Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR18693
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Citation: Taniguchi, Masahiro; Yoshinaga, Sosuke; Haga-Yamanaka, Sachiko; Touhara, Kazushige; Terasawa, Hiroaki. "Backbone and side-chain H, 15N and 13C assignments of mouse peptide ESP4." Biomol. NMR Assignments 8, 7-9 (2014).
PubMed: 23179060
Assembly members:
ESP4, polymer, 104 residues, Formula weight is not available
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: pET28A
Entity Sequences (FASTA):
ESP4: GSGRVLTQTGKETTMSADHK
TNHKADLEKNDSQGERNTQE
AFEMILCAFNQEKMLLKDQA
NSGQHELKLSKFFTALSKCG
AQNYQVDTVNYRIIPHIYPL
HSPK
Data type | Count |
13C chemical shifts | 410 |
15N chemical shifts | 100 |
1H chemical shifts | 645 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Exocrine gland-secreting peptide 4 | 1 |
Entity 1, Exocrine gland-secreting peptide 4 104 residues - Formula weight is not available
1 | GLY | SER | GLY | ARG | VAL | LEU | THR | GLN | THR | GLY | ||||
2 | LYS | GLU | THR | THR | MET | SER | ALA | ASP | HIS | LYS | ||||
3 | THR | ASN | HIS | LYS | ALA | ASP | LEU | GLU | LYS | ASN | ||||
4 | ASP | SER | GLN | GLY | GLU | ARG | ASN | THR | GLN | GLU | ||||
5 | ALA | PHE | GLU | MET | ILE | LEU | CYS | ALA | PHE | ASN | ||||
6 | GLN | GLU | LYS | MET | LEU | LEU | LYS | ASP | GLN | ALA | ||||
7 | ASN | SER | GLY | GLN | HIS | GLU | LEU | LYS | LEU | SER | ||||
8 | LYS | PHE | PHE | THR | ALA | LEU | SER | LYS | CYS | GLY | ||||
9 | ALA | GLN | ASN | TYR | GLN | VAL | ASP | THR | VAL | ASN | ||||
10 | TYR | ARG | ILE | ILE | PRO | HIS | ILE | TYR | PRO | LEU | ||||
11 | HIS | SER | PRO | LYS |
sample_1: ESP4, [U-100% 13C; U-100% 15N], 100 uM; H2O 90%; D2O 10%
sample_2: ESP4, [U-100% 15N], 100 uM; H2O 90%; D2O 10%
sample_3: ESP4, [U-100% 13C; U-100% 15N], 100 uM; D2O 100%
sample_conditions_1: pH: 3.5; pressure: 1 atm; temperature: 308.15 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_3 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aliphatic | sample_3 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_3 | isotropic | sample_conditions_1 |
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - collection, peak picking, processing
Olivia, Yokochi, Sekiguchi and Inagaki - chemical shift assignment, chemical shift calculation, data analysis
TOPSPIN, Bruker Biospin - collection, data analysis
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks