Reviewed,
UniProtKB/Swiss-Prot Q9P2A4 (ABI3_HUMAN)
Last modified
November 24, 2009.
Version 69.
History...
Clusters with 100%,
90%,
50% identity |
Documents (6) |
Third-party data |
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Names and origin
| Protein names | Recommended name: ABI gene family member 3 Alternative name(s): New molecule including SH3 Short name=Nesh | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Complete proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 366 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at protein level. |
General annotation (Comments)
| Function | May inhibit tumor metastasis By similarity. In vitro, reduces cell motility. |
| Subunit structure | May interact with PAK1 and PAK2. Probably interacts with TARSH. Ref.5 |
| Subcellular location | Cytoplasm. Note: Colocalizes with PAK2 at leading edge of cells. Ref.4 |
| Tissue specificity | Expressed in heart, lung, liver, pancreas, kidney, placenta and at low levels in brain and skeletal muscle. Ref.1 |
| Sequence similarities | Belongs to the ABI family. Contains 1 SH3 domain. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Cytoplasm |
| Coding sequence diversity | Polymorphism |
| Domain | Coiled coil SH3 domain |
| PTM | Phosphoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Biological process | cell motion Ref.4 Non-traceable author statement. Source: UniProtKB regulation of cell migration Ref.4Inferred from direct assay. Source: MGI |
| Cellular component | cytoplasm Ref.4 Non-traceable author statement. Source: UniProtKB lamellipodiumInferred from direct assay. Source: MGI |
| Molecular function | protein binding Ref.5 Non-traceable author statement. Source: UniProtKB |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 366 | 366 | ABI gene family member 3 | PRO_0000191792 | |||||
Regions | |||||||||
| Domain | 308 – 366 | 59 | SH3 | ||||||
| Coiled coil | 33 – 61 | 29 | Potential | ||||||
| Compositional bias | 224 – 306 | 83 | Pro-rich | ||||||
Natural variations | |||||||||
| Natural variant | 44 | 1 | R → Q: dbSNP rs2233369. Ref.2 | VAR_022030 | |||||
| Natural variant | 203 | 1 | S → F: dbSNP rs616338. | VAR_060243 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Isolation and characterization of a novel human gene (NESH) which encodes a putative signaling molecule similar to e3B1 protein." Miyazaki K., Matsuda S., Ichigotani Y., Takenouchi Y., Hayashi K., Fukuda Y., Nimura Y., Hamaguchi M. Biochim. Biophys. Acta 1493:237-241(2000) [PubMed: 10978530] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY. Tissue: Placenta. |
| [2] | "Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs." Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S., Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H., Lauber J., Duesterhoeft A., Beyer A., Koehrer K., Strack N., Mewes H.-W., Ottenwaelder B., Obermaier B. Poustka A.Genome Res. 11:422-435(2001) [PubMed: 11230166] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT GLN-44. Tissue: Kidney. |
| [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: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: B-cell. |
| [4] | "Forced expression of NESH suppresses motility and metastatic dissemination of malignant cells." Ichigotani Y., Yokozaki S., Fukuda Y., Hamaguchi M., Matsuda S. Cancer Res. 62:2215-2219(2002) [PubMed: 11956071] [Abstract] Cited for: FUNCTION, PHOSPHORYLATION, SUBCELLULAR LOCATION. |
| [5] | "Cloning and sequencing of a novel human gene that encodes a putative target protein of Nesh-SH3." Matsuda S., Iriyama C., Yokozaki S., Ichigotani Y., Shirafuji N., Yamaki K., Hayakawa T., Hamaguchi M. J. Hum. Genet. 46:483-486(2001) [PubMed: 11501947] [Abstract] Cited for: INTERACTION WITH TARSH. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AB037886 mRNA. Translation: BAA90667.1. AL136709 mRNA. Translation: CAB66644.1. BC007780 mRNA. Translation: AAH07780.1. | |
| IPI | IPI00009273. |
| RefSeq | NP_001128658.1. NP_057512.1. |
| UniGene | Hs.130719 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9P2A4. 11 interactions. |
| STRING | Q9P2A4. |
Proteomic databases | |
| PRIDE | Q9P2A4. |
Genome annotation databases | |
| Ensembl | ENST00000225941; ENSP00000225941; ENSG00000108798; Homo sapiens. [Genome view] |
| GeneID | 51225. |
| KEGG | hsa:51225. |
| UCSC | uc002iop.1. human. |
Organism-specific databases | |
| CTD | 51225. |
| GeneCards | GC17P044642. |
| H-InvDB | HIX0019748. |
| HGNC | HGNC:29859. ABI3. |
| MIM | 606363. gene. |
| PharmGKB | PA134951642. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | Q9P2A4. |
| HOVERGEN | Q9P2A4. |
Gene expression databases | |
| ArrayExpress | Q9P2A4. |
| Bgee | Q9P2A4. |
| CleanEx | HS_ABI3. |
| Genevestigator | Q9P2A4. |
| GermOnline | ENSG00000108798. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR012849. Abl-interactor_HHR. IPR001452. SH3_domain. IPR020473. SH3_region. [Graphical view] |
| Pfam | PF07815. Abi_HHR. 1 hit. PF00018. SH3_1. 1 hit. [Graphical view] |
| PRINTS | PR00452. SH3DOMAIN. |
| SMART | SM00326. SH3. 1 hit. [Graphical view] |
| PROSITE | PS50002. SH3. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 54310. |
| SOURCE | Search... |
Entry information
| Entry name | ABI3_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9P2A4 Secondary accession number(s): Q9H0P6 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 17 Human chromosome 17: 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 |
| Forthcoming format changes Announcement of forthcoming format changes |

Clusters with


