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Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the Phe508 region, the most common site of disease-causing DeltaF508 mutation -- P26
Authors
Massiah, M.A., Ko, Y.H., Pedersen, P.L., Mildvan, A.S.
Assembly
cystic fibrosis transmembrane conductance regulator (CFTR)
Entity
1. cystic fibrosis transmembrane conductance regulator (CFTR) (polymer, Thiol state: not present), 26 monomers, 3050.486 Da Detail

MPGTIKENII FGVSYDEYRY RSVIKA


Formula weight
3050.486 Da
Source organism
Homo sapiens
Exptl. method
NMR
Refine. method
DISTANCE GEOMETRY
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 100.0 %, Completeness: 85.5 %, Completeness (bb): 98.1 % Detail

Polymer type: polypeptide(L)

Total1H
All85.5 % (142 of 166)85.5 % (142 of 166)
Backbone98.1 % (52 of 53)98.1 % (52 of 53)
Sidechain79.6 % (90 of 113)79.6 % (90 of 113)
Aromatic82.4 % (14 of 17)82.4 % (14 of 17)
Methyl100.0 % (14 of 14)100.0 % (14 of 14)

1. PROTEIN (CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR))

MPGTIKENII FGVSYDEYRY RSVIKA

Sample

Pressure 1 atm, Temperature 298 K, pH 4.0


#NameIsotope labelingTypeConcentration
1PROTEIN (CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR))0.0 ~ 0.0 mM
2Trifluroethanol[U-2H]43 %

Protein Blocks Logo
Calculated from 13 models in PDB: 1CKX, Strand ID: A Detail


Release date
2000-12-03
Citation
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the Phe508 region, the most common site of disease-causing DeltaF508 mutation
Massiah, M.A., Ko, Y.H., Pedersen, P.L., Mildvan, A.S.
Biochemistry (1999), 38, 7453-7461, PubMed 10360942 , DOI 10.1021/bi9903603 ,
Related entities 1. cystic fibrosis transmembrane conductance regulator (CFTR), : 1 : 29 : 19 : 7 : 180 entities Detail
Interaction partners 1. cystic fibrosis transmembrane conductance regulator (CFTR), : 29 interactors Detail
Experiments performed 3 experiments Detail
nullKeywords P26 TFE, cystic fibrosis, peptides, NMR