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A protein domain-based interactome network for C. elegans early embryogenesis.

Cell | 2008

Many protein-protein interactions are mediated through independently folding modular domains. Proteome-wide efforts to model protein-protein interaction or "interactome" networks have largely ignored this modular organization of proteins. We developed an experimental strategy to efficiently identify interaction domains and generated a domain-based interactome network for proteins involved in C. elegans early-embryonic cell divisions. Minimal interacting regions were identified for over 200 proteins, providing important information on their domain organization. Furthermore, our approach increased the sensitivity of the two-hybrid system, resulting in a more complete interactome network. This interactome modeling strategy revealed insights into C. elegans centrosome function and is applicable to other biological processes in this and other organisms.

Pubmed ID: 18692475 RIS Download

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R21CA113711
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-06
  • Agency: NCI NIH HHS, United States
    Id: R21 CA113711-01A2
  • Agency: NCI NIH HHS, United States
    Id: R33CA81658
  • Agency: NCI NIH HHS, United States
    Id: R33 CA105405-02
  • Agency: NHGRI NIH HHS, United States
    Id: R01HG001715
  • Agency: NCI NIH HHS, United States
    Id: R33 CA081658-04
  • Agency: NCRR NIH HHS, United States
    Id: R21RR023114
  • Agency: NCI NIH HHS, United States
    Id: P01 CA095281-01A10004
  • Agency: NCI NIH HHS, United States
    Id: U54 CA011295
  • Agency: NCI NIH HHS, United States
    Id: P01 CA095281
  • Agency: NCI NIH HHS, United States
    Id: U54 CA112952-01
  • Agency: NCI NIH HHS, United States
    Id: U54 CA112952-02
  • Agency: NCRR NIH HHS, United States
    Id: R21 RR023114-02
  • Agency: NCRR NIH HHS, United States
    Id: R21 RR023114
  • Agency: NCRR NIH HHS, United States
    Id: R21 RR023114-01
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-07
  • Agency: NCI NIH HHS, United States
    Id: CA95281
  • Agency: NCI NIH HHS, United States
    Id: U54 CA112952-03
  • Agency: NCI NIH HHS, United States
    Id: R33 CA105405-03
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715
  • Agency: NCI NIH HHS, United States
    Id: R33CA105405
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-09
  • Agency: NCI NIH HHS, United States
    Id: R33 CA105405
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-10
  • Agency: NCI NIH HHS, United States
    Id: U54 CA112952
  • Agency: NCI NIH HHS, United States
    Id: R21 CA113711
  • Agency: NCI NIH HHS, United States
    Id: R33 CA105405-01
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-07S1
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG001715-08

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This is a list of tools and resources that we have found mentioned in this publication.


Gene Ontology (tool)

RRID:SCR_002811

Computable knowledge regarding functions of genes and gene products. GO resources include biomedical ontologies that cover molecular domains of all life forms as well as extensive compilations of gene product annotations to these ontologies that provide largely species-neutral, comprehensive statements about what gene products do. Used to standardize representation of gene and gene product attributes across species and databases.

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Gene Expression Profiling in Spinal Cord Injury (tool)

RRID:SCR_003260

Database which provides on-line searching of microarray datasets generated from rat spinal cord after contusion injury. Both the primary injury site and a site 5 mm distal to the injury site were assayed. Tissue was obtained from Long Evans rats subject to spinal cord contusion injury using the MASCIS impactor (formerly known as the NYU impactor). RNA expression was assayed at the site of injury and distal to the site of injury using the Affymetrix Rat Neuro U34 chip.

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Hmmer (tool)

RRID:SCR_005305

Tool for searching sequence databases for homologs of protein sequences, and for making protein sequence alignments. It implements methods using probabilistic models called profile hidden Markov models (profile HMMs). Compared to BLAST, FASTA, and other sequence alignment and database search tools based on older scoring methodology, HMMER aims to be significantly more accurate and more able to detect remote homologs because of the strength of its underlying mathematical models. In the past, this strength came at significant computational expense, but in the new HMMER3 project, HMMER is now essentially as fast as BLAST.

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InterPro (tool)

RRID:SCR_006695

Service providing functional analysis of proteins by classifying them into families and predicting domains and important sites. They combine protein signatures from a number of member databases into a single searchable resource, capitalizing on their individual strengths to produce a powerful integrated database and diagnostic tool. This integrated database of predictive protein signatures is used for the classification and automatic annotation of proteins and genomes. InterPro classifies sequences at superfamily, family and subfamily levels, predicting the occurrence of functional domains, repeats and important sites. InterPro adds in-depth annotation, including GO terms, to the protein signatures. You can access the data programmatically, via Web Services. The member databases use a number of approaches: # ProDom: provider of sequence-clusters built from UniProtKB using PSI-BLAST. # PROSITE patterns: provider of simple regular expressions. # PROSITE and HAMAP profiles: provide sequence matrices. # PRINTS provider of fingerprints, which are groups of aligned, un-weighted Position Specific Sequence Matrices (PSSMs). # PANTHER, PIRSF, Pfam, SMART, TIGRFAMs, Gene3D and SUPERFAMILY: are providers of hidden Markov models (HMMs). Your contributions are welcome. You are encouraged to use the ''''Add your annotation'''' button on InterPro entry pages to suggest updated or improved annotation for individual InterPro entries.

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