BMRB Entry 11019

Title:
Cox17
Deposition date:
2007-12-10
Original release date:
2008-06-27
Authors:
Banci, Lucia; Bertini, Ivano; Ciofi-Baffoni, Simone; Janicka, Anna; Martinelli, Manuele; Kozlowski, Henryk; Palumaa, Peep
Citation:

Citation: Banci, Lucia; Bertini, Ivano; Ciofi Baffoni, Simone; Janicka, Anna; Martinelli, Manuele; Kozlowski, Henryk; Palumaa, Peep. "A structural-dynamical characterization of human Cox17"  J. Biol. Chem. 283, 7912-7920 (2008).
PubMed: 18093982

Assembly members:

Assembly members:
Cox17, polymer, 67 residues, 7307.5 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: pETG-30A

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts251
15N chemical shifts62
1H chemical shifts413

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1Cox17 monomer1

Entities:

Entity 1, Cox17 monomer 67 residues - 7307.5 Da.

Cox17 protein contains four additional amino acids (GSFT) at the N-terminus, corresponding to the TEV protease recognition site.

1   GLYSERPHETHRMETPROGLYLEUVALASP
2   SERASNPROALAPROPROGLUSERGLNGLU
3   LYSLYSPROLEULYSPROCYSCYSALACYS
4   PROGLUTHRLYSLYSALAARGASPALACYS
5   ILEILEGLULYSGLYGLUGLUHISCYSGLY
6   HISLEUILEGLUALAHISLYSGLUCYSMET
7   ARGALALEUGLYPHELYSILE

Samples:

sample_1: Cox170.5 – 1 mM; DTT 1 mM; potassium phosphate 50 mM; H2O 90%; D2O 10%

sample_2: Cox17, [U-100% 15N], 0.5 – 1 mM; DTT 1 mM; potassium phosphate 50 mM; H2O 90%; D2O 10%

sample_3: Cox17, [U-100% 13C; U-100% 15N], 0.5 – 1 mM; DTT 1 mM; potassium phosphate 50 mM; H2O 90%; D2O 10%

sample_conditions_1: ionic strength: 50 mM; pH: 7.2; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_2isotropicsample_conditions_1
3D CBCA(CO)NHsample_3isotropicsample_conditions_1
3D HNCACBsample_3isotropicsample_conditions_1
3D HNCAsample_3isotropicsample_conditions_1
3D HNCOsample_3isotropicsample_conditions_1
3D HN(CO)CAsample_3isotropicsample_conditions_1
3D HBHA(CO)NHsample_3isotropicsample_conditions_1
3D HCCH-TOCSYsample_3isotropicsample_conditions_1
2D 1H-1H NOESYsample_1isotropicsample_conditions_1
3D 1H-15N NOESYsample_2isotropicsample_conditions_1
3D 1H-13C NOESYsample_3isotropicsample_conditions_1
2D 1H-1H TOCSYsample_1isotropicsample_conditions_1
3D HNHAsample_2isotropicsample_conditions_1
3D HN(CA)COsample_3isotropicsample_conditions_1

Software:

AMBER v8.0, Case, Darden, Cheatham, III, Simmerling, Wang, Duke, Luo, ... and Koll - refinement

TOPSPIN, Bruker Biospin - collection

CYANA v2.1, Guntert, Mumenthaler and Wuthrich - structure solution

ATNOS, Herrmann, Guntert, Wuthrich - peak picking

CANDID, Herrmann, Guntert, Wuthrich - NOEs assignment

CARA, Keller - data analysis

NMR spectrometers:

  • Bruker AVANCE 900 MHz
  • Bruker AVANCE 500 MHz
  • Bruker AVANCE 700 MHz

Related Database Links:

BMRB 11020 17821
PDB
DBJ BAG35079
GB AAA98114 AAF82569 AAH10933 AAI05281 AAI08318
REF NP_001239469 NP_001254468 NP_005685 XP_002758821 XP_003261908
SP Q14061
AlphaFold Q14061

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