Supplementary Materials for:
Protein Complex–Based Analysis Framework for High-Throughput
Data Sets
Arunachalam Vinayagam,* Yanhui Hu, Meghana Kulkarni, Charles Roesel, Richelle
Sopko, Stephanie E. Mohr, Norbert Perrimon*
*To whom correspondence should be addressed. E-mail: vinu{at}genetics.med.harvard.edu (A.V.);
perrimon{at}receptor.med.harvard.edu (N.P.)
This PDF file includes:
- Fig. S1. Schematic representation of protein complex scoring.
- Fig. S2. Snapshots of the COMPLEAT Web interface.
- Fig. S3. Complex enrichment results of baseline and EGF stimulus.
- Fig. S4. Baseline compared with EGF stimulus common complexes.
- Fig. S5. Baseline compared with EGF stimulus dynamic complexes: opposing
effects.
- Fig. S6. Baseline compared with EGF stimulus: baseline-specific dynamic
complexes.
- Fig. S7. Baseline compared with EGF stimulus: stimulus-specific dynamic
complexes.
- Fig. S8. Complex enrichment results of baseline and insulin stimulus.
- Fig. S9. Baseline compared with insulin stimulus: common complexes.
- Fig. S10. Baseline compared with insulin stimulus: baseline-specific dynamic
complexes.
- Fig. S11. Baseline compared with insulin stimulus: stimulus-specific dynamic
complexes.
- Table S1. Compilation of literature protein complexes for humans, Drosophila, and
yeast.
- Table S2. PPI data sets used to construct integrated PPI networks for humans,
Drosophila, and yeast.
- Table S3. Predicted protein complexes for humans, Drosophila, and yeast.
- Table S4. Redundancy in the protein complex resource.
- Table S5. Overlap of the literature and predicted complexes at the protein level.
- Table S6. Proteome covered by the protein complex resources.
- Table S7. Comparison of protein complexes with GO and KEGG with respect to co-citation.
- Table S8. Comparison of protein complexes with GO and KEGG with respect to
protein colocalization.
- Table S9. Comparison of protein complexes with GO and KEGG with respect to
gene coexpression.
- Table S10. Annotation of the protein complex resource.
- Table S11. Gene or protein input identifiers supported by the COMPLEAT.
- Table S20. Dynamic phosphosites changing in response to insulin treatment.
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Other Supplementary Material for this manuscript includes the following:
- Table S12 (Microsoft Excel format). Enriched protein complexes at baseline
(mtDER-S2R+ cell line).
- Table S13 (Microsoft Excel format). Enriched protein complexes at EGF stimulus
(mtDER-S2R+ cell line).
- Table S14 (Microsoft Excel format). Enriched protein complexes at baseline (S2R+
cell line).
- Table S15 (Microsoft Excel format). Enriched protein complexes at insulin stimulus
(S2R+ cell line).
- Table S16 (Microsoft Excel format). Consistent protein complexes with respect to
baseline versus EGF stimulus.
- Table S17 (Microsoft Excel format). Dynamic protein complexes with respect to
baseline versus EGF stimulus.
- Table S18 (Microsoft Excel format). Consistent protein complexes with respect to
baseline versus insulin stimulus.
- Table S19 (Microsoft Excel format). Dynamic protein complexes with respect to
baseline versus insulin stimulus.
[Download Tables S12-S19]
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Format: Zip Archive
Size: 314 KB
Citation: A. Vinayagam, Y. Hu, M. Kulkarni, C. Roesel, R. Sopko, S. E. Mohr,
N. Perrimon, Protein Complex–Based Analysis Framework for High-Throughput Data Sets.
Sci. Signal. 6, rs5 (2013).
© 2013 American Association for the Advancement of Science