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 51600

Title: BIR2 domain of Xiap   PubMed: 37673444

Deposition date: 2022-08-29 Original release date: 2023-08-22

Authors: Favier, Adrien; Pellegrini, Erika

Citation: Lethier, Mathilde; Hons, Michael; Favier, Adrien; Brutscher, Bernhard; Boeri Erba, Elisabetta; Cusack, Stephen; Pellegrini, Erika. "Structure shows that the BIR2 domain of E3 ligase XIAP binds across the RIPK2 kinase dimer interface"  Life Sci. Alliance 6, e202201784-e202201784 (2023).

Assembly members:
entity_1, polymer, 117 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: pcDNA3

Entity Sequences (FASTA):
entity_1: RDHFALDRPSETHADYLLRT GQVVDISDTIYPRNPAMYSE EARLKSFQNWPDYAHLTPRE LASAGLYYTGIGDQVQCFAC GGKLKNWEPGDRAWSEHRRH FPNCFFVLGRNLNIRSE

Data sets:
Data typeCount
13C chemical shifts154
15N chemical shifts84
1H chemical shifts84

Additional metadata:

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

Entity Assembly IDEntity NameEntity ID
1Xiap-BIR21

Entities:

Entity 1, Xiap-BIR2 117 residues - Formula weight is not available

1   ARGASPHISPHEALALEUASPARGPROSER
2   GLUTHRHISALAASPTYRLEULEUARGTHR
3   GLYGLNVALVALASPILESERASPTHRILE
4   TYRPROARGASNPROALAMETTYRSERGLU
5   GLUALAARGLEULYSSERPHEGLNASNTRP
6   PROASPTYRALAHISLEUTHRPROARGGLU
7   LEUALASERALAGLYLEUTYRTYRTHRGLY
8   ILEGLYASPGLNVALGLNCYSPHEALACYS
9   GLYGLYLYSLEULYSASNTRPGLUPROGLY
10   ASPARGALATRPSERGLUHISARGARGHIS
11   PHEPROASNCYSPHEPHEVALLEUGLYARG
12   ASNLEUASNILEARGSERGLU

Samples:

sample_1: Xiap-BIR2, [U-100% 13C; U-100% 15N], 240 uM

sample_conditions_1: ionic strength: 0.15 M; pH: 7; pressure: 1 atm; temperature: 293.15 K

Experiments:

NameSampleSample stateSample conditions
3D BEST TROSY HNCAsample_1isotropicsample_conditions_1
3D BEST TROSY HNCACBsample_1isotropicsample_conditions_1
3D BEST TROSY HNCOCACBsample_1isotropicsample_conditions_1
3D BEST TROSY HNCOsample_1isotropicsample_conditions_1
3D BEST TROSY HNCOCAsample_1isotropicsample_conditions_1
2D 1H-15N BEST TROSYsample_1isotropicsample_conditions_1
3D 15N-separated NOESYsample_1isotropicsample_conditions_1

Software:

CcpNMR v3.0.4 - chemical shift assignment

NMR spectrometers:

  • Bruker AVANCE III 950 MHz

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