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The BioGRID Database Seperator
BioGRID Help and Support Resources
If you don't see an answer to your question listed here, please email us at: biogridadmin@gmail.com and we'll answer your question as quickly as possible. Please be advised that some of this information will change from month to month with our regular updates to our interaction data.
The BioGRID Database Seperator
Search Results Layout

The BioGRID Layout

Layout Legend
  • A - Standard annotation data for search results including official name, aliases, synonyms, organism name, and description. The color surrounding the box (in this case navy blue) represents the organism and is different for each (in this case the blue represents the organism Saccharomyces cerevisiae).
  • B - External links to 3rd party databases. These links generally point to model organism databases like SGD, MGI, FlyBase, etc. and also large genome resources such as Entrez-Gene and Ensembl.
  • C - Gene Ontology summary for the search result. If you're interested in seeing the full details for this result you can click the "view list" link to expand the GO Summary into a list of mapped GO Entries.
  • D - Click here to download a dataset consisting only of interactions listed on this search result page.
  • E - A quick summary of the number of interactions represented in the current results. In this case there are 72 protein interactions and 374 genetic interactions listed.
  • F - This drop down field, when present, allows you to switch the current view and look at the data in an alternate format.
  • G - Experimental system, Role, and Publication listings for each interaction. These results are grouped together to form a non-redundant set of results. Interactions listed in Orange denote physical experimental systems and interactions listed in green denote genetic experimental systems. All results are ordered based on confidence in the experimental systems and the number of times the interaction has been reproduced.
  • H - Annotation data for each of the resulting interactors with your search result. As above, the interface provides official names, aliases, descriptions, and Gene Ontology categories.
  • I - Each interactor is hyperlinked to allow for circular searching. Simply click on the name and you will automatically pull up all curated interactions involving that particular gene, without having to redo your keyword searching.
  • J - Sources show the first authors last name and the date in which the publication was published. You can click on these publications for more details and also to download a dataset of interactions reported by that publication.
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Experimental Systems
Each interacting partner is recorded as a gene identifier. For physical interactions this means that the article has demonstrated an interaction between a product of the bait gene and a product of the prey gene. To expedite curation we record interactors, experimental methods and pubmed ids but not other potentially useful information such as strain background, mutations, specific interaction domains or subcellular localization. Interactions reported in reviews or as unpublished data are not recorded. Self-interactions are recorded, as are reciprocal interactions if the bait-prey directionality is clear.

Interactions are recorded under the experimental systems described below:
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Physical Interactions

Affinity Capture-Luminescence - An interaction is inferred when a bait protein, tagged with luciferase, is enzymatically detected in immunoprecipitates of the prey protein as light emission. The prey protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag.

Affinity Capture-MS - An interaction is inferred when a "bait" protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.

Affinity Capture-RNA - An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and associated RNA species identified by Northern blot, RT-PCR, affinity labeling, sequencing, or microarray analysis.

Affinity Capture-Western - An interaction is inferred when a Bait protein affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.

Biochemical Activity - An interaction is inferred from the biochemical effect of one protein upon another, for example, GTP-GDP exchange activity or phosphorylation of a substrate by a kinase. The "bait" protein executes the activity on the substrate "hit" protein.

Co-crystal Structure - Interaction directly demonstrated at the atomic level by X-ray crystallography. Also used for NMR or Electron Microscopy (EM) structures. If a structure is demonstrated between 3 or more proteins, one is chosen as the bait and binary interactions are recorded between that protein and the others.

Co-fractionation - Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, one is chosen as the bait and binary interactions are recorded between that protein and the others.

Co-localization - An interaction is inferred from co-localization of two proteins in the cell, including co-dependent association of proteins with promoter DNA in chromatin immunoprecipitation experiments.

Co-purification - An interaction is inferred from the identification of two or more protein subunits in a purified protein complex, as obtained by classical biochemical fractionation or affinity purification and one or more additional fractionation steps.

Far Western - An interaction is detected between a protein immobilized on a membrane and a purified protein probe.

FRET - An interaction is inferred when close proximity of interaction partners is detected by fluorescence resonance energy transfer between pairs of fluorophore-labeled molecules, such as occurs between CFP (donor) and YFP (acceptor) fusion proteins.

