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Q6BDI9 (REP15_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 48. 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·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Rab15 effector protein
Gene names
Name:REP15
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length236 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

Regulates transferrin receptor recycling from the endocytic recycling compartment. Ref.3

Subunit structure

Interacts with the GTP-bound form of RAB15. Ref.3

Subcellular location

Early endosome membrane. Note: Colocalizes with RAB11 and RAB15 to the endocytic recycling compartment. Ref.3

Sequence caution

The sequence AAT76304.1 differs from that shown. Reason: Contaminating sequence. Sequence of unknown origin in the N-terminal part.

Ontologies

Keywords
   Cellular componentEndosome
Membrane
   Coding sequence diversityPolymorphism
   PTMLipoprotein
Myristate
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular_componentearly endosome membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Initiator methionine11Removed Potential
Chain2 – 236235Rab15 effector protein
PRO_0000323587

Amino acid modifications

Lipidation21N-myristoyl glycine Potential

Natural variations

Natural variant1011N → D. Ref.2 Ref.3
Corresponds to variant rs929949 [ dbSNP | Ensembl ].
VAR_039548
Natural variant2061E → D.
Corresponds to variant rs12819160 [ dbSNP | Ensembl ].
VAR_039549

Experimental info

Sequence conflict881L → P in AAT76304. Ref.3
Sequence conflict1141Q → R in AAT76304. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q6BDI9 [UniParc].

Last modified January 11, 2011. Version 4.
Checksum: BE81DA3B710C25DC

FASTA23626,571
        10         20         30         40         50         60 
MGQKASQQLA LKDSKEVPVV CEVVSEAIVH AAQKLKEYLG FEYPPSKLCP AANTLNEIFL 

        70         80         90        100        110        120 
IHFITFCQEK GVDEWLTTTK MTKHQAFLFG ADWIWTFWGS NKQIKLQLAV QTLQMSSPPP 

       130        140        150        160        170        180 
VESKPCDLSN PESRVEESSW KKSRFDKLEE FCNLIGEDCL GLFIIFGMPG KPKDIRGVVL 

