ABCC7 p.Thr757Ser
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PMID: 10692317
[PubMed]
Xie J et al: "Conformation, independent of charge, in the R domain affects cystic fibrosis transmembrane conductance regulator channel openings."
No.
Sentence
Comment
33
Site-specific mutations were constructed following the manufacturer`s instructions using the following three mutagenesis oligonucleotides (showed 5Ј to 3Ј, with mutated base underlined): P740A, G CTC AGA ATC TGC TAC TAA GGA CAG C (RsaI enzyme restriction site is destroyed); P750A, G GCT GAT GCG AGC CAG TAT CGC CTC (BsrI site is created); P759A/T757S, C CTG AAG CGT GGC CGG AGA GCT GAT (BsaHI site is created and BsrI site is destroyed).
X
ABCC7 p.Thr757Ser 10692317:33:358
status: NEW35 Although mutation was intended to affect only proline residues, upon sequencing, an additional conservative mutation, T757S, was noted.
X
ABCC7 p.Thr757Ser 10692317:35:118
status: NEW36 Subsequently, the individual prolines were mutated in sequence, with and without the T757S mutation, and their function was examined.
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ABCC7 p.Thr757Ser 10692317:36:85
status: NEWX
ABCC7 p.Thr757Ser 10692317:36:118
status: NEW37 No difference in channel activity was produced for any mutant by the T757S substitution.
X
ABCC7 p.Thr757Ser 10692317:37:69
status: NEWX
ABCC7 p.Thr757Ser 10692317:37:85
status: NEW38 Data presented in this paper for mutants containing P759A mutation are for constructs that also contain the unexpected T757S mutation.
X
ABCC7 p.Thr757Ser 10692317:38:69
status: NEWX
ABCC7 p.Thr757Ser 10692317:38:119
status: NEW34 Site-specific mutations were constructed following the manufacturer`s instructions using the following three mutagenesis oligonucleotides (showed 5b18; to 3b18;, with mutated base underlined): P740A, G CTC AGA ATC TGC TAC TAA GGA CAG C (RsaI enzyme restriction site is destroyed); P750A, G GCT GAT GCG AGC CAG TAT CGC CTC (BsrI site is created); P759A/T757S, C CTG AAG CGT GGC CGG AGA GCT GAT (BsaHI site is created and BsrI site is destroyed).
X
ABCC7 p.Thr757Ser 10692317:34:358
status: NEW39 Data presented in this paper for mutants containing P759A mutation are for constructs that also contain the unexpected T757S mutation.
X
ABCC7 p.Thr757Ser 10692317:39:119
status: NEW