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Q969Q4 (ARL11_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 92. 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·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
ADP-ribosylation factor-like protein 11
Alternative name(s):
ADP-ribosylation factor-like tumor suppressor protein 1
Gene names
Name:ARL11
Synonyms:ARLTS1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length196 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May play a role in apoptosis. May act as a tumor suppressor. Ref.1

Tissue specificity

Expressed in lung and leukocytes. Ref.1

Involvement in disease

Defects in ARL11 may be a cause of susceptibility to chronic lymphocytic leukemia (CLL) [MIM:151400]. Ref.1

Sequence similarities

Belongs to the small GTPase superfamily. Arf family.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   LigandGTP-binding
Nucleotide-binding
   PTMLipoprotein
Myristate
Phosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processsmall GTPase mediated signal transduction

Inferred from electronic annotation. Source: InterPro

   Cellular componentintracellular

Inferred from electronic annotation. Source: InterPro

   Molecular functionGTP binding

Inferred from electronic annotation. Source: UniProtKB-KW

protein binding

Inferred from physical interaction. Source: IntAct

Complete GO annotation...

Binary interactions

With

Entry

#Exp.

IntAct

Notes

TRIP13Q156453EBI-751892,EBI-358993

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Initiator methionine11Removed Potential
Chain2 – 196195ADP-ribosylation factor-like protein 11
PRO_0000207479

Regions

Nucleotide binding19 – 268GTP By similarity
Nucleotide binding63 – 675GTP By similarity
Nucleotide binding122 – 1254GTP By similarity

Amino acid modifications

Modified residue61Phosphoserine Ref.5
Lipidation21N-myristoyl glycine Potential

Natural variations

Natural variant221S → L. Ref.1
VAR_023742
Natural variant1201L → M.
Corresponds to variant rs35712316 [ dbSNP | Ensembl ].
VAR_048318
Natural variant1311P → L. Ref.1
VAR_023743
Natural variant1481C → R. Ref.1
Corresponds to variant rs3803185 [ dbSNP | Ensembl ].
VAR_023744
Natural variant1641E → K. Ref.1
VAR_023745

Sequences

Sequence LengthMass (Da)Tools
Q969Q4 [UniParc].

Last modified December 1, 2001. Version 1.
Checksum: 99389B2A2389149E

FASTA19621,391
        10         20         30         40         50         60 
MGSVNSRGHK AEAQVVMMGL DSAGKTTLLY KLKGHQLVET LPTVGFNVEP LKAPGHVSLT 

        70         80         90        100        110        120 
LWDVGGQAPL RASWKDYLEG TDILVYVLDS TDEARLPESA AELTEVLNDP NMAGVPFLVL 

       130        140        150        160        170        180 
ANKQEAPDAL PLLKIRNRLS LERFQDHCWE LRGCSALTGE GLPEALQSLW SLLKSRSCMC 

