ABCC7 p.Tyr1219Phe
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PMID: 16966475
[PubMed]
Zhou Z et al: "The two ATP binding sites of cystic fibrosis transmembrane conductance regulator (CFTR) play distinct roles in gating kinetics and energetics."
No.
Sentence
Comment
106
The ATP dose-response relationships of Y1219F and Y1219I mutants lie between those of WT and Y1219G.
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ABCC7 p.Tyr1219Phe 16966475:106:39
status: NEW122 (A) Normalized ATP dose-response relationships of WT (black line, Michaelis-Menten fit from Fig. 1 D), Y1219W (brown), Y1219F (pink), Y1219I (blue), and Y1219G (green line, Michaelis-Menten fit from Fig. 1 D).
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ABCC7 p.Tyr1219Phe 16966475:122:119
status: NEW124 K1/2 values are 0.13 ± 0.02 mM (Y1219W), 0.46 ± 0.06 mM (Y1219F), and 0.94 ± 0.20 mM (Y1219I), respectively.
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ABCC7 p.Tyr1219Phe 16966475:124:67
status: NEW
PMID: 17700963
[PubMed]
Bompadre SG et al: "Cystic fibrosis transmembrane conductance regulator: a chloride channel gated by ATP binding and hydrolysis."
No.
Sentence
Comment
180
The mutation Y1219G shows an ATP dose-response relationship shifted more than 50-fold towards higher [ATP], however more conservative mutations (Y1219I, Y1219F) show smaller shifts, indicating the importance of the nature of the side chain in the interaction with the ATP molecule.
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ABCC7 p.Tyr1219Phe 17700963:180:153
status: NEW
PMID: 18391167
[PubMed]
Chen TY et al: "CLC-0 and CFTR: chloride channels evolved from transporters."
No.
Sentence
Comment
787
The ATP dose-response relationships of Y1219F and Y1219I mutants lie between those of wild type and Y1219G, suggesting a correlation between changes of the ATP sensitivity and the chemical natures of the side chain at this position.
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ABCC7 p.Tyr1219Phe 18391167:787:39
status: NEW
PMID: 20628841
[PubMed]
Shimizu H et al: "A stable ATP binding to the nucleotide binding domain is important for reliable gating cycle in an ABC transporter CFTR."
No.
Sentence
Comment
19
The degree of dose-response shift, a descending order of Y1218G, Y1219I, Y1219F and Y1219W, seemed to depend on the similarity of chemical properties, e.g., hydrophobicity and p bond by aromatic ring, of the side chains introduced by the mutations to tyrosine.
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ABCC7 p.Tyr1219Phe 20628841:19:73
status: NEW59 Figure 2b compares macroscopic current relaxations for Y1219G, Y1219I, Y1219F and Y1219W mutants.
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ABCC7 p.Tyr1219Phe 20628841:59:71
status: NEW61 The result with the Y1219F mutant lies c4; = 714 ms A B 2 s 0.4 pA ATP 5 mM ATP 5 mM 5 s 40 pA 1 s 20 pA Fig. 1 Macroscopic and microscopic currents of wild-type (WT)-CFTR.
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ABCC7 p.Tyr1219Phe 20628841:61:20
status: NEW67 The time constants of the initial fast phase for all the Y1219 mutants are within hundreds of milliseconds (sfast: 504 &#b1; 76 ms, n = 5 for Y1219G; 450 &#b1; 44 ms, n = 7 for Y1219I; 571 &#b1; 142 ms, n = 4 for Y1219F; 513 &#b1; 66 ms, n = 5 for Y1219W) and there is not significant difference in the fast time constant among these Y1219 mutants (Fig. 2b).
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ABCC7 p.Tyr1219Phe 20628841:67:213
status: NEW68 On the other hand, the time constants of the slow component for Y1219F and Y1219W are shorter than those of Y1219G and Y1219I (Fig. 3a).
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ABCC7 p.Tyr1219Phe 20628841:68:64
status: NEW69 More importantly, the fraction of the slow component (Fig. 3b) shows a gradual decrease as the mutation becomes less 'preserved` (Y1219G [ Y1219I [ Y1219F [ Y1219W).
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ABCC7 p.Tyr1219Phe 20628841:69:148
status: NEW70 It should be noted that, for technical reasons (detailed in ''Discussion``), our calculation of the fraction of the slow component is somewhat overestimated for Y1219F and Y1219W.
