BMRB Entry 16837
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR16837
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Title: HAV 3C C24S PubMed: 22156376
Deposition date: 2010-04-06 Original release date: 2011-12-15
Authors: Blaum, Baerbel; Winfried, Wuensche; Andrew, Benie
Citation: Blaum, Barbel; Wunsche, Winfried; Benie, Andrew; Kusov, Yuri; Peters, Hannelore; Gauss-Muller, Verena; Peters, Thomas; Sczakiel, Georg. "Functional binding of hexanucleotides to 3C protease of hepatitis A virus." Nucleic Acids Res. 40, 3042-3055 (2012).
Assembly members:
HAV_3C_protease_C24S, polymer, 217 residues, Formula weight is not available
Natural source: Common Name: Hepatitis A virus Taxonomy ID: 12092 Superkingdom: Virus Kingdom: not available Genus/species: Hepatovirus not available
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
HAV_3C_protease_C24S: STLEIAGLVRKNLVQFGVGE
KNGSVRWVMNALGVKDDWLL
VPSHAYKFEKDYEMMEFYFN
RGGTYYSISAGNVVIQSLDV
GFQDVVLMKVPTIPKFRDIT
QHFIKKGDVPRALNRLATLV
TTVNGTPMLISEGPLKMEEK
ATYVHKKNDGTTVDLTVDQA
WRGKGEGLPGMCGGALVSSN
QSIQNAILGIHVAGGNSILV
AKLVTQEMFQNIDKKIE
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 494 |
15N chemical shifts | 157 |
1H chemical shifts | 157 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | HAV 3C C24S | 1 |
Entities:
Entity 1, HAV 3C C24S 217 residues - Formula weight is not available
1 | SER | THR | LEU | GLU | ILE | ALA | GLY | LEU | VAL | ARG | ||||
2 | LYS | ASN | LEU | VAL | GLN | PHE | GLY | VAL | GLY | GLU | ||||
3 | LYS | ASN | GLY | SER | VAL | ARG | TRP | VAL | MET | ASN | ||||
4 | ALA | LEU | GLY | VAL | LYS | ASP | ASP | TRP | LEU | LEU | ||||
5 | VAL | PRO | SER | HIS | ALA | TYR | LYS | PHE | GLU | LYS | ||||
6 | ASP | TYR | GLU | MET | MET | GLU | PHE | TYR | PHE | ASN | ||||
7 | ARG | GLY | GLY | THR | TYR | TYR | SER | ILE | SER | ALA | ||||
8 | GLY | ASN | VAL | VAL | ILE | GLN | SER | LEU | ASP | VAL | ||||
9 | GLY | PHE | GLN | ASP | VAL | VAL | LEU | MET | LYS | VAL | ||||
10 | PRO | THR | ILE | PRO | LYS | PHE | ARG | ASP | ILE | THR | ||||
11 | GLN | HIS | PHE | ILE | LYS | LYS | GLY | ASP | VAL | PRO | ||||
12 | ARG | ALA | LEU | ASN | ARG | LEU | ALA | THR | LEU | VAL | ||||
13 | THR | THR | VAL | ASN | GLY | THR | PRO | MET | LEU | ILE | ||||
14 | SER | GLU | GLY | PRO | LEU | LYS | MET | GLU | GLU | LYS | ||||
15 | ALA | THR | TYR | VAL | HIS | LYS | LYS | ASN | ASP | GLY | ||||
16 | THR | THR | VAL | ASP | LEU | THR | VAL | ASP | GLN | ALA | ||||
17 | TRP | ARG | GLY | LYS | GLY | GLU | GLY | LEU | PRO | GLY | ||||
18 | MET | CYS | GLY | GLY | ALA | LEU | VAL | SER | SER | ASN | ||||
19 | GLN | SER | ILE | GLN | ASN | ALA | ILE | LEU | GLY | ILE | ||||
20 | HIS | VAL | ALA | GLY | GLY | ASN | SER | ILE | LEU | VAL | ||||
21 | ALA | LYS | LEU | VAL | THR | GLN | GLU | MET | PHE | GLN | ||||
22 | ASN | ILE | ASP | LYS | LYS | ILE | GLU |
Samples:
sample_1: HAV 3C protease C24S, [U-100% 13C; U-100% 15N; U-75% 2H], 0.2 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 200 mM; pH: 7.4; pressure: 1 atm; temperature: 303 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CACB | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
SPARKY, Goddard - chemical shift assignment
NMR spectrometers:
- Bruker Avance 700 MHz
Related Database Links:
PDB | |
DBJ | BAA35102 BAA35103 BAA35104 BAA35105 BAA35106 |
EMBL | CAA33491 CAA50195 CAA53024 CAA53025 CAA53026 |
GB | AAA45465 AAA45466 AAA45467 AAA45468 AAA45469 |
PIR | GNNYHB |
REF | NP_041007 NP_041008 NP_740558 |
SP | A3FMB2 A5LGW7 P06441 P08617 P13901 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts