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Interactions of human retromer proteins with each other and SNX1 and SNX2. Full-length SNX1, SNX2, hVps26, hVps29, and hVps35 were fused to either the LexA DNA-binding domain in the pLexA vector or the B42 activation domain in the pB42AD vector as indicated. Interactions were assessed by using a liquid β-galactosidase assay and reported in Miller units (MU). Results are presented as mean ± SE of data obtained with 12–20 independent yeast clones.