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ABCC7 p.Tyr1219Phe 20628841:70:161
status: NEW71 The actual values for Y1219F and Y1219W are lower than those shown in Fig. 3b.
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ABCC7 p.Tyr1219Phe 20628841:71:22
status: NEW76 The high affinity of P-ATP was suggested to come from its slow dissociation rate from NBD1 and NBD2 whereas the closing rate in P-ATP was just a little slower than that in B A C Y1219G ATP 5 mM 10 s 1 pA 25 s 2 pA Y1219G 25 s 2 pA ATP 5 mM W401G W 9 1 2 1 Y I 9 1 2 1 Y Y1219F 50 s 50 s 20 pA 50 s 20 pA 50 s 20 pA 20 pA ATP 5 mM 10 s 0.4 pA Y1219G Fig. 2 Macroscopic current relaxations for Y1219 and W401 mutants.
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ABCC7 p.Tyr1219Phe 20628841:76:270
status: NEW80 b Macroscopic current relaxations upon ATP wash-out for Y1219G, Y1219I, Y1219F and Y1219W.
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ABCC7 p.Tyr1219Phe 20628841:80:72
status: NEW82 The time constant and the fraction of the slow component are summarized in Fig. 3. c Single channel recording of Y1219G-CFTR showing a long opening even after ATP removal 35 30 25 20 15 10 5 0 Y1219G Y1219I Y1219F Y1219W 0.5 0.4 0.3 0.2 0.1 0.0 Y1219G Y1219I Y1219F Y1219W A slow / (A slow + A fast ) c4; slow (s) A B Fig. 3 Kinetic parameters of macroscopic current relaxations for Y1219G, Y1219I, Y1219F and Y1219W.
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ABCC7 p.Tyr1219Phe 20628841:82:207
status: NEWX
ABCC7 p.Tyr1219Phe 20628841:82:259
status: NEWX
ABCC7 p.Tyr1219Phe 20628841:82:402
status: NEW83 a Time constants of the slow component of the current relaxation for the Y1219 mutants. Y1219G: n = 5; Y1219I: n = 7; Y1219F: n = 4; and Y1219W: n = 5. b Fraction of the slow component (Aslow/Aslow ?
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ABCC7 p.Tyr1219Phe 20628841:83:118
status: NEW84 Afast) for the Y1219 mutants. Y1219G: n = 5; Y1219I: n = 7; Y1219F: n = 4; and Y1219W: n = 5 ATP because of their similar rate-limiting hydrolyzing rates [11].
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ABCC7 p.Tyr1219Phe 20628841:84:60
status: NEW132 Although the results with Y1219G and Y1219I mutations are quantified accurately, this may not be the case with the data for Y1219F and Y1219W.
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ABCC7 p.Tyr1219Phe 20628841:132:124
status: NEW162 If different mutations at Y1219 can affect the entry rate and the exit rate differently as shown in Table 2, this hypothesis may explain most of the results Table 1 Parameter sets (s-1 ) for the ''kiss and run`` hypothesis kCO1 kO1C kO1O2 kO2C Y1219G 3 or 0a 3 2 9 10-2 3.8 9 10-2 Y1219I : : 1.3 9 10-2 : Y1219F : : 1.1 9 10-2 : Y1219W : : 4 9 10-3 : a kCO1 was set to 3 s-1 for simulating the ''with ATP`` condition and 0 s-1 for simulating the ''after the ATP washout`` condition.
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ABCC7 p.Tyr1219Phe 20628841:162:305
status: NEW166 b Representative reproduced macroscopic current relaxations mimicking those in Y1219G (red), Y1219I (green), Y1219F (cyan) and Y1219W (blue).
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ABCC7 p.Tyr1219Phe 20628841:166:109
status: NEW
PMID: 25225552
[PubMed]
Lin WY et al: "A single amino acid substitution in CFTR converts ATP to an inhibitory ligand."
No.
Sentence
Comment
133
Y1219F, Y1219I, and Y1219G, mutations known to cause a graded change of the apparent affinity for Figure 3.ߓ Paradoxical [ATP] dependence of G551D-CFTR currents supports the hypothesis of two ATP-binding sites exerting opposite actions.
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ABCC7 p.Tyr1219Phe 25225552:133:0
status: NEW168 (A-C) Real-time current traces in response to ATP removal for G551D/Y1219F (A), G551D/Y1219I (B), and G551D/Y1219G (C).
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ABCC7 p.Tyr1219Phe 25225552:168:68
status: NEW