PMID: 21594796

Serohijos AW, Thibodeau PH, Dokholyan NV
Molecular modeling tools and approaches for CFTR and cystic fibrosis.
Methods Mol Biol. 2011;741:347-63., [PubMed]
Sentences
No. Mutations Sentence Comment
112 ABCC7 p.Phe508Ala
X
ABCC7 p.Phe508Ala 21594796:112:119
status: NEW
view ABCC7 p.Phe508Ala details
We used the following structures for wild type and mutant NBD1s: wild type (PDB ID: 2BBO), F508del (PDB ID: 1XMJ), and F508A (PDB ID: 1XMI) (see Note 2). Login to comment
113 ABCC7 p.Phe508Ala
X
ABCC7 p.Phe508Ala 21594796:113:4
status: NEW
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The F508A mutant has been shown to exhibit intermediate folding defects compared to F508del (7), and thus is an interesting control for the folding simulations. Login to comment
124 ABCC7 p.Phe508Ala
X
ABCC7 p.Phe508Ala 21594796:124:164
status: NEW
view ABCC7 p.Phe508Ala details
Simulation Protocol Using the simplified models described above, in our previous studies, we performed folding simulations for each NBD1-WT, NBD1-F508del, and NBD1-F508A. Login to comment
135 ABCC7 p.Phe508Ala
X
ABCC7 p.Phe508Ala 21594796:135:46
status: NEW
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(c) Contacts in NBD1-WT that perturbed in the F508A and F508del mutants. Login to comment
150 ABCC7 p.Phe508Ala
X
ABCC7 p.Phe508Ala 21594796:150:102
status: NEW
view ABCC7 p.Phe508Ala details
We found that at the given tmax, wild type exhibited higher folding probability than the F508del, and F508A folding probability is intermediate to that of wild type and F508del. Login to comment