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 27598

Title: XRCC1-BRCT1   PubMed: 30650352

Deposition date: 2018-09-05 Original release date: 2019-02-07

Authors: Polo, Luis; Xu, Yingqi; Matthews, Steve; Oliver, Antony; Pearl, Laurence

Citation: Polo, Luis; Xu, Yingqi; Hornyak, Peter; Garces, Fernando; Zeng, Zhihong; Hailstone, Richard; Matthews, Steve; Caldecott, Keith; Oliver, Antony; Pearl, Laurence. "Efficient Single-Strand Break Repair Requires Binding to Both Poly(ADP-Ribose) and DNA by the Central BRCT Domain of XRCC1."  Cell Rep. 26, 573-581 (2019).

Assembly members:
XRCC1-BRCT1, polymer, 110 residues, Formula weight is not available

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

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET15b

Entity Sequences (FASTA):
XRCC1-BRCT1: GEGTEPRRPRAGPEELGKIL QGVVVVLSGFQNPFRSELRD KALELGAKYRPDWTRDSTHL ICAFANTPKYSQVLGLGGRI VRKEWVLDCHRMRRRLPSRR YLMAGPGSSS

Data sets:
Data typeCount
13C chemical shifts276
15N chemical shifts87
1H chemical shifts87

Additional metadata:

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

Entity Assembly IDEntity NameEntity ID
1XRCC1-BRCT11

Entities:

Entity 1, XRCC1-BRCT1 110 residues - Formula weight is not available

1   GLYGLUGLYTHRGLUPROARGARGPROARG
2   ALAGLYPROGLUGLULEUGLYLYSILELEU
3   GLNGLYVALVALVALVALLEUSERGLYPHE
4   GLNASNPROPHEARGSERGLULEUARGASP
5   LYSALALEUGLULEUGLYALALYSTYRARG
6   PROASPTRPTHRARGASPSERTHRHISLEU
7   ILECYSALAPHEALAASNTHRPROLYSTYR
8   SERGLNVALLEUGLYLEUGLYGLYARGILE
9   VALARGLYSGLUTRPVALLEUASPCYSHIS
10   ARGMETARGARGARGLEUPROSERARGARG
11   TYRLEUMETALAGLYPROGLYSERSERSER

Samples:

sample_1: XRCC1-BRCT1, [U-100% 13C; U-100% 15N], 0.3 mM; Tris-HCl 20 mM; NaCl 125 mM; TCEP 1 mM

sample_conditions_1: ionic strength: 145 mM; pH: 7.5; pressure: 1 atm; temperature: 303 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
3D CBCA(CO)NHsample_1isotropicsample_conditions_1
3D C(CO)NHsample_1isotropicsample_conditions_1

Software:

CCPNMR, CCPN - chemical shift assignment

NMR spectrometers:

  • Bruker DRX 600 MHz

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