ABCA1 p.Thr1305Ala

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PMID: 12869555 [PubMed] Martinez LO et al: "Phosphorylation of a pest sequence in ABCA1 promotes calpain degradation and is reversed by ApoA-I."
No. Sentence Comment
5 The ABCA1-T1286A/T1305A mutant was not degraded by calpain and was not further stabilized upon apoA-I treatment.
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ABCA1 p.Thr1305Ala 12869555:5:17
status: NEW
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6 The T1286A/T1305A mutant showed a 3.1-fold increase in cell surface expression and a 2.3-fold increase of apoAI-mediated cholesterol efflux compared with wild type ABCA1.
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ABCA1 p.Thr1305Ala 12869555:6:11
status: NEW
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31 mABCA1-FLAG mutation constructs were further called: MutAAAA for mutation to Ala on T1286A/S1296A/S1302A/T1305A, MutTAAT for mutation to Ala on S1296A/S1302A, and MutASSA for mutation to Ala on * This work was supported in part by National Institutes of Health Grant HL22682.
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ABCA1 p.Thr1305Ala 12869555:31:105
status: NEW
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41 Printed in U.S.A. This paper is available on line at http://www.jbc.org T1286A/T1305A.
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ABCA1 p.Thr1305Ala 12869555:41:81
status: NEW
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121 Mutation of Thr residues (1286 and 1305) decreases ABCA1 Phosphorylation. WT-mABCA1-FLAG, mABCA1delPEST-FLAG, mABCA1-FLAG mutated to Ala on T1286A/S1296A/S1302A/T1305A (MutAAAA), mutated to Ala on S1296A/S1302A (MutTAAT), or mutated to Ala on T1286A/T1305A (MutASSA), were transiently transfected in 6 wells of HEK-293 cells (2 ␮g of plasmid DNA per well).
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ABCA1 p.Thr1305Ala 12869555:121:161
status: NEW
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ABCA1 p.Thr1305Ala 12869555:121:250
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150 ABCA1 mutated on Thr-1286 and Thr-1305 is not degraded by calpain and is not stabilized by apoA-I. WT-mABCA1-FLAG or mABCA1-FLAG mutated to Ala on T1286A/T1305A (MutTSSA) were transiently transfected into HEK293 cells.
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ABCA1 p.Thr1305Ala 12869555:150:154
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189 Effect of apigenin (CK2 inhibitor) and H-89 (PKA inhibitor) on ABCA1 phosphorylation. WT-mABCA1-FLAG or mABCA1-FLAG mutated to Ala on T1286A/T1305A (MutASSA) were transiently transfected in 6 wells of HEK-293 cells (2 ␮g of plasmid DNA per well).
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ABCA1 p.Thr1305Ala 12869555:189:141
status: NEW
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30 mABCA1-FLAG mutation constructs were further called: MutAAAA for mutation to Ala on T1286A/S1296A/S1302A/T1305A, MutTAAT for mutation to Ala on S1296A/S1302A, and MutASSA for mutation to Ala on * This work was supported in part by National Institutes of Health Grant HL22682.
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ABCA1 p.Thr1305Ala 12869555:30:105
status: NEW
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38 39, Issue of September 26, pp. 37368-37374, 2003 (c) 2003 by The American Society for Biochemistry and Molecular Biology, Inc. Printed in U.S.A. This paper is available on line at http://www.jbc.org T1286A/T1305A.
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ABCA1 p.Thr1305Ala 12869555:38:208
status: NEW
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118 Mutation of Thr residues (1286 and 1305) decreases ABCA1 Phosphorylation. WT-mABCA1-FLAG, mABCA1delPEST-FLAG, mABCA1-FLAG mutated to Ala on T1286A/S1296A/S1302A/T1305A (MutAAAA), mutated to Ala on S1296A/S1302A (MutTAAT), or mutated to Ala on T1286A/T1305A (MutASSA), were transiently transfected in 6 wells of HEK-293 cells (2 òe;g of plasmid DNA per well).
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ABCA1 p.Thr1305Ala 12869555:118:161
status: NEW
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ABCA1 p.Thr1305Ala 12869555:118:250
status: NEW
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147 ABCA1 mutated on Thr-1286 and Thr-1305 is not degraded by calpain and is not stabilized by apoA-I. WT-mABCA1-FLAG or mABCA1-FLAG mutated to Ala on T1286A/T1305A (MutTSSA) were transiently transfected into HEK293 cells.
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ABCA1 p.Thr1305Ala 12869555:147:154
status: NEW
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186 Effect of apigenin (CK2 inhibitor) and H-89 (PKA inhibitor) on ABCA1 phosphorylation. WT-mABCA1-FLAG or mABCA1-FLAG mutated to Ala on T1286A/T1305A (MutASSA) were transiently transfected in 6 wells of HEK-293 cells (2 òe;g of plasmid DNA per well).
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ABCA1 p.Thr1305Ala 12869555:186:141
status: NEW
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