BMRB Entry 17473

Title:
Backbone 1H and 15N Chemical Shift Assignments for chimeric fusion of S. cerevisiae and C. albicans Sup35
Deposition date:
2011-02-16
Original release date:
2011-03-07
Authors:
Foo, Catherine; Kelly, Mark; Jonathan, Weissman
Citation:

Citation: Foo, Catherine; Ohhashi, Yumiko; Kelly, Mark; Tanaka, Motomasa; Weissman, Jonathan. "Radically different amyloid conformations dictate the seeding specificity of a chimeric sup35 prion."  J. Mol. Biol. 408, 1-8 (2011).
PubMed: 21333653

Assembly members:

Assembly members:
SC/CA_Sup35_chimera, polymer, 274 residues, Formula weight is not available

Natural source:

Natural source:   Common Name: yeast   Taxonomy ID: 4932   Superkingdom: Eukaryota   Kingdom: Fungi   Genus/species: Saccharomyces cerevisiae

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET29a Chim-His

Data sets:
Data typeCount
15N chemical shifts146
1H chemical shifts140

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
  • Hide all

Assembly:

Entity Assembly IDEntity NameEntity ID
1Chimera monomer1

Entities:

Entity 1, Chimera monomer 274 residues - Formula weight is not available

1   METSERASPSERASNGLNGLYASNASNGLN
2   GLNASNTYRGLNGLNTYRSERGLNASNGLY
3   ASNGLNGLNGLNGLYASNASNARGTYRGLN
4   GLYTYRGLNALATYRASNALAGLNALAGLN
5   SERPHEVALPROGLNGLYGLYTYRGLNGLN
6   PHEGLNGLNPHEGLNPROGLNGLNGLNGLN
7   GLNGLNTYRGLYGLYTYRASNGLNTYRASN
8   GLNTYRGLNGLYGLYTYRGLNGLNASNTYR
9   ASNASNARGGLYGLYTYRGLNGLNGLYTYR
10   ASNASNARGGLYGLYTYRGLNGLNASNTYR
11   ASNASNARGGLYGLYTYRGLNGLYTYRASN
12   GLNASNGLNGLNTYRGLYGLYTYRGLNGLN
13   TYRASNSERGLNPROGLNGLNGLNGLNGLN
14   GLNGLNSERGLNGLYMETSERLEUASNASP
15   PHEGLNLYSGLNGLNLYSGLNALAALAPRO
16   LYSPROLYSLYSTHRLEULYSLEUVALSER
17   SERSERGLYILELYSLEUALAASNALATHR
18   LYSLYSVALGLYTHRLYSPROALAGLUSER
19   ASPLYSLYSGLUGLUGLULYSSERALAGLU
20   THRLYSGLUPROTHRLYSGLUPROTHRLYS
21   VALGLUGLUPROVALLYSLYSGLUGLULYS
22   PROVALGLNTHRGLUGLULYSTHRGLUGLU
23   LYSSERGLULEUPROLYSVALGLUASPLEU
24   LYSILESERGLUSERTHRHISASNTHRASN
25   ASNALAASNVALTHRSERALAASPALALEU
26   ILELYSGLUGLNGLUGLUGLUVALASPASP
27   GLUVALVALASNASPHISHISHISHISHIS
28   HISHISHISHIS

Samples:

sample_1: SC/CA Sup35 chimera, [U-99% 13C; U-99% 15N], .135 nM; DMSO 100%

sample_conditions_1: pH: 5; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
3D HNCOsample_1isotropicsample_conditions_1
3D HNCAsample_1isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D CBCA(CO)NHsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
3D HN(CO)CAsample_1isotropicsample_conditions_1
3D HN(CA)NHsample_1isotropicsample_conditions_1

Software:

CcpNMR, CCPN - chemical shift assignment

NMR spectrometers:

  • Bruker Avance 800 MHz
  • Bruker DRX 500 MHz

Download HSQC peak lists in one of the following formats:
CSV: Backbone or all simulated peaks
SPARKY: Backbone or all simulated peaks