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. 1999 Oct;10(10):3521–3538. doi: 10.1091/mbc.10.10.3521

Table 4.

Interactions of two-hybrid fusion proteins with Las17p and actin baits

GAL4-AD (activation domain) GAL4-BD (DNA binding domain) β-galactosidase activity (Miller units)
Las17p1–643 (pBMW172) Act1p1–375 (pDAB7)
Vector (pACTII) 00.1  ± 0.02 0.2  ± 0.06
Act1p−24–375 (pAIP70) 3.5  ± 0.5 1.4  ± 0.07
Arp2p1–391 (pAMW253) ≤0.1 ≤0.2
Arp3p1–448 (pAMW315) ≤0.1 ≤0.2
Las17p1–643 (pAMW173) 1.0  ± 0.1 1.2  ± 0.3
Act1p−28–375 (2×) 2.0  ± 0.1 1.1  ± 0.1
Rvs167p69–482 (2×) 50 ± 1 1.0  ± 0.1
Rvs167p191–482 (pAIP38) 54 ± 5 0.7  ± 0.2
Rvs167p239–482 (2×) 122 ± 3 ≤0.2
Rvs167p400–482 (2×) 16 ± 2 ≤0.2
Vrp1p492–818 (2×)* 62 ± 9 ≤0.2
Vrp1p783–818 (1×)* 29 ± 7 ≤0.2
Lsb1p8–241 (37×) 58 ± 5 ≤0.2
Lsb2p3–215 (9×) 96 ± 11 ≤0.2
Lsb3p186–451 (8×) 15 ± 4 ≤0.2
Ysc84p/Lsb4p270–468 (10×) 6 ± 0.2 ≤0.2
Lsb5p40–213 (11×) 34 ± 1 ≤0.2
Lsb6p67–607 (5×) 8 ± 1 ≤0.2

Vectors encoding fusions with the GAL4-(AD) were transformed into Y190 cells expressing GAL4-DB fusions with Las17p (pBMW172) or Act1p (pDAB7) and plated on SC − Trp and Leu plates. At least three colonies from each transformation were cultivated overnight in liquid selective medium (SC − Trp and Leu). β-Galactosidase activities were measured as described in MATERIALS AND METHODS. Values shown ± SD. Most double transformants that did not show blue color in the filter test were considered as approximately equal (≤) to background and were not assayed in liquid cultures. Plasmids marked with an asterisk were found in the FYRL genomic library; nonmarked entries are from the White cDNA library. Redundancy of the AD plasmids found is shown in parentheses. Not all candidates found are shown; interactions of the strongest and shortest fusions of each candidate are shown; longest fusions for Rvs167p and Vrp1p are also shown.