       190 
LQARAHGAER GDSKRS 

« Hide

References

« Hide 'large scale' references
[1]"Familial cancer associated with a polymorphism in ARLTS1."
Calin G.A., Trapasso F., Shimizu M., Dumitru C.D., Yendamuri S., Godwin A.K., Ferracin M., Bernardi G., Chatterjee D., Baldassarre G., Rattan S., Alder H., Mabuchi H., Shiraishi T., Hansen L.L., Overgaard J., Herlea V., Mauro F.R. expand/collapse author list , Dighiero G., Movsas B., Rassenti L., Kipps T., Baffa R., Fusco A., Mori M., Russo G., Liu C.-G., Neuberg D., Bullrich F., Negrini M., Croce C.M.
N. Engl. J. Med. 352:1667-1676(2005) [PubMed: 15843669] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, DISEASE, VARIANTS LEU-22; LEU-131; ARG-148 AND LYS-164, FUNCTION.
Tissue: Bone marrow and Spleen.
[2]"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: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Tongue.
[3]"The DNA sequence and analysis of human chromosome 13."
Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T. expand/collapse author list , Ashwell R.I.S., Babbage A.K., Bagguley C.L., Bailey J., Bannerjee R., Barlow K.F., Bates K., Beasley H., Bird C.P., Bray-Allen S., Brown A.J., Brown J.Y., Burrill W., Carder C., Carter N.P., Chapman J.C., Clamp M.E., Clark S.Y., Clarke G., Clee C.M., Clegg S.C., Cobley V., Collins J.E., Corby N., Coville G.J., Deloukas P., Dhami P., Dunham I., Dunn M., Earthrowl M.E., Ellington A.G., Faulkner L., Frankish A.G., Frankland J., French L., Garner P., Garnett J., Gilbert J.G.R., Gilson C.J., Ghori J., Grafham D.V., Gribble S.M., Griffiths C., Hall R.E., Hammond S., Harley J.L., Hart E.A., Heath P.D., Howden P.J., Huckle E.J., Hunt P.J., Hunt A.R., Johnson C., Johnson D., Kay M., Kimberley A.M., King A., Laird G.K., Langford C.J., Lawlor S., Leongamornlert D.A., Lloyd D.M., Lloyd C., Loveland J.E., Lovell J., Martin S., Mashreghi-Mohammadi M., McLaren S.J., McMurray A., Milne S., Moore M.J.F., Nickerson T., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K.M., Rice C.M., Searle S., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Steward C.A., Sycamore N., Tester J., Thomas D.W., Tracey A., Tromans A., Tubby B., Wall M., Wallis J.M., West A.P., Whitehead S.L., Willey D.L., Wilming L., Wray P.W., Wright M.W., Young L., Coulson A., Durbin R.M., Hubbard T., Sulston J.E., Beck S., Bentley D.R., Rogers J., Ross M.T.
Nature 428:522-528(2004) [PubMed: 15057823] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Lymph.
[5]"Automated phosphoproteome analysis for cultured cancer cells by two-dimensional nanoLC-MS using a calcined titania/C18 biphasic column."
Imami K., Sugiyama N., Kyono Y., Tomita M., Ishihama Y.
Anal. Sci. 24:161-166(2008) [PubMed: 18187866] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-6, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF441378 mRNA. Translation: AAP19650.1.
AK091249 mRNA. Translation: BAC03621.1.
AL135901 Genomic DNA. Translation: CAI40715.1.
BC013150 mRNA. Translation: AAH13150.1.
IPIIPI00056495.
RefSeqNP_612459.1. NM_138450.5.
UniGeneHs.558599.

3D structure databases

ProteinModelPortalQ969Q4.
SMRQ969Q4. Positions 9-174.
ModBaseSearch...

Protein-protein interaction databases

IntActQ969Q4. 1 interaction.
MINTMINT-1441225.
STRINGQ969Q4.

PTM databases

PhosphoSiteQ969Q4.

Polymorphism databases

DMDM74751726.

Proteomic databases

PRIDEQ969Q4.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000282026; ENSP00000282026; ENSG00000152213.
GeneID115761.
KEGGhsa:115761.
UCSCuc001vdf.1. human.

Organism-specific databases

CTD115761.
GeneCardsGC13P050202.
H-InvDBHIX0011318.
HGNCHGNC:24046. ARL11.
HPAHPA040855.
HPA040887.
MIM151400. phenotype.
609351. gene.
neXtProtNX_Q969Q4.
Orphanet67038. Chronic B-cell lymphocytic leukemia.
PharmGKBPA134974627.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG12041.
GeneTreeENSGT00600000084074.
HOGENOMHBG745225.
HOVERGENHBG002073.
InParanoidQ969Q4.
OMAEAQVVMM.
OrthoDBEOG44J2KF.
PhylomeDBQ969Q4.

Gene expression databases

ArrayExpressQ969Q4.
BgeeQ969Q4.
CleanExHS_ARL11.
GenevestigatorQ969Q4.
GermOnlineENSG00000152213. Homo sapiens.

Family and domain databases

InterProIPR005225. Small_GTP-bd_dom.
IPR024156. Small_GTPase_ARF.
IPR006689. Small_GTPase_ARF/SAR.
[Graphical view]
KOK07959.
PANTHERPTHR11711. ARF/SAR. 1 hit.
PfamPF00025. Arf. 1 hit.
[Graphical view]
PRINTSPR00328. SAR1GTPBP.
SMARTSM00177. ARF. 1 hit.
[Graphical view]
TIGRFAMsTIGR00231. Small_GTP. 1 hit.
PROSITEPS51417. ARF. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio79678.
SOURCESearch...

Entry information

Entry nameARL11_HUMAN
AccessionPrimary (citable) accession number: Q969Q4
Entry history
Integrated into UniProtKB/Swiss-Prot: November 8, 2005
Last sequence update: December 1, 2001
Last modified: January 25, 2012
This is version 92 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 13

Human chromosome 13: 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