Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR18610
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Citation: Vajpai, Navratna; Nisius, Lydia; Wiktor, Maciej; Grzesiek, Stephan. "High-pressure NMR reveals close similarity between cold and alcohol protein denaturation in ubiquitin." Proc. Natl. Acad. Sci. U.S.A. 110, .-. (2013).
PubMed: 23284170
Assembly members:
Ubiquitin, polymer, 76 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: pET-21b(+)
Entity Sequences (FASTA):
Ubiquitin: MQIFVKTLTGKTITLEVEPS
DTIENVKAKIQDKEGIPPDQ
QRLIFAGKQLEDGRTLSDYN
IQKESTLHLVLRLRGG
Data type | Count |
13C chemical shifts | 287 |
15N chemical shifts | 115 |
1H chemical shifts | 115 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Ubiquitin_folded | 1 |
2 | Ubiquitin_denatured | 1 |
Entity 1, Ubiquitin_folded 76 residues - Formula weight is not available
1 | MET | GLN | ILE | PHE | VAL | LYS | THR | LEU | THR | GLY | ||||
2 | LYS | THR | ILE | THR | LEU | GLU | VAL | GLU | PRO | SER | ||||
3 | ASP | THR | ILE | GLU | ASN | VAL | LYS | ALA | LYS | ILE | ||||
4 | GLN | ASP | LYS | GLU | GLY | ILE | PRO | PRO | ASP | GLN | ||||
5 | GLN | ARG | LEU | ILE | PHE | ALA | GLY | LYS | GLN | LEU | ||||
6 | GLU | ASP | GLY | ARG | THR | LEU | SER | ASP | TYR | ASN | ||||
7 | ILE | GLN | LYS | GLU | SER | THR | LEU | HIS | LEU | VAL | ||||
8 | LEU | ARG | LEU | ARG | GLY | GLY |
sample_1: Ubiquitin, [U-100% 13C; U-100% 15N], 1.0 mM; D2O, [U-2H], 10%; potassium phosphate 10 mM; sodium azide 0.02%; H2O 90%
sample_conditions_1: ionic strength: 10 mM; pH: 6.5; pressure: 2500 bar; temperature: 258 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRView, Johnson, One Moon Scientific - data analysis
PIPP, Garrett - peak picking
BMRB | 11505 11547 15047 15410 15689 15907 16228 16582 16626 16895 17181 17439 17769 17919 18582 18583 18584 18611 18737 19406 19412 25070 25123 25601 26604 4245 4375 |
PDB | |
DBJ | BAA03983 BAA09860 BAA11842 BAA11843 BAA23486 |
EMBL | CAA25706 CAA26488 CAA28495 CAA30183 CAA30815 |
GB | AAA02769 AAA28154 AAA28997 AAA28998 AAA28999 |
PIR | I50437 I51568 I65237 JN0790 S13928 |
PRF | 0412265A 1101405A 1212243A 1212243B 1212243C |
REF | NP_001005123 NP_001006688 NP_001009117 NP_001009202 NP_001009286 |
SP | P0C273 P0C275 P0C276 P0CG47 P0CG48 |
TPD | FAA00319 |
TPE | CEL68433 CEL70397 CEL75964 CEL78064 |
TPG | DAA18802 DAA20663 DAA20672 DAA24675 DAA28295 |
AlphaFold | P0C273 P0C275 P0C276 P0CG47 P0CG48 |
Download HSQC peak lists in one of the following formats:
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or all simulated peaks
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or all simulated peaks