ABCC1 p.Met443Leu

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PMID: 18775981 [PubMed] Grant CE et al: "Structural determinants of substrate specificity differences between human multidrug resistance protein (MRP) 1 (ABCC1) and MRP3 (ABCC3)."
No. Sentence Comment
143 The Y440F/I441L/M443L virtually eliminated LTC4 transport (Fig. 3B) but also reduced E217betaG transport by approximately 80% (Fig. 3C).
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ABCC1 p.Met443Leu 18775981:143:16
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144 Transport of LTC4, E217betaG, E13SO4, and MTX by Y440F, I441L, and M443L MRP1 Mutant Proteins.
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ABCC1 p.Met443Leu 18775981:144:67
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156 The Y440F and M443L mutations each independently decreased initial rates of LTC4 transport by approximately 60 and 50%, respectively, whereas the I441L mutation had little or no effect (Fig. 3B).
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ABCC1 p.Met443Leu 18775981:156:14
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157 In contrast, E217betaG transport was decreased approximately 50% by both the I441L and M443L mutations but only 20% by the Y440F mutation (Fig. 3C).
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ABCC1 p.Met443Leu 18775981:157:87
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158 All three mutations significantly decreased E13SO4 transport in the presence of 2 mM S-methyl GSH, with the Y440F, I441L, and M443L mutations reducing transport at 1 min by approximately 65, 50, and 90%, respectively (Fig. 3D).
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ABCC1 p.Met443Leu 18775981:158:126
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193 Mutations Included 23 M443L/Y440F/1441L 24 A481G/V482A/M483V/M485V 25 V479L/A481G/V482A/M483V/M485V 26 A493K/H494Q/S497L/N500S 27 V479L/A481G/V482A/M483V/M485V 28 V479L/A481G/V482A/M483V/N500S 29 A493K/H494Q/S497L/N500S/N506S 30 A493K/H494Q/S497L/N506S/T487M/K488R/T489A/Y490F consequence, it was technically impossible to determine an accurate Km for LTC4.
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ABCC1 p.Met443Leu 18775981:193:22
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235 The M443L mutation reduced S-methyl GSH-stimulated E13SO4 transport by 90% in Sf21 cells (Fig. 3D).
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ABCC1 p.Met443Leu 18775981:235:4
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237 Thus, the affinity for azidophenacyl-GSH is severely affected by the M443L mutation.
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ABCC1 p.Met443Leu 18775981:237:69
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242 Effect of the Y440F, I441L, M443L, and Y440F/I441L Mutations on Resistance to Vincristine, Doxorubicin, and VP-16.
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ABCC1 p.Met443Leu 18775981:242:28
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243 Lastly, the drug-resistance profiles of Y440F, I441L, M443L, and Y440F/I441L mutant proteins were examined because unlike MRP1, the profile of resistance to natural product drugs conferred by MRP3 is restricted primarily to epipodophyllotoxins (Deeley et al., 2006).
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ABCC1 p.Met443Leu 18775981:243:54
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295 In contrast to the Y440F mutation, the conservatively substituted I441L mutation had no effect on LTC4 or MTX transport but decreased transport of both E217betaG and E13SO4, whereas the M443L mutation decreased transport of all three conjugated substrates but not TABLE 2 Relative Drug Resistance of HEK293 Cells Transfected with Wild-Type and Mutant MRP1 Transfectant Drug (Relative Resistance Factora ) Vincristine VP-16 Doxorubicin HEKMRP1 15.6 Ϯ 2.5 16.2 Ϯ 4.9 4.5 Ϯ 0.3 HEKMRP1-Y440F 2.4 Ϯ 0.5 (5.1) 2.7 Ϯ 0.8 (6.0) 1.3 Ϯ 0.2 (1.9) HEKMRP1-1441L 8.9 Ϯ 2.5 (9.7) 4.1 Ϯ 1.2 (4.4) 3.7 Ϯ 1.4 (4.1) HEKMRP1-M443L 6.5 Ϯ 1.2 (6.0) 5.8 Ϯ 0.5 (5.4) 3.8 Ϯ 0.7 (3.6) HEKMRP1-Y440F/1441L 3.9 Ϯ 1.0 (7.5) 1.3 Ϯ 0.3 (1.7) 1.2 Ϯ 0.2 (1.5) HEKMRP3 1.1 Ϯ 0.1 6.4 Ϯ 1.9 0.87 Ϯ 0.2 a The relative resistance factor was obtained by dividing the IC50 values for the wild-type or mutant MRP1-transfected cells by the IC50 value for cells transfected with the expression vector alone.
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ABCC1 p.Met443Leu 18775981:295:186
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ABCC1 p.Met443Leu 18775981:295:661
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PMID: 21143116 [PubMed] He SM et al: "Structural and functional properties of human multidrug resistance protein 1 (MRP1/ABCC1)."
No. Sentence Comment
794 In addition, the Tyr440Phe, Ile441Leu, Met443Leu mutations decreased resistance to vincristine and etoposide 2-to 3-fold, whereas only the Tyr440Phe mutant displayed a major decrease in resistance to doxorubicin [374].
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ABCC1 p.Met443Leu 21143116:794:39
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