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. 2001 May 14;153(4):649–662. doi: 10.1083/jcb.153.4.649

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© 2001 The Rockefeller University Press

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

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The GAP1Δ2 truncation bypasses lst4Δ to restore Gap1p activity in the plasma membrane. (A) Wild-type (CKY482), lst4Δ (CKY702), and a bul1Δ bul2Δ (CKY701) strain were transformed with pGAP1 (pCK233) or pGAP1Δ2 (pCK234). Three transformants of each strain were cultured in minimal medium (SD Ammonia) at 24°C and assayed for [¹⁴C]citrulline uptake. Values are the mean and standard deviation for three transformants for each strain and are expressed as a percentage of the activity in wild-type (gap1Δ [pGAP1]).