BMRB Entry 34576

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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR34576
MolProbity Validation Chart

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Title:
Solution structure of the Pax NRPS docking domain PaxB NDD
Deposition date:
2020-11-26
Original release date:
2021-06-02
Authors:
Watzel, J.; Sarawi, S.; Duchardt-Ferner, E.; Bode, H.; Woehnert, J.
Citation:

Citation: Watzel, J.; Sarawi, S.; Duchardt-Ferner, E.; Bode, H.; Woehnert, J.. "NMR resonance assignments for a docking domain pair with an attached thiolation domain from the PAX peptide-producing NRPS from Xenorhabdus cabanillasii."  Biomol. NMR Assign. 15, 229-234 (2021).
PubMed: 33675014

Assembly members:

Assembly members:
entity_1, polymer, 31 residues, 3616.222 Da.

Natural source:

Natural source:   Common Name: Xenorhabdus cabanillasii   Taxonomy ID: 1427517   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Xenorhabdus cabanillasii

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli BL21(DE3)   Vector: pET-11a

Entity Sequences (FASTA):

Entity Sequences (FASTA):
entity_1: MNNNELTSLPLAERKRLLEL AKAAKLSRQHY

Data sets:
Data typeCount
13C chemical shifts134
15N chemical shifts28
1H chemical shifts220

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
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Assembly:

Entity Assembly IDEntity NameEntity ID
1unit_11

Entities:

Entity 1, unit_1 31 residues - 3616.222 Da.

1   METASNASNASNGLULEUTHRSERLEUPRO
2   LEUALAGLUARGLYSARGLEULEUGLULEU
3   ALALYSALAALALYSLEUSERARGGLNHIS
4   TYR

Samples:

sample_1: PaxB NDD, [U-15N], 300 uM; sodium phosphate 50 mM; sodium chloride 100 mM; D2O, [U-2H], 5%; DSS 100 uM

sample_2: PaxB NDD, [U-15N], 300 uM; sodium phosphate 50 mM; sodium chloride 100 mM; D2O, [U-2H], 5%; DSS 100 uM

sample_3: PaxB NDD, [U-10% 13C; U-15N], 300 uM; sodium phosphate 50 mM; sodium chloride 100 mM; D2O, [U-2H], 5%; DSS 100 uM

sample_conditions_1: ionic strength: 100 mM; pH: 6.5; pressure: 1 atm; temperature: 293 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_2isotropicsample_conditions_1
3D HNCOsample_2isotropicsample_conditions_1
3D 1H-15N NOESYsample_1isotropicsample_conditions_1
3D 1H-13C NOESY aliphaticsample_2isotropicsample_conditions_1
2D 1H-13C HSQC aliphaticsample_3isotropicsample_conditions_1
3D HBHA(CO)NHsample_2isotropicsample_conditions_1
3D HNCACBsample_2isotropicsample_conditions_1
2D 1H-13C HSQC aliphaticsample_2isotropicsample_conditions_1
3D H(CCO)NHsample_2isotropicsample_conditions_1
3D C(CO)NHsample_2isotropicsample_conditions_1

Software:

TopSpin v3.6.2, Bruker Biospin - data analysis

CARA v1.8.4.2, Keller and Wuthrich - chemical shift assignment

CcpNmr Analysis v2.4.2, CCPN - peak picking

CYANA v3.98, Guntert, Mumenthaler and Wuthrich - structure calculation

OPALp, Koradi, Billeter and Guntert - refinement

NMR spectrometers:

  • Bruker AVANCE III HD 800 MHz
  • Bruker AVANCE II 600 MHz
  • Bruker AVANCE III HD 700 MHz

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