       190        200        210        220        230 
DSVKSQMVRS HLPGGKAVAQ FVLETEDCVF IKELLRNCLS KKDGLREVGK VYISIL 

« Hide

References

« Hide 'large scale' references
[1]"The finished DNA sequence of human chromosome 12."
Scherer S.E., Muzny D.M., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J., Jackson A., Khan Z.M., Kovar-Smith C., Lewis L.R. expand/collapse author list , Lozado R.J., Metzker M.L., Milosavljevic A., Miner G.R., Montgomery K.T., Morgan M.B., Nazareth L.V., Scott G., Sodergren E., Song X.-Z., Steffen D., Lovering R.C., Wheeler D.A., Worley K.C., Yuan Y., Zhang Z., Adams C.Q., Ansari-Lari M.A., Ayele M., Brown M.J., Chen G., Chen Z., Clerc-Blankenburg K.P., Davis C., Delgado O., Dinh H.H., Draper H., Gonzalez-Garay M.L., Havlak P., Jackson L.R., Jacob L.S., Kelly S.H., Li L., Li Z., Liu J., Liu W., Lu J., Maheshwari M., Nguyen B.-V., Okwuonu G.O., Pasternak S., Perez L.M., Plopper F.J.H., Santibanez J., Shen H., Tabor P.E., Verduzco D., Waldron L., Wang Q., Williams G.A., Zhang J., Zhou J., Allen C.C., Amin A.G., Anyalebechi V., Bailey M., Barbaria J.A., Bimage K.E., Bryant N.P., Burch P.E., Burkett C.E., Burrell K.L., Calderon E., Cardenas V., Carter K., Casias K., Cavazos I., Cavazos S.R., Ceasar H., Chacko J., Chan S.N., Chavez D., Christopoulos C., Chu J., Cockrell R., Cox C.D., Dang M., Dathorne S.R., David R., Davis C.M., Davy-Carroll L., Deshazo D.R., Donlin J.E., D'Souza L., Eaves K.A., Egan A., Emery-Cohen A.J., Escotto M., Flagg N., Forbes L.D., Gabisi A.M., Garza M., Hamilton C., Henderson N., Hernandez O., Hines S., Hogues M.E., Huang M., Idlebird D.G., Johnson R., Jolivet A., Jones S., Kagan R., King L.M., Leal B., Lebow H., Lee S., LeVan J.M., Lewis L.C., London P., Lorensuhewa L.M., Loulseged H., Lovett D.A., Lucier A., Lucier R.L., Ma J., Madu R.C., Mapua P., Martindale A.D., Martinez E., Massey E., Mawhiney S., Meador M.G., Mendez S., Mercado C., Mercado I.C., Merritt C.E., Miner Z.L., Minja E., Mitchell T., Mohabbat F., Mohabbat K., Montgomery B., Moore N., Morris S., Munidasa M., Ngo R.N., Nguyen N.B., Nickerson E., Nwaokelemeh O.O., Nwokenkwo S., Obregon M., Oguh M., Oragunye N., Oviedo R.J., Parish B.J., Parker D.N., Parrish J., Parks K.L., Paul H.A., Payton B.A., Perez A., Perrin W., Pickens A., Primus E.L., Pu L.-L., Puazo M., Quiles M.M., Quiroz J.B., Rabata D., Reeves K., Ruiz S.J., Shao H., Sisson I., Sonaike T., Sorelle R.P., Sutton A.E., Svatek A.F., Svetz L.A., Tamerisa K.S., Taylor T.R., Teague B., Thomas N., Thorn R.D., Trejos Z.Y., Trevino B.K., Ukegbu O.N., Urban J.B., Vasquez L.I., Vera V.A., Villasana D.M., Wang L., Ward-Moore S., Warren J.T., Wei X., White F., Williamson A.L., Wleczyk R., Wooden H.S., Wooden S.H., Yen J., Yoon L., Yoon V., Zorrilla S.E., Nelson D., Kucherlapati R., Weinstock G., Gibbs R.A.
Nature 440:346-351(2006) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]"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 ASP-101.
Tissue: Testis.
[3]"Rab15 effector protein: a novel protein for receptor recycling from the endocytic recycling compartment."
Strick D.J., Elferink L.A.
Mol. Biol. Cell 16:5699-5709(2005) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 4-236, FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH THE GTP-BOUND FORM OF RAB15, VARIANT ASP-101.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AC009509 Genomic DNA. No translation available.
BC140921 mRNA. Translation: AAI40922.1.
AY662682 mRNA. Translation: AAT76304.1. Sequence problems.
IPIIPI00465270.
RefSeqNP_001025045.1. NM_001029874.1.
UniGeneHs.269836.

3D structure databases

ProteinModelPortalQ6BDI9.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000310335.

Polymorphism databases

DMDM205371860.

Proteomic databases

PaxDbQ6BDI9.
PRIDEQ6BDI9.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000310791; ENSP00000310335; ENSG00000174236.
GeneID387849.
KEGGhsa:387849.
UCSCuc001rig.1. human.

Organism-specific databases

CTD387849.
GeneCardsGC12P027849.
H-InvDBHIX0036773.
HGNCHGNC:33748. REP15.
HPAHPA040448.
MIM610848. gene.
neXtProtNX_Q6BDI9.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG26651.
HOGENOMHOG000154091.
HOVERGENHBG108401.
InParanoidQ6BDI9.
OMAFGADWIW.
OrthoDBEOG4933JR.
PhylomeDBQ6BDI9.

Gene expression databases

BgeeQ6BDI9.
GenevestigatorQ6BDI9.

Family and domain databases

ProtoNetSearch...

Other

GenomeRNAi387849.
NextBio101671.
SOURCESearch...

Entry information

Entry nameREP15_HUMAN
AccessionPrimary (citable) accession number: Q6BDI9
Secondary accession number(s): B2RU16
Entry history
Integrated into UniProtKB/Swiss-Prot: March 18, 2008
Last sequence update: January 11, 2011
Last modified: April 3, 2013
This is version 48 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 12

Human chromosome 12: 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