PCA - A protein-protein interaction assay in which a bait protein is expressed as fusion to one of the either N- or C- terminal peptide fragments of a reporter protein and prey protein is expressed as fusion to the complementary N- or C- terminal fragment of the same reporter protein. Interaction of bait and prey proteins bring together complementary fragments, which can then fold into an active reporter.

Protein-peptide - An interaction is detected between a protein and a peptide derived from an interaction partner. This includes phage display experiments.

Protein-RNA - An interaction is detected between and protein and an RNA.

Reconstituted Complex - An interaction is detected between purified proteins in vitro.

Two-hybrid - Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.

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Genetic Interactions

Dosage Growth Defect - A genetic interaction is inferred when over expression or increased dosage of one gene causes a growth defect in a strain that is mutated or deleted for another gene.

Dosage Lethality - A genetic interaction is inferred when over expression or increased dosage of one gene causes lethality in a strain that is mutated or deleted for another gene.

Dosage Rescue - A genetic interaction is inferred when over expression or increased dosage of one gene rescues the lethality or growth defect of a strain that is mutated or deleted for another gene.

Phenotypic Enhancement - A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.

Phenotypic Suppression - A genetic interaction is inferred when mutation or over expression of one gene results in suppression of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.

Synthetic Growth Defect - A genetic interaction is inferred when mutations in separate genes, each of which alone causes a minimal phenotype, result in a significant growth defect under a given condition when combined in the same cell.

Synthetic Haploinsufficiency - A genetic interaction is inferred when mutations or deletions in separate genes, at least one of which is hemizygous, cause a minimal phenotype alone but result in lethality when combined in the same cell under a given condition.

Synthetic Lethality - A genetic interaction is inferred when mutations or deletions in separate genes, each of which alone causes a minimal phenotype, result in lethality when combined in the same cell under a given condition.

Synthetic Rescue - A genetic interaction is inferred when mutations or deletions of one gene rescues the lethality or growth defect of a strain mutated or deleted for another gene.

The BioGRID Database Seperator
Supported Identifiers for Searches
While we do support a wide variety of identifiers, our goal of limiting redundancy in our search results means that several large sequence databases such as Genbank and Ensembl do not have all their ID's available in the BioGRID. With each annotation update, our coverage increases by hundreds of thousands of new identifiers so please be patient if your ID is not currently supported. If you have a suggestion for a new identifier type, please let us know at biogridadmin@gmail.com.

The following is a listing of our currently supported identifiers:
The BioGRID Database Seperator
CDNA Accession, CDNA GI, ECOCYC, EcoGene, Ensembl, ENTREZ_GENE, ENTREZ_GENE_EG, FLYBASE, GRID_LEGACY, HGNC, HPRD, IMGT/GENE-DB, Locus Tag, MGD, MGI, MIM, Official Symbol, PROTEIN Accession, PROTEIN GI, RATMAP, RGD, SGD, Synonym, TAIR, UNIPROTKB, WormBase, Xenbase, ZFIN,
The BioGRID Database Seperator

Search Tips
The following are some suggestions that may help you find what you're looking for if you're having trouble searching:
  • Don't use ambiguous names. When possible, search for unique identifiers or systematic names. Many identifiers across the different species are duplicated, and as a result, may not uniquely identify a specific record. The more unique the identifier, the better your chance of getting a direct hit on searches.
  • Try being less specific. For example, if you searched for STE11, try searching for STE and see if more results are returned.
  • If you are searching with "ALL ORGANISMS" selected, try being more specific and choosing your organism of interest like Saccharomyces cerevisiae or Homo sapiens. Our search engine always attempt to make a direct match first, before using wild cards so, if you search for KSS for example, you may get KSS in Human when you were really after KSS1 in Yeast. Setting the organism to Saccharomyces cerevisae, however, will result in the yeast hit only.
  • Make sure you are using the correct spelling. Sounds simple, but sometimes even the publication's use the incorrect spellings.
  • Make sure and use the most common identifier when possible. Many genes have multiple synonyms but using the most common one is your best bet to find a hit.
Quick Navigation
[Search Results Layout] [Physical Interaction Definitions] [Genetic Interaction Definitions] [Supported Identifiers for Searches] [Search Tips]
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BioGRID: A General Repository for Interaction Datasets.
Chris Stark, Bobby-Joe Breitkreutz, Teresa Reguly, Lorrie Boucher, Ashton Breitkreutz, Mike Tyers.
Nucleic Acids Res. Jan 1;34:D535-9.