Version 5.4
Bos taurus Protein: BT.56096
Summary
InnateDB Protein IDBP-698558.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.56096
Protein Name ras association domain-containing protein 1
Synonyms
Species Bos taurus
Ensembl Protein ENSBTAP00000027919
InnateDB Gene IDBG-645805 (BT.56096)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 49 interaction(s) predicted by orthology.
Predicted by orthology
Total 49 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0042802 identical protein binding
GO:0047485 protein N-terminus binding
Biological Process
GO:0006974 cellular response to DNA damage stimulus
GO:0007050 cell cycle arrest
GO:0007165 signal transduction
GO:0007265 Ras protein signal transduction
GO:0031398 positive regulation of protein ubiquitination
GO:0050821 protein stabilization
GO:0071157 negative regulation of cell cycle arrest
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0015630 microtubule cytoskeleton
Protein Structure and Domains
PDB ID
InterPro IPR000159 Ras-association
IPR011524 SARAH domain
IPR029071 Ubiquitin-related domain
PFAM PF00788
PRINTS
PIRSF
SMART SM00314
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-
TrEMBL F1MC29
UniProt Splice Variant
Entrez Gene 510276
UniGene Bt.56096
RefSeq NP_001068910
HUGO HGNC:9882
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02054410
GenPept

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca