BMRB Entry 11321

Title:
Solution Structure of the IBR domain of the RING finger protein 31 protein
Deposition date:
2010-08-10
Original release date:
2011-08-19
Authors:
Miyamoto, K.; Koshiba, S.; Tomizawa, T.; Inoue, M.; Kigawa, T.; Yokoyama, S.
Citation:

Citation: Miyamoto, K.; Koshiba, S.; Tomizawa, T.; Inoue, M.; Kigawa, T.; Yokoyama, S.. "Solution Structure of the IBR domain of the RING finger protein 31 protein"  .

Assembly members:

Assembly members:
IBR domain, polymer, 86 residues, Formula weight is not available
ZN, non-polymer, 65.409 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: cell free synthesis   Host organism: E. coli - cell free   Vector: P040816-13

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts355
15N chemical shifts80
1H chemical shifts540

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1IBR domain1
2ZINC ION no.12
3ZINC ION no.22

Entities:

Entity 1, IBR domain 86 residues - Formula weight is not available

1   GLYSERSERGLYSERSERGLYALALEUPHE
2   HISLYSLYSLEUTHRGLUGLYVALLEUMET
3   ARGASPPROLYSPHELEUTRPCYSALAGLN
4   CYSSERPHEGLYPHEILETYRGLUARGGLU
5   GLNLEUGLUALATHRCYSPROGLNCYSHIS
6   GLNTHRPHECYSVALARGCYSLYSARGGLN
7   TRPGLUGLUGLNHISARGGLYARGSERCYS
8   GLUASPPHEGLNASNTRPLYSARGMETASN
9   SERGLYPROSERSERGLY

Entity 2, ZINC ION no.1 - Zn - 65.409 Da.

1   ZN

Samples:

sample_1: IBR domain, [U-13C; U-15N], 1.55 mM; d-Tris-HCl 20 mM; NaCl 200 mM; d-DTT 1 mM; NaN3 0.02%; ZnCl2 0.01 mM; H2O 90%; D2O 10%

condition_1: ionic strength: 220 mM; pH: 7.0; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
3D 15N-separated NOESYsample_1isotropiccondition_1
3D 13C-separated NOESYsample_1isotropiccondition_1

Software:

xwinnmr v3.5, Bruker - collection

NMRPipe v20031121, Delaglio, F. - processing

NMRView v5.0.4, Johnson, B. A. - data analysis

Kujira v0.925, Kobayashi, N. - data analysis

CYANA v2.0.17, Guntert, P. - refinement, structure solution

NMR spectrometers:

  • Bruker AVANCE 800 MHz

Related Database Links:

PDB
DBJ BAB15675 BAB70948 BAB84970 BAF35583 BAF83936
GB AAH09821 AAH12077 AAH17376 AAP12522 AIC60278
REF NP_001297261 NP_060469 XP_001112195 XP_001166671 XP_001490713
SP Q96EP0
AlphaFold Q96EP0

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