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human prion protein mutant HuPrP(90-231, M129, V210I)
Authors
Biljan, I., Ilc, G., Giachin, G., Raspadori, A., Zhukov, I., Plavec, J., Legname, G.
Assembly
human prion protein mutant HuPrP(90-231, M129, V210I)
Entity
1. human prion protein mutant HuPrP(90-231, M129, V210I) (polymer, Thiol state: all disulfide bound), 147 monomers, 16633.37 Da Detail

GAMDPGQGGG THSQWNKPSK PKTNMKHMAG AAAAGAVVGG LGGYMLGSAM SRPIIHFGSD YEDRYYRENM HRYPNQVYYR PMDEYSNQNN FVHDCVNITI KQHTVTTTTK GENFTETDVK MMERVIEQMC ITQYERESQA YYQRGSS


Formula weight
16633.37 Da
Entity Connection
disulfide 1 Detail

IDTypeValue orderAtom ID 1Atom ID 2
1disulfidesing1:CYS95:SG1:CYS130:SG

Source organism
Homo sapiens
Exptl. method
solution NMR
Refine. method
molecular dynamics
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 97.3 %, Completeness: 86.7 %, Completeness (bb): 81.3 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All86.7 % (1452 of 1675)92.9 % (813 of 875)75.9 % (486 of 640)95.6 % (153 of 160)
Backbone81.3 % (707 of 870)94.4 % (286 of 303)66.9 % (285 of 426)96.5 % (136 of 141)
Sidechain92.8 % (870 of 937)92.1 % (527 of 572)94.2 % (326 of 346)89.5 % (17 of 19)
Aromatic87.0 % (134 of 154)87.0 % (67 of 77)86.8 % (66 of 76)100.0 % (1 of 1)
Methyl100.0 % (104 of 104)100.0 % (52 of 52)100.0 % (52 of 52)

1. HuPrP

GAMDPGQGGG THSQWNKPSK PKTNMKHMAG AAAAGAVVGG LGGYMLGSAM SRPIIHFGSD YEDRYYRENM HRYPNQVYYR PMDEYSNQNN FVHDCVNITI KQHTVTTTTK GENFTETDVK MMERVIEQMC ITQYERESQA YYQRGSS

Sample #1

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 5.5, Details 20 mM sodium acetic buffer, pH 5.5


#NameIsotope labelingTypeConcentration
1HuPrP[U-100% 13C; U-100% 15N]0.6 mM
2sodium acetatenatural abundance20 mM
3H2Onatural abundance90 %
4D2Onatural abundance10 %
Sample #2

Solvent system 100% D2O, Pressure 1 atm, Temperature 298 K, pH 5.5, Details 20 mM sodium acetic buffer, pD 5.9


#NameIsotope labelingTypeConcentration
5HuPrP[U-100% 13C; U-100% 15N]0.6 mM
6sodium acetatenatural abundance20 mM
7D2Onatural abundance100 %

LACS Plot; CA
Referencing offset: -0.02 ppm, Outliers: 1 Detail
LACS Plot; CB
Referencing offset: -0.02 ppm, Outliers: 1 Detail
LACS Plot; HA
Referencing offset: 0.06 ppm, Outliers: 1 Detail
Protein Blocks Logo
Calculated from 20 models in PDB: 2LEJ, Strand ID: A Detail


Release date
2011-08-18
Citation
Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation
Biljan, I., Ilc, G., Giachin, G., Raspadori, A., Zhukov, I., Plavec, J., Legname, G.
J. Mol. Biol. (2011), 412, 660-673, PubMed 21839748 , DOI 10.1016/j.jmb.2011.07.067 ,
Related entities 1. human prion protein mutant HuPrP(90-231, M129, V210I), : 1 : 1 : 99 entities Detail
Interaction partners 1. human prion protein mutant HuPrP(90-231, M129, V210I), : 73 interactors Detail
Experiments performed 11 experiments Detail
NMR combined restraints 4 contents Detail
Keywords human prion, pathologic mutant, point mutation