Search

Mouse prion protein (121-231) with the mutations Y169A, Y225A, and Y226A.
Authors
Christen, B., Damberger, F.F., Perez, D.R., Hornemann, S., Wuthrich, K.
Assembly
Prion with Y169A, Y225A, Y226A mutation
Entity
1. Prion with Y169A, Y225A, Y226A mutation (polymer, Thiol state: all disulfide bound), 114 monomers, 13117.46 Da Detail

GSVVGGLGGY MLGSAMSRPM IHFGNDWEDR YYRENMYRYP NQVYYRPVDQ ASNQNNFVHD CVNITIKQHT VTTTTKGENF TETDVKMMER VVEQMCVTQY QKESQAAADG RRSS


Formula weight
13117.46 Da
Entity Connection
disulfide 1 Detail

IDTypeValue orderAtom ID 1Atom ID 2
1disulfidesing1:CYS61:SG1:CYS96:SG

Source organism
Mus musculus
Exptl. method
solution NMR
Refine. method
TORSION ANGLE DYNAMICS
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 100.0 %, Completeness: 89.2 %, Completeness (bb): 83.3 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All89.2 % (1169 of 1311)97.8 % (668 of 683)74.8 % (374 of 500)99.2 % (127 of 128)
Backbone83.3 % (565 of 678)95.7 % (224 of 234)69.4 % (231 of 333)99.1 % (110 of 111)
Sidechain95.9 % (708 of 738)98.9 % (444 of 449)90.8 % (247 of 272)100.0 % (17 of 17)
Aromatic79.7 % (94 of 118)98.3 % (58 of 59)60.3 % (35 of 58)100.0 % (1 of 1)
Methyl97.8 % (90 of 92)97.8 % (45 of 46)97.8 % (45 of 46)

1. Prion with Y169A, Y225A, Y226A mutation

GSVVGGLGGY MLGSAMSRPM IHFGNDWEDR YYRENMYRYP NQVYYRPVDQ ASNQNNFVHD CVNITIKQHT VTTTTKGENF TETDVKMMER VVEQMCVTQY QKESQAAADG RRSS

Sample

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 293.2 K, pH 4.5


#NameIsotope labelingTypeConcentration
1prion[U-99% 13C; U-99% 15N]1.4 mM
2sodium acetate[U-2H]10 mM
3sodium azidenatural abundance0.02 %
4H2Onatural abundance90 %
5D2Onatural abundance10 %

LACS Plot; CA
Referencing offset: 0.04 ppm, Outliers: 1 Detail
LACS Plot; CB
Referencing offset: 0.04 ppm, Outliers: 1 Detail
LACS Plot; HA
Referencing offset: 0.05 ppm, Outliers: 1 Detail
Protein Blocks Logo
Calculated from 20 models in PDB: 2L1K, Strand ID: A Detail


Release date
2012-08-01
Citation
Temperature-Induced Misfolding in Prion Protein: Evidence of Multiple Partially Disordered States Stabilized by Non-Native Hydrogen Bonds
Christen, B., Damberger, F.F., Perez, D.R., Hornemann, S., Wuthrich, K.
Biochemistry (2017), 56, 833-844, PubMed 28102071 , DOI 10.1021/acs.biochem.6b01042 ,
Related entities 1. Prion with Y169A, Y225A, Y226A mutation, : 1 : 13 : 142 entities Detail
Interaction partners 1. Prion with Y169A, Y225A, Y226A mutation, : 36 interactors Detail
Experiments performed 2 experiments Detail
nullKeywords mouse, mutation, NMR, prion, temperature