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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR19732
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
All files associated with the entry
Citation: Gutte, Petrus; Jurt, Simon; Gruetter, Markus; Zerbe, Oliver. "The solution NMR structure of the NLRC5 caspase recruitment domain (CARD) reveals unusual structural features" Biochemistry 53, 3106-3117.
Assembly members:
entity, polymer, 101 residues, 11669.501 Da.
Natural source: Common Name: house mouse Taxonomy ID: 10090 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Mus musculus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pGEX-6p-1
Entity Sequences (FASTA):
entity: GPLGSMDAESIRLNNENLWA
WLVRLLSKNPEWLSAKLRSF
LPTMDLDCSYEPSNPEVIHR
QLNRLFAQGMATWKSFINDL
CFELDVPLDMEIPLVSIWGP
R
Data type | Count |
13C chemical shifts | 429 |
15N chemical shifts | 99 |
1H chemical shifts | 674 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | NLRC5_CARD | 1 |
Entity 1, NLRC5_CARD 101 residues - 11669.501 Da.
1 | GLY | PRO | LEU | GLY | SER | MET | ASP | ALA | GLU | SER | ||||
2 | ILE | ARG | LEU | ASN | ASN | GLU | ASN | LEU | TRP | ALA | ||||
3 | TRP | LEU | VAL | ARG | LEU | LEU | SER | LYS | ASN | PRO | ||||
4 | GLU | TRP | LEU | SER | ALA | LYS | LEU | ARG | SER | PHE | ||||
5 | LEU | PRO | THR | MET | ASP | LEU | ASP | CYS | SER | TYR | ||||
6 | GLU | PRO | SER | ASN | PRO | GLU | VAL | ILE | HIS | ARG | ||||
7 | GLN | LEU | ASN | ARG | LEU | PHE | ALA | GLN | GLY | MET | ||||
8 | ALA | THR | TRP | LYS | SER | PHE | ILE | ASN | ASP | LEU | ||||
9 | CYS | PHE | GLU | LEU | ASP | VAL | PRO | LEU | ASP | MET | ||||
10 | GLU | ILE | PRO | LEU | VAL | SER | ILE | TRP | GLY | PRO | ||||
11 | ARG |
sample_1: NLRC5_CARD, [U-100% 13C; U-100% 15N], 600 uM; MES 20 mM; sodium chloride 100 mM; potassium chloride 50 mM; TCEP 2 mM; H2O 95%; D2O, [U-100% 2H], 5%
sample_conditions_1: ionic strength: 0 M; pH: 6.2; pressure: 1 atm; temperature: 310 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aliphatic | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aromatic | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aliphatic | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aromatic | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
HB(CBCGCD)HD | sample_1 | isotropic | sample_conditions_1 |
TOPSPIN v2.1, Bruker Biospin - processing
CARA v1.8.6, Keller and Wuthrich - data analysis
UNIO v10, Torsten Herrmann - peak picking, structure solution
CYANA v2.1, Guntert, Mumenthaler and Wuthrich - structure solution
CHARMM, B. R. Brooks, C. L. Brooks III, D. M. York, and M. Karplus - refinement
UNP | C3VPR6 |
PDB | |
GB | ACP40992 |
REF | NP_001028379 XP_006531225 XP_006531226 XP_006531227 XP_006531228 |
SP | C3VPR6 |
AlphaFold | Q571H9 C3VPR6 |
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks