PMID: 20004175

de Foresta B, Vincent M, Gallay J, Garrigos M
Interaction with membrane mimics of transmembrane fragments 16 and 17 from the human multidrug resistance ABC transporter 1 (hMRP1/ABCC1) and two of their tryptophan variants.
Biochim Biophys Acta. 2010 Mar;1798(3):401-14. Epub 2009 Dec 11., [PubMed]
Sentences
No. Mutations Sentence Comment
63 ABCC1 p.Cys1209Ser
X
ABCC1 p.Cys1209Ser 20004175:63:48
status: NEW
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ABCC1 p.Cys1205Ser
X
ABCC1 p.Cys1205Ser 20004175:63:33
status: NEW
view ABCC1 p.Cys1205Ser details
For this study, we synthesized a Cys1205Ser and Cys1209Ser double mutant of TM16 (mTM16), containing a single-Trp residue, W1198, close to the N-terminus (or W4 in the peptide sequence) (Table 1). Login to comment
65 ABCC1 p.Phe1213Trp
X
ABCC1 p.Phe1213Trp 20004175:65:77
status: NEW
view ABCC1 p.Phe1213Trp details
We synthesized a TM16 Trp variant (W19-mTM16), in which the aromatic residue Phe1213 was replaced by a tryptophan residue, to probe a part of TM16 closer to the C-terminus (i.e., to the extracellular side in the whole protein). Login to comment
67 ABCC1 p.Trp1246Tyr
X
ABCC1 p.Trp1246Tyr 20004175:67:116
status: NEW
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ABCC1 p.Ala1227Lys
X
ABCC1 p.Ala1227Lys 20004175:67:13
status: NEW
view ABCC1 p.Ala1227Lys details
ABCC1 p.Tyr1236Trp
X
ABCC1 p.Tyr1236Trp 20004175:67:101
status: NEW
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Similarly, a Ala1227Lys mutant of the TM17 fragment (mTM17) containing Trp1246 (or W20) [37] and the Tyr1236Trp and Trp1246Tyr variant of mTM17 (W10-mTM17), with its Trp closer to the extracellular side in the whole protein, were also synthesized (Table 1). Login to comment
346 ABCC1 p.Trp1246Tyr
X
ABCC1 p.Trp1246Tyr 20004175:346:75
status: NEW
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ABCC1 p.Tyr1236Trp
X
ABCC1 p.Tyr1236Trp 20004175:346:64
status: NEW
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For TM17, the Trp variant results from the two point mutations: Y1236W and W1246Y, so that the overall effect on ΔGu (interfacial partitioning free energy of the peptide) is null. Login to comment
348 ABCC1 p.Trp1198Tyr
X
ABCC1 p.Trp1198Tyr 20004175:348:70
status: NEW
view ABCC1 p.Trp1198Tyr details
For TM16, the variant results from the following two point mutations: W1198Y and F1113W. Login to comment