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Reviewed, UniProtKB/Swiss-Prot Q9P2A4 (ABI3_HUMAN)

Last modified November 24, 2009. Version 69. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (6) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Binary interactions · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    ABI gene family member 3
Alternative name(s):
    New molecule including SH3
      Short name=Nesh
Gene names
Name: ABI3
Synonyms: NESH
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length366 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence 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 componentCytoplasm
   Coding sequence diversityPolymorphism
   DomainCoiled coil
SH3 domain
   PTMPhosphoprotein
   Technical termComplete proteome
Gene Ontology (GO)
   Biological processcell motion Ref.4

Non-traceable author statement. Source: UniProtKB

regulation of cell migration Ref.4

Inferred from direct assay. Source: MGI

   Cellular componentcytoplasm Ref.4

Non-traceable author statement. Source: UniProtKB

lamellipodium

Inferred from direct assay. Source: MGI

   Molecular functionprotein binding Ref.5

Non-traceable author statement. Source: UniProtKB

Complete GO annotation...

Binary interactions

With

Entry

#Exp.

IntAct

Notes

EIF3HO153722EBI-742038,EBI-709735

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 366366ABI gene family member 3
PRO_0000191792

Regions

Domain308 – 36659SH3
Coiled coil33 – 6129 Potential
Compositional bias224 – 30683Pro-rich

Natural variations

Natural variant441R → Q: dbSNP rs2233369. Ref.2
VAR_022030
Natural variant2031S → F: dbSNP rs616338.
VAR_060243

Sequences

Sequence LengthMass (Da)Tools
Q9P2A4-1 [UniParc].

Last modified October 1, 2000. Version 1.
Checksum: 1437482552CF1947

FASTA36638,975
        10         20         30         40         50         60 
MAELQQLQEF EIPTGREALR GNHSALLRVA DYCEDNYVQA TDKRKALEET MAFTTQALAS 

        70         80         90        100        110        120 
VAYQVGNLAG HTLRMLDLQG AALRQVEARV STLGQMVNMH MEKVARREIG TLATVQRLPP 

       130        140        150        160        170        180 
GQKVIAPENL PPLTPYCRRP LNFGCLDDIG HGIKDLSTQL SRTGTLSRKS IKAPATPASA 

       190        200        210        220        230        240 
TLGRPPRIPE PVHLPVVPDG RLSAASSASS LASAGSAEGV GGAPTPKGQA APPAPPLPSS 

       250        260        270        280        290        300 
LDPPPPPAAV EVFQRPPTLE ELSPPPPDEE LPLPLDLPPP PPLDGDELGL PPPPPGFGPD 

       310        320        330        340        350        360 
EPSWVPASYL EKVVTLYPYT SQKDNELSFS EGTVICVTRR YSDGWCEGVS SEGTGFFPGN 


YVEPSC 

« Hide

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. expand/collapse author list , Tampe J., Heubner D., Wambutt R., Korn B., Klein M., 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.
IPIIPI00009273.
RefSeqNP_001128658.1.
NP_057512.1.
UniGeneHs.130719

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

IntActQ9P2A4. 11 interactions.
STRINGQ9P2A4.

Proteomic databases

PRIDEQ9P2A4.

Genome annotation databases

EnsemblENST00000225941; ENSP00000225941; ENSG00000108798; Homo sapiens. [Genome view]
GeneID51225.
KEGGhsa:51225.
UCSCuc002iop.1. human.

Organism-specific databases

CTD51225.
GeneCardsGC17P044642.
H-InvDBHIX0019748.
HGNCHGNC:29859. ABI3.
MIM606363. gene.
PharmGKBPA134951642.
GenAtlasSearch...

Phylogenomic databases

HOGENOMQ9P2A4.
HOVERGENQ9P2A4.

Gene expression databases

ArrayExpressQ9P2A4.
BgeeQ9P2A4.
CleanExHS_ABI3.
GenevestigatorQ9P2A4.
GermOnlineENSG00000108798. Homo sapiens.

Family and domain databases

InterProIPR012849. Abl-interactor_HHR.
IPR001452. SH3_domain.
IPR020473. SH3_region.
[Graphical view]
PfamPF07815. Abi_HHR. 1 hit.
PF00018. SH3_1. 1 hit.
[Graphical view]
PRINTSPR00452. SH3DOMAIN.
SMARTSM00326. SH3. 1 hit.
[Graphical view]
PROSITEPS50002. SH3. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio54310.
SOURCESearch...

Entry information

Entry nameABI3_HUMAN
AccessionPrimary (citable) accession number: Q9P2A4
Secondary accession number(s): Q9H0P6
Entry history
Integrated into UniProtKB/Swiss-Prot: July 19, 2004
Last sequence update: October 1, 2000
Last modified: November 24, 2009
This is version 69 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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.

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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

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