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Reviewed, UniProtKB/Swiss-Prot Q3SXY8 (AR13B_HUMAN)

Last modified July 22, 2008. Version 26. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    ADP-ribosylation factor-like protein 13B
Alternative name(s):
    ADP-ribosylation factor-like protein 2-like 1
      Short name=ARL2-like protein 1
Gene names
Name: ARL13B
Synonyms: ARL2L1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length428 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Sequence similarities

Belongs to the small GTPase superfamily. Arf family.

Ontologies

Keywords

   Coding sequence diversityAlternative splicing
   DomainCoiled coil
   LigandGTP-binding
Nucleotide-binding

Gene Ontology (GO)

None. [Check GOA]

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q3SXY8-1)

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: Q3SXY8-2)

The sequence of this isoform differs from the canonical sequence as follows:
     21-127: Missing.
Notes: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical view

Molecule processing

Chain1 – 428428ADP-ribosylation factor-like protein 13B

Regions

Nucleotide binding28 – 358GTP By similarity
Nucleotide binding71 – 755GTP By similarity
Nucleotide binding130 – 1334GTP By similarity
Coiled coil192 – 24554 Potential
Compositional bias369 – 41951Pro-rich

Natural variations

Alternative sequence21 – 127107Missing in isoform 2.

Sequences

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

Last modified October 11, 2005. Version 1.
Checksum: 002B38A38D1F7BDD

FASTA42848,643
        10         20         30         40         50         60 
MFSLMASCCG WFKRWREPVR KVTLLMVGLD NAGKTATAKG IQGEYPEDVA PTVGFSKINL 

        70         80         90        100        110        120 
RQGKFEVTIF DLGGGIRIRG IWKNYYAESY GVIFVVDSSD EERMEETKEA MSEMLRHPRI 

       130        140        150        160        170        180 
SGKPILVLAN KQDKEGALGE ADVIECLSLE KLVNEHKCLC QIEPCSAISG YGKKIDKSIK 

       190        200        210        220        230        240 
KGLYWLLHVI ARDFDALNER IQKETTEQRA LEEQEKQERA ERVRKLREER KQNEQEQAEL 

       250        260        270        280        290        300 
DGTSGLAELD PEPTNPFQPI ASVIIENEGK LEREKKNQKM EKDSDGCHLK HKMEHEQIET 

       310        320        330        340        350        360 
QGQVNHNGQK NNEFGLVENY KEALTQQLKN EDETDRPSLE SANGKKKTKK LRMKRNHRVE 

       370        380        390        400        410        420 
PLNIDDCAPE SPTPPPPPPP VGWGTPKVTR LPKLEPLGET HHNDFYRKPL PPLAVPQRPN 


SDAHDVIS 

« Hide

Isoform 2 [UniParc].

Checksum: D4D82D271E9E7F1E
Show »

32136,795

References

« Hide 'large scale' references
[1]"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] (ISOFORMS 1 AND 2).
Tissue: Brain.
[2]"Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome."
Fan Y., Esmail M.A., Ansley S.J., Blacque O.E., Boroevich K., Ross A.J., Moore S.J., Badano J.L., May-Simera H., Compton D.S., Green J.S., Lewis R.A., van Haelst M.M., Parfrey P.S., Baillie D.L., Beales P.L., Katsanis N., Davidson W.S., Leroux M.R.
Nat. Genet. 36:989-993(2004) [PubMed: 15314642] [Abstract]
Cited for: IDENTIFICATION.
+Additional computationally mapped references.

Cross-references

Sequence databases

BC094725 mRNA. Translation: AAH94725.1.
BC104035 mRNA. Translation: AAI04036.1.
BC104036 mRNA. Translation: AAI04037.1.
RefSeqNP_878899.1.
UniGeneHs.533086

3D structure databases

ModBaseSearch...

Genome annotation databases

EnsemblENSG00000169379. Homo sapiens. [Contig view]
GeneID200894.

Organism-specific databases

HGNCHGNC:25419. ARL13B.
MIM608922. gene.
PharmGKBPA134975272.
GenAtlasSearch...
GeneCardsSearch...

Phylogenomic databases

HOVERGENQ3SXY8.

Gene expression databases

ArrayExpressQ3SXY8.
CleanExHS_ARL13B.
GermOnlineENSG00000169379. Homo sapiens.

Family and domain databases

InterProIPR006689. ARF/SAR.
IPR005225. Small_GTP_bd.
[Graphical view]
PANTHERPTHR11711. ARF/SAR. 1 hit.
PfamPF00025. Arf. 1 hit.
[Graphical view]
PRINTSPR00328. SAR1GTPBP.
TIGRFAMsTIGR00231. small_GTP. 1 hit.
ProDomQ3SXY8.
[Graphical view] [Entries sharing at least one domain]
BLOCKSSearch...

Other Resources

SOURCESearch...
ProtoNetSearch...

Entry information

Entry nameAR13B_HUMAN
AccessionPrimary (citable) accession number: Q3SXY8
Secondary accession number(s): Q504W8
Entry history
Integrated into UniProtKB/Swiss-Prot: October 3, 2006
Last sequence update: October 11, 2005
Last modified: July 22, 2008
This is version 26 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

Human chromosome 3

Human chromosome 3: entries, gene names and cross-references to MIM

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

UniProtKB secondary accession numbers

Index of UniProtKB secondary accession numbers

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents