BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
Member of WWPDB

BMRB Entry 34018

Title: Lactococcin A immunity protein   PubMed: 27808503

Deposition date: 2016-07-01 Original release date: 2016-11-14

Authors: Persson, C.; Fuochi, V.; Pedersen, A.; Karlsson, B.; Nissen-Meyer, J.; Kristiansen, P.; Oppegard, C.

Citation: Kristiansen, P.; Persson, C.; Fuochi, V.; Pedersen, A.; Karlsson, G.; Nissen-Meyer, J.; Oppegard, C.. "Nuclear Magnetic Resonance Structure and Mutational Analysis of the Lactococcin A Immunity Protein."  Biochemistry 55, 6250-6257 (2016).

Assembly members:
entity_1, polymer, 117 residues, 13273.202 Da.

Natural source:   Common Name: Lactococcus lactis   Taxonomy ID: 1360   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Lactococcus lactis

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

Entity Sequences (FASTA):
entity_1: MSGSHHHHHHSSGIEGRGRM KKKQIEFENELRSMLATALE KDISQEERNALNIAEKALDN SEYLPKIILNLRKALTPLAI NRTLNHDLSELYKFITSSKA SNKNLGGGLIMSWGRLF

Data sets:
Data typeCount
13C chemical shifts394
15N chemical shifts98
1H chemical shifts590

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1entity_11

Entities:

Entity 1, entity_1 117 residues - 13273.202 Da.

1   METSERGLYSERHISHISHISHISHISHIS
2   SERSERGLYILEGLUGLYARGGLYARGMET
3   LYSLYSLYSGLNILEGLUPHEGLUASNGLU
4   LEUARGSERMETLEUALATHRALALEUGLU
5   LYSASPILESERGLNGLUGLUARGASNALA
6   LEUASNILEALAGLULYSALALEUASPASN
7   SERGLUTYRLEUPROLYSILEILELEUASN
8   LEUARGLYSALALEUTHRPROLEUALAILE
9   ASNARGTHRLEUASNHISASPLEUSERGLU
10   LEUTYRLYSPHEILETHRSERSERLYSALA
11   SERASNLYSASNLEUGLYGLYGLYLEUILE
12   METSERTRPGLYARGLEUPHE

Samples:

sample_1: lactococcin A immunity protein, [U-100% 13C; U-100% 15N], 0.5 mM

sample_conditions_1: ionic strength: 0.4 M; pH: 7.0; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
3D HNCOsample_1isotropicsample_conditions_1
3D HNCAsample_1isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D HN(CO)CAsample_1isotropicsample_conditions_1
3D HN(COCA)CBsample_1isotropicsample_conditions_1
3D HN(CA)COsample_1isotropicsample_conditions_1
3D 1H-15N NOESYsample_1isotropicsample_conditions_1
3D 1H-15N TOCSYsample_1isotropicsample_conditions_1
3D HCCH-TOCSYsample_1isotropicsample_conditions_1
3D 1H-13C NOESY aliphaticsample_1isotropicsample_conditions_1
3D 1H-13C NOESY aromaticsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-13C HSQC aliphaticsample_1isotropicsample_conditions_1
2D 1H-13C HSQC aromaticsample_1isotropicsample_conditions_1

Software:

Analysis, CCPN - chemical shift assignment

CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement

CYANA, Guntert, Mumenthaler and Wuthrich - structure calculation

NMR spectrometers:

  • Bruker AvanceIII 800 MHz

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