BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
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BMRB Entry 18141

Title: Solution NMR structure of the novel conotoxin im23a from Conus imperialis   PubMed: 22399292

Deposition date: 2011-12-15 Original release date: 2012-03-19

Authors: Khoo, Keith; Galea, Charles; Boonyalai, Nonlawat; Norton, Raymond

Citation: Ye, Mingyu; Khoo, Keith; Xu, Shaoqiong; Zhou, Mi; Boonyalai, Nonlawat; Perugini, Matthew; Shao, Xiaoxia; Chi, Chengwu; Galea, Charles; Wang, Chunguang; Norton, Raymond. "A Helical Conotoxin from Conus imperialis Has a Novel Cysteine Framework and Defines a New Superfamily."  J. Biol. Chem. 287, 14973-14983 (2012).

Assembly members:
entity, polymer, 42 residues, 4834.591 Da.

Natural source:   Common Name: Conus imperialis   Taxonomy ID: 35631   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Conus imperialis

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

Entity Sequences (FASTA):
entity: IPYCGQTGAECYSWCIKQDL SKDWCCDFVKDIRMNPPADK CP

Data sets:
Data typeCount
13C chemical shifts29
15N chemical shifts43
1H chemical shifts281

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1novel conotoxin im23a1

Entities:

Entity 1, novel conotoxin im23a 42 residues - 4834.591 Da.

1   ILEPROTYRCYSGLYGLNTHRGLYALAGLU
2   CYSTYRSERTRPCYSILELYSGLNASPLEU
3   SERLYSASPTRPCYSCYSASPPHEVALLYS
4   ASPILEARGMETASNPROPROALAASPLYS
5   CYSPRO

Samples:

GS-15N-im23a-recombinant: entity, [U-15N], 128 uM; H2O 95%; D2O 5%

GS-im23a-recombinant-unlabelled: entity 128 uM; H2O 95%; D2O 5%

sample_conditions_1: pH: 5.6; pressure: 1 atm; temperature: 273 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCGS-15N-im23a-recombinantisotropicsample_conditions_1
2D 1H-13C HSQCGS-15N-im23a-recombinantisotropicsample_conditions_1
2D 1H-1H TOCSYGS-15N-im23a-recombinantisotropicsample_conditions_1
2D DQF-COSYGS-15N-im23a-recombinantisotropicsample_conditions_1
2D 1H-1H NOESYGS-15N-im23a-recombinantisotropicsample_conditions_1
3D 1H-15N NOESYGS-15N-im23a-recombinantisotropicsample_conditions_1
2D 1H-1H TOCSYGS-im23a-recombinant-unlabelledisotropicsample_conditions_1
2D 1H-1H NOESYGS-im23a-recombinant-unlabelledisotropicsample_conditions_1

Software:

TOPSPIN, Bruker Biospin - collection, data analysis

XEASY, Bartels et al. - chemical shift assignment, peak picking, processing

X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution

NMR spectrometers:

  • Bruker DRX 600 MHz
  • Bruker Avance 800 MHz
  • Bruker Avance 500 MHz

Related Database Links:

PDB
GB ACQ65998 AFE82855
SP D0PX84

Download simulated HSQC data in one of the following formats:
CSV: Backbone or all simulated shifts
SPARKY: Backbone or all simulated shifts