BMRB Entry 52529

Title:
1H, 13C, and 15N chemical shift assignments for ubiquitin with K27M mutation
Deposition date:
2024-06-27
Original release date:
2024-06-28
Authors:
Gardiner, Colin; Wentz, Bryan; Fushman, David
Citation:

Citation: Gardiner, Colin; Wentz, Bryan; Fushman, David. "1H, 13C, and 15N chemical shift assignments for ubiquitin with K27M mutation"  Biomol. NMR Assignments ., .-..

Assembly members:

Assembly members:
entity_1, polymer, 76 residues, 8567.86 Da.

Natural source:

Natural source:   Common Name: Human   Taxonomy ID: 9606   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Homo sapiens

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET3a

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts212
15N chemical shifts72
1H chemical shifts407

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1K27M ubiquitin1

Entities:

Entity 1, K27M ubiquitin 76 residues - 8567.86 Da.

Ubiquitin with K27M mutation

1   METGLNILEPHEVALLYSTHRLEUTHRGLY
2   LYSTHRILETHRLEUGLUVALGLUPROSER
3   ASPTHRILEGLUASNVALMETALALYSILE
4   GLNASPLYSGLUGLYILEPROPROASPGLN
5   GLNARGLEUILEPHEALAGLYLYSGLNLEU
6   GLUASPGLYARGTHRLEUSERASPTYRASN
7   ILEGLNLYSGLUSERTHRLEUHISLEUVAL
8   LEUARGLEUARGGLYGLY

Samples:

sample_1: sodium phosphate 20 mM; DSS 100 uM; K27M Ubiquitin, [U-99% 13C; U-99% 15N], 300 uM

sample_2: sodium phosphate 20 mM; K27M Ubiquitin, [U-99% 15N], 1 mM; DSS 100 uM

sample_conditions_1: pH: 6.8; pressure: 1 atm; temperature: 300.5 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_2isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D HNCOsample_1isotropicsample_conditions_1
3D 1H-15N TOCSYsample_2isotropicsample_conditions_1
3D 1H-15N NOESYsample_2isotropicsample_conditions_1

Software:

NMRFAM-SPARKY v1.470 powered by Sparky 3.190 - chemical shift assignment, peak picking

TOPSPIN v4.07 - NMR data collection, processing of raw NMR data

NMR spectrometers:

  • Bruker AVANCE III 600 MHz

Related Database Links:

UNP P0CG47

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