2.
NP_061926.3. NM_019053.4.
UniGeneHs.655657.

3D structure databases

ProteinModelPortalQ8TAG9.
ModBaseSearch...

Protein-protein interaction databases

IntActQ8TAG9. 10 interactions.
STRING9606.ENSP00000260762.

PTM databases

PhosphoSiteQ8TAG9.

Polymorphism databases

DMDM212287926.

Proteomic databases

PaxDbQ8TAG9.
PRIDEQ8TAG9.

Protocols and materials databases

DNASU54536.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000260762; ENSP00000260762; ENSG00000138190.
GeneID54536.
KEGGhsa:54536.
UCSCuc001kig.3. human.

Organism-specific databases

CTD54536.
GeneCardsGC10P094599.
H-InvDBHIX0009044.
HGNCHGNC:23196. EXOC6.
HPAHPA036285.
MIM609672. gene.
neXtProtNX_Q8TAG9.
PharmGKBPA134908462.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG322476.
HOGENOMHOG000290640.
HOVERGENHBG057543.
InParanoidQ8TAG9.
OrthoDBEOG4DNF3S.
PhylomeDBQ8TAG9.

Enzyme and pathway databases

Pathway_Interaction_DBarf6_traffickingpathway. Arf6 trafficking events.
insulin_pathway. Insulin Pathway.
ReactomeREACT_11123. Membrane Trafficking.
REACT_116125. Disease.

Gene expression databases

ArrayExpressQ8TAG9.
BgeeQ8TAG9.
CleanExHS_EXOC6.
GenevestigatorQ8TAG9.
GermOnlineENSG00000138190. Homo sapiens.

Family and domain databases

InterProIPR007225. Sec15.
[Graphical view]
PANTHERPTHR12702. PTHR12702. 1 hit.
PfamPF04091. Sec15. 1 hit.
[Graphical view]
PIRSFPIRSF025007. Sec15. 1 hit.
ProtoNetSearch...

Other

ChiTaRSEXOC6. human.
GenomeRNAi54536.
NextBio56960.
SOURCESearch...

Entry information

Entry nameEXOC6_HUMAN
AccessionPrimary (citable) accession number: Q8TAG9
Secondary accession number(s): Q5VXH8, Q9NZ24
Entry history
Integrated into UniProtKB/Swiss-Prot: October 25, 2002
Last sequence update: July 22, 2008
Last modified: May 1, 2013
This is version 96 of the entry and version 3 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 10

Human chromosome 10: 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