Table S1. Summary and convergence of data obtained from the four technologies.
A. Protein purification
Step | Number |
Heterozygous diploid | 81 |
Haploid with tagged copy of gene as only copy of gene | 60 |
Tagged protein of expected size expressed in logarithmic cultures | 53 |
Tagged protein could be purified and analyzed by mass spectrometry | 47 |
Uncharacterized protein purified with other proteins | 37 |
Function could be predicted from copurifying proteins | 32 |
B. Two-hybrid analysis
Step | Number |
Two-hybrid baits constructed | 57 |
Two-hybrid array screens with unchracterized bait | 57 |
Two-hybrid array screens with positives | 43 |
Total two-hybrid positives from array screens | 271 |
C. Protein localization
Step | Number |
Heterozygous diploid | 89 |
Haploid with tagged copy of gene as only copy of gene | 76 |
Fluorescent fusion protein detected | 64 |
Localization1: | |
Nucleus | 32 |
Nucleolus | 13 |
Kinetochore | 2 |
Mitochondrion | 8 |
Nucleus and Mitochondrion | 2 |
Nuclear membrane | 2 |
Nuclear envelope and endoplasmic reticulum | 11 |
Golgi | 1 |
Plasma membrane | 1 |
Cytoplasm | 17 |
Vacuole | 1 |
D. Protein structure prediction
Step | Domains | ORFs |
PSI-blast | 40 | 29 |
Fold recognition | 34 | 28 |
Ab initio prediction | 51 | 19 |
Structures with significant match | 16 | 5 |
Structures w/o significant match | 38 | 14 |
Total | 133 | 76 |
E. Convergence of technologies
Number of Methods | Number of ORFs described |
1 | 19 |
2 | 21 |
3 | 33 |
4 | 23 |