ABCB1 p.Glu1013Ala
| Predicted by SNAP2: | A: N (53%), C: D (53%), D: N (97%), F: D (66%), G: D (66%), H: D (53%), I: D (66%), K: N (57%), L: D (63%), M: D (63%), N: N (87%), P: D (80%), Q: N (53%), R: N (61%), S: N (66%), T: D (59%), V: D (63%), W: D (71%), Y: D (66%), |
| Predicted by PROVEAN: | A: D, C: D, D: N, F: D, G: D, H: D, I: D, K: D, L: D, M: D, N: D, P: D, Q: N, R: D, S: D, T: D, V: D, W: D, Y: D, |
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[hide] The multidrug transporter Pdr5 on the 25th anniver... Biochem J. 2015 May 1;467(3):353-63. doi: 10.1042/BJ20150042. Golin J, Ambudkar SV
The multidrug transporter Pdr5 on the 25th anniversary of its discovery: an important model for the study of asymmetric ABC transporters.
Biochem J. 2015 May 1;467(3):353-63. doi: 10.1042/BJ20150042., [PMID:25886173]
Abstract [show]
Asymmetric ABC (ATP-binding cassette) transporters make up a significant proportion of this important superfamily of integral membrane proteins. These proteins contain one canonical (catalytic) ATP-binding site and a second atypical site with little enzymatic capability. The baker's yeast (Saccharomyces cerevisiae) Pdr5 multidrug transporter is the founding member of the Pdr subfamily of asymmetric ABC transporters, which exist only in fungi and slime moulds. Because these organisms are of considerable medical and agricultural significance, Pdr5 has been studied extensively, as has its medically important homologue Cdr1 from Candida albicans. Genetic and biochemical analyses of Pdr5 have contributed important observations that are likely to be applicable to mammalian asymmetric ABC multidrug transporter proteins, including the basis of transporter promiscuity, the function of the non-catalytic deviant ATP-binding site, the most complete description of an in vivo transmission interface, and the recent discovery that Pdr5 is a molecular diode (one-way gate). In the present review, we discuss the observations made with Pdr5 and compare them with findings from clinically important asymmetric ABC transporters, such as CFTR (cystic fibrosis transmembrane conductance regulator), Cdr1 and Tap1/Tap2.
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No. Sentence Comment
287 Gupta et al. [24] demonstrated further that replacement of multiple (Walker A, Walker B, and C-loop) deviant motifs with canonical ones in Pdr5 caused a significant loss, but not a complete elimination, of both ATPase and transport functions, rather reminiscent of the E1013A and D1042E phenotypes seen by Furman et al. [23].
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ABCB1 p.Glu1013Ala 25886173:287:269
status: NEW