BMRB Entry 27351

Title:
Chemical shift assignments of the N-terminal peptide segment of human cystathionine-beta-synthase
Deposition date:
2018-01-03
Original release date:
2019-04-25
Authors:
Ohlenschlaeger, Oliver; Kumar, Amit; Ramachandran, Ramadurai
Citation:

Citation: Kumar, Amit; Wissbrock, Amelie; Goradia, Nishit; Bellstedt, Peter; Ramachandran, Ramadurai; Imhof, Diana; Ohlenschlaeger, Oliver. "Heme interaction of the intrinsically disordered N-terminal peptide segment of human cystathionine-beta-synthase"  Sci. Rep. 8, 2474-2474 (2018).
PubMed: 29410458

Assembly members:

Assembly members:
CBS40, polymer, 49 residues, 5210.65 Da.

Natural source:

Natural source:   Common Name: Human   Taxonomy ID: 9606   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Homo sapiens

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET-28a

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts178
15N chemical shifts42
1H chemical shifts167

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1CBS401

Entities:

Entity 1, CBS40 49 residues - 5210.65 Da.

Residues -8-0 (_Residue_author_seq_code) or 1-9 (_Residue_seq_code) represent a non-native cloning artefact.

1   GLUASNLEUTYRPHEGLNGLYVALASPMET
2   PROSERGLUTHRPROGLNALAGLUVALGLY
3   PROTHRGLYCYSPROHISARGSERGLYPRO
4   HISSERALALYSGLYSERLEUGLULYSGLY
5   SERPROGLUASPLYSGLUALALYSGLU

Samples:

sample_1: CBS40, [U-15N], 700 uM; sodium phosphate 20 mM; DTT 2 mM

sample_2: CBS40, [U-13C; U-15N], 700 uM; sodium phosphate 20 mM; DTT 2 mM

sample_conditions_1: ionic strength: 0.038 M; pH: 6.9; pressure: 1 atm; temperature: 283 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-13C HSQC aliphaticsample_2isotropicsample_conditions_1
3D HNCAsample_2isotropicsample_conditions_1
3D HN(CO)CAsample_2isotropicsample_conditions_1
3D HNCOsample_2isotropicsample_conditions_1
3D HNCACBsample_2isotropicsample_conditions_1
3D HBHANHsample_2isotropicsample_conditions_1
3D HNNsample_2isotropicsample_conditions_1

Software:

TOPSPIN v3.5, Bruker Biospin - collection

CCPN v2.4.2, CCPN - chemical shift assignment

NMR spectrometers:

  • Bruker Avance 600 MHz

Related Database Links:

UniProtKB P35520

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