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 |