Q969Q4 (ARL11_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 92.
History...
Names·Attributes·General annotation·Ontologies·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: ADP-ribosylation factor-like protein 11 Alternative name(s): ADP-ribosylation factor-like tumor suppressor protein 1 | ||||
| Gene names |
| ||||
| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 196 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence 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 diversity | Polymorphism |
| Ligand | GTP-binding Nucleotide-binding |
| PTM | Lipoprotein Myristate Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | small GTPase mediated signal transduction Inferred from electronic annotation. Source: InterPro |
| Cellular component | intracellular Inferred from electronic annotation. Source: InterPro |
| Molecular function | GTP binding Inferred from electronic annotation. Source: UniProtKB-KW protein bindingInferred from physical interaction. Source: IntAct |
| Complete GO annotation... | |
Binary interactions
With | Entry | #Exp. | IntAct | Notes |
|---|---|---|---|---|
| TRIP13 | Q15645 | 3 | EBI-751892,EBI-358993 |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Initiator methionine | 1 | 1 | Removed Potential | ||||||
| Chain | 2 – 196 | 195 | ADP-ribosylation factor-like protein 11 | PRO_0000207479 | |||||
Regions | |||||||||
| Nucleotide binding | 19 – 26 | 8 | GTP By similarity | ||||||
| Nucleotide binding | 63 – 67 | 5 | GTP By similarity | ||||||
| Nucleotide binding | 122 – 125 | 4 | GTP By similarity | ||||||
Amino acid modifications | |||||||||
| Modified residue | 6 | 1 | Phosphoserine Ref.5 | ||||||
| Lipidation | 2 | 1 | N-myristoyl glycine Potential | ||||||
Natural variations | |||||||||
| Natural variant | 22 | 1 | S → L. Ref.1 | VAR_023742 | |||||
| Natural variant | 120 | 1 | L → M. Corresponds to variant rs35712316 [ dbSNP | Ensembl ]. | VAR_048318 | |||||
| Natural variant | 131 | 1 | P → L. Ref.1 | VAR_023743 | |||||
| Natural variant | 148 | 1 | C → R. Ref.1 Corresponds to variant rs3803185 [ dbSNP | Ensembl ]. | VAR_023744 | |||||
| Natural variant | 164 | 1 | E → K. Ref.1 | VAR_023745 | |||||
Sequences
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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. |
| IPI | IPI00056495. |
| RefSeq | NP_612459.1. NM_138450.5. |
| UniGene | Hs.558599. |
3D structure databases | |
| ProteinModelPortal | Q969Q4. |
| SMR | Q969Q4. Positions 9-174. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q969Q4. 1 interaction. |
| MINT | MINT-1441225. |
| STRING | Q969Q4. |
PTM databases | |
| PhosphoSite | Q969Q4. |
Polymorphism databases | |
| DMDM | 74751726. |
Proteomic databases | |
| PRIDE | Q969Q4. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000282026; ENSP00000282026; ENSG00000152213. |
| GeneID | 115761. |
| KEGG | hsa:115761. |
| UCSC | uc001vdf.1. human. |
Organism-specific databases | |
| CTD | 115761. |
| GeneCards | GC13P050202. |
| H-InvDB | HIX0011318. |
| HGNC | HGNC:24046. ARL11. |
| HPA | HPA040855. HPA040887. |
| MIM | 151400. phenotype. 609351. gene. |
| neXtProt | NX_Q969Q4. |
| Orphanet | 67038. Chronic B-cell lymphocytic leukemia. |
| PharmGKB | PA134974627. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG12041. |
| GeneTree | ENSGT00600000084074. |
| HOGENOM | HBG745225. |
| HOVERGEN | HBG002073. |
| InParanoid | Q969Q4. |
| OMA | EAQVVMM. |
| OrthoDB | EOG44J2KF. |
| PhylomeDB | Q969Q4. |
Gene expression databases | |
| ArrayExpress | Q969Q4. |
| Bgee | Q969Q4. |
| CleanEx | HS_ARL11. |
| Genevestigator | Q969Q4. |
| GermOnline | ENSG00000152213. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR005225. Small_GTP-bd_dom. IPR024156. Small_GTPase_ARF. IPR006689. Small_GTPase_ARF/SAR. [Graphical view] |
| KO | K07959. |
| PANTHER | PTHR11711. ARF/SAR. 1 hit. |
| Pfam | PF00025. Arf. 1 hit. [Graphical view] |
| PRINTS | PR00328. SAR1GTPBP. |
| SMART | SM00177. ARF. 1 hit. [Graphical view] |
| TIGRFAMs | TIGR00231. Small_GTP. 1 hit. |
| PROSITE | PS51417. ARF. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 79678. |
| SOURCE | Search... |
Entry information
| Entry name | ARL11_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q969Q4 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any 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 |

Clusters with