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 19832

Title: Structure of the antimicrobial peptide LsbB in DPC micelles   PubMed: 24993828

Deposition date: 2014-03-05 Original release date: 2014-07-14

Authors: Kristiansen, Per Eugen; Ovchinnikov, Kirill; Diep, Dzung Bao

Citation: Ovchinnikov, Kirill; Kristiansen, Per; Uzelac, Gordana; Topisirovic, Ljubisa; Kojic, Milan; Nissen-Meyer, Jon; Nes, Ingolf; Diep, Dzung. "Defining the Structure and Receptor Binding Domain of the Leaderless Bacteriocin LsbB."  J. Biol. Chem. 289, 23838-23845 (2014).

Assembly members:
Molecule_1, polymer, 30 residues, 3409.9902 Da.

Natural source:   Common Name: firmicutes   Taxonomy ID: 1358   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Lactococcus lactis

Experimental source:   Production method: chemical synthesis   Host organism: not applicable

Entity Sequences (FASTA):
Molecule_1: MKTILRFVAGYDIASHKKKT GGYPWERGKA

Data sets:
Data typeCount
13C chemical shifts98
15N chemical shifts28
1H chemical shifts230

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1antimicrobial peptide LsbB1

Entities:

Entity 1, antimicrobial peptide LsbB 30 residues - 3409.9902 Da.

1   METLYSTHRILELEUARGPHEVALALAGLY
2   TYRASPILEALASERHISLYSLYSLYSTHR
3   GLYGLYTYRPROTRPGLUARGGLYLYSALA

Samples:

sample_1: Molecule_1 1.0 ± 0.1 mM; DSS 0.2 ± 0.02 mM; DPC, [U-99% 2H], 200 ± 10 mM; H2O 95%; D2O 5%

sample_conditions_1: pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D DQF-COSYsample_1isotropicsample_conditions_1
2D 1H-1H TOCSYsample_1isotropicsample_conditions_1
2D 1H-13C HSQCsample_1isotropicsample_conditions_1
2D 1H-!H NOESYsample_1isotropicsample_conditions_1

Software:

CYANA, Guntert, Mumenthaler and Wuthrich - structure solution

SPARKY, Goddard - peak picking

TOPSPIN v2.4, Bruker Biospin - collection

CARA, Keller and Wuthrich - chemical shift assignment

TALOS v+, Cornilescu, Delaglio and Bax - data analysis

NMR spectrometers:

  • Bruker Avance 600 MHz

Related Database Links:

BMRB 19833
PDB
GB AAP73814 AGY45983
REF NP_861549 WP_011116717

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