BMRB Entry 25722

Title:
Unveiling the structural determinants of KIAA0323 binding preference for NEDD8
Deposition date:
2015-07-21
Original release date:
2016-07-25
Authors:
Santonico, Elena; Nepravishta, Ridvan; Mattioni, Anna; Valentini, Eleonora; Mandaliti, Walter; Procopio, Radha; Iannuccelli, Marta; Castagnoli, Luisa; Polo, Simona; Paci, Maurizio; Cesareni, Gianni
Citation:

Citation: Santonico, Elena; Nepravishta, Ridvan; Mattioni, Anna; Valentini, Eleonora; Mandaliti, Walter; Procopio, Radha; Iannuccelli, Marta; Castagnoli, Luisa; Polo, Simona; Paci, Maurizio; Cesareni, Gianni. "Unveiling the structural determinants of KIAA0323 binding preference for NEDD8."  .

Assembly members:

Assembly members:
KIAA0323, polymer, 52 residues, 6299.246 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: pGex6p1

Entity Sequences (FASTA):

Entity Sequences (FASTA):
KIAA0323: GGIRKTRETERLRRQLLEVF WGQDHKVDFILQREPYCRDI NQLSEALLSLNF

Data sets:
Data typeCount
15N chemical shifts50
1H chemical shifts181

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1KIAA03231

Entities:

Entity 1, KIAA0323 52 residues - 6299.246 Da.

The sequence is the C-terminal end of KIAA0323

1   GLYGLYILEARGLYSTHRARGGLUTHRGLU
2   ARGLEUARGARGGLNLEULEUGLUVALPHE
3   TRPGLYGLNASPHISLYSVALASPPHEILE
4   LEUGLNARGGLUPROTYRCYSARGASPILE
5   ASNGLNLEUSERGLUALALEULEUSERLEU
6   ASNPHE

Samples:

sample_1: KIAA0323, [U-100% 15N], 0.16 – 1.2 mM; H2O 90%; D2O 10%; Phosphate Buffer 12 mM

sample_conditions_1: ionic strength: 0.012 M; pH: 5.8; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-1H TOCSYsample_1isotropicsample_conditions_1
2D 1H-1H NOESYsample_1isotropicsample_conditions_1
3D 1H-15N NOESYsample_1isotropicsample_conditions_1
3D 1H-15N TOCSYsample_1isotropicsample_conditions_1

Software:

CNS, Brunger, Adams, Clore, Gros, Nilges and Read - geometry optimization, structure solution

NMR spectrometers:

  • Bruker Avance 700 MHz

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