ABCMdb

ABCC7 p.Ser768Arg

None has been submitted yet.

Publications

PMID: 21059651 [PubMed] Wang G et al: "The inhibition mechanism of non-phosphorylated Ser768 in the regulatory domain of cystic fibrosis transmembrane conductance regulator."

No. Sentence Comment

7 More importantly, significant activation of a double mutant H950R/S768R needed only ATP. Login to comment
163 This notion was supported by the observation that S768R, a strong H-bond donor, failed to be activated by curcumin even in the presence of ATP (Fig. 6B). Login to comment
176 What is more, curcumin also activated H950R/ S768R and H950D/S768D constructs in the presence of ATP (Fig. 6E) because two strong proton donors or acceptors cannot form an H-bond (Table 1). Login to comment
178 Consistent with this notion, H950D/S768R was also not activated by curcumin with ATP (Fig. 6E). Login to comment
184 Fig. 7A shows that H950R/S768R was activated by ATP only, even without curcumin, but H950R or S768R was not (Fig. 7C). Login to comment
185 More importantly, H950R/S768R completely removed PKA dependence of channel activity (Fig. 7, A and D) no matter whether K978C, which promotes the channel opening without ATP, was inserted and accelerated channel activation by ATP (Fig. 7B) or not. Login to comment
191 Thus, a strong electrostatic expulsion between H950R/D and S768R/D promoted channel opening by ATP alone. Login to comment
193 Unlike H950R/S768R and H950D/S768D, which exerted an electrostatic interaction between the R domain and CL3, H950A, S768A, S768D, and H950R were not apparently activated by ATP only (Fig. 7C) but more sensitive to PKA than WT CFTR (Fig. 7D). Login to comment
213 Unlike H950A or S768A/D, an apparent open probability of H950R/S768R was higher (Po(app) ϭ 0.0042) than that of WT CFTR even in the absence of ATP, and ATP binding further increased channel opening (Po(app) ϭ 0.198) (Fig. 8, D and E). Login to comment
234 Error bars, S.E. TABLE 1 Potential roles in hydrogen bonding at the CL3-R domain interface Note that mutants whose channel activity was increased by curcumin in the presence of ATP are highlighted in boldface type. Residues Role in H-bond Mutants Arg Strong donor H950R, S768R, H950R/S768R, H950R/S768D, H950D/S768R Asp Strong acceptor H950D, S768D, H950D/S768D, H950R/S768D, H950D/S768R Thr, Gln, Ser, His Donor/Acceptor H950Q, S768T, WT Ala Negative control K946A, H950A, K951A, H954A, S955A, Q958A, S737A, S768A, ⌬R Inhibition of CFTR by Ser768 JANUARY 21, 2011•VOLUME 286•NUMBER 3 JOURNAL OF BIOLOGICAL CHEMISTRY 2177 matter whether cAMP was present or not in the extracellular perfusate. Login to comment
244 Although thiol-specific disulfide cross-linking of S768C to H950C or nearby cysteines inserted in CL3 inhibited channel activity primarily by stopping the channel from opening, an electrostatic expulsion between S768R/D and H950R/D clearly promoted channel opening even in the absence of ATP. Login to comment
248 Finally, both H950R and S768D promoted channel opening by ATP followed by curcumin or PKA phosphorylation, but H950D or S768R could not. Login to comment
255 PKA-dependent activity of His950 and Ser768 mutants with different H-bond donors and acceptors. A and B, activation of H950R/S768R (A) and H950R/S768R/K978C (B) before and after ATP (1. Login to comment
291 In agreement with a proposal of His950 as an H-bond acceptor and Ser768 as an H-bond donor, S768D and H950R mutants were more sensitive to ATP or curcumin or PKA phosphorylation than S768R and H950D (Figs. 6-8). Login to comment
305 Finally, both proton donors cannot form an inhibitory H-bond between H950R and S768R. Login to comment
306 Instead, an electrostatic expulsion between H950R and S768R dramatically increased the ATP-independent open probabilities and sensitivity to ATP and PKA (Figs. 7 and 8). Login to comment
343 It is expected that H950R and H950R/S768R may also exert similar effects on the basal channel opening. Login to comment