BMRB Entry 25656

Title:
NMR Assignments and structure of Translation initiation factor IF-1 from Burkholderia thailandensis E264.
Deposition date:
2015-06-09
Original release date:
2015-06-23
Authors:
Barnwal, Ravi Pratap; Varani, Gabriele
Citation:

Citation: Barnwal, Ravi Pratap; Varani, Gabriele. "NMR Assignments and structure of Translation initiation factor IF-1 from Burkholderia thailandensis E264."  To be Published ., .-..

Assembly members:

Assembly members:
entity, polymer, 72 residues, 8231.756 Da.

Natural source:

Natural source:   Common Name: Burkholderia thailandensis   Taxonomy ID: 57975   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Burkholderia thailandensis

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET28-AVA

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts281
15N chemical shifts71
1H chemical shifts368

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1Translation initiation factor IF-11

Entities:

Entity 1, Translation initiation factor IF-1 72 residues - 8231.756 Da.

1   METALALYSASPASPVALILEGLNMETGLN
2   GLYGLUVALILEGLUASNLEUPROASNALA
3   THRPHEARGVALLYSLEUGLUASNGLYHIS
4   VALVALLEUGLYHISILESERGLYLYSMET
5   ARGMETHISTYRILEARGILELEUPROGLY
6   ASPLYSVALTHRVALGLULEUTHRPROTYR
7   ASPLEUSERARGALAARGILEVALPHEARG
8   ALALYS

Samples:

sample_1: Translation initiation factor IF-1, [U-95% 13C; U-95% 15N], 1.2 mM

sample_conditions_1: pH: 6.0; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-13C HSQCsample_1isotropicsample_conditions_1
3D CBCA(CO)NHsample_1isotropicsample_conditions_1
3D HNCOsample_1isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D HBHA(CO)NHsample_1isotropicsample_conditions_1
3D HCCH-TOCSYsample_1isotropicsample_conditions_1
3D 1H-15N NOESYsample_1isotropicsample_conditions_1
3D 1H-13C NOESYsample_1isotropicsample_conditions_1

Software:

TOPSPIN, Bruker Biospin - collection, processing

CCPNMR, CCPN - chemical shift assignment, data analysis, peak picking

TALOS, Cornilescu, Delaglio and Bax - data analysis, structure solution

CYANA, Guntert, Mumenthaler and Wuthrich - geometry optimization, refinement, structure solution

NMR spectrometers:

  • Bruker Avance 600 MHz

Related Database Links:

PDB
DBJ BAG44869 BAO87561
EMBL CAD16707 CAH37203 CAR50566 CBJ36605 CBJ41758
GB AAU47849 ABA49847 ABB07070 ABC39541 ABD71909
REF WP_003264140 WP_003273618 WP_004185257 WP_004521905 WP_006577442
SP A0K3P6 A1V882 A2S7J7 A3MRX5 A3NEF8
AlphaFold A0K3P6 A1V882 A2S7J7 A3MRX5 A3NEF8

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