BMRB Entry 25240
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, SPARTA
BMRB Entry DOI: doi:10.13018/BMR25240
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Title: Solution structure of Twinstar from Drosophila melanogastor
Deposition date: 2014-09-20 Original release date: 2015-09-21
Authors: Shukla, Vaibhav; Maheshwari, Diva; Kumar, Dinesh; Arora, Ashish
Citation: Shukla, Vaibhav; Maheshwari, Diva; Jain, Anupam; Tripathi, Sarita; Kumar, Dinesh; Arora, Ashish. "Solution stucture and dynamics of Twinstar from Drosophila melanogastor" Not known ., .-..
Assembly members:
entity, polymer, 148 residues, 17180.645 Da.
Natural source: Common Name: fruit fly Taxonomy ID: 7227 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Drosophila melanogaster
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
entity: MASGVTVSDVCKTTYEEIKK
DKKHRYVIFYIRDEKQIDVE
TVADRNAEYDQFLEDIQKCG
PGECRYGLFDFEYMHQCQGT
SESSKKQKLFLMSWCPDTAK
VKKKMLYSSSFDALKKSLVG
VQKYIQATDLSEASREAVEE
KLRATDRQ
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 652 |
15N chemical shifts | 146 |
1H chemical shifts | 1008 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity | 1 |
Entities:
Entity 1, entity 148 residues - 17180.645 Da.
1 | MET | ALA | SER | GLY | VAL | THR | VAL | SER | ASP | VAL | ||||
2 | CYS | LYS | THR | THR | TYR | GLU | GLU | ILE | LYS | LYS | ||||
3 | ASP | LYS | LYS | HIS | ARG | TYR | VAL | ILE | PHE | TYR | ||||
4 | ILE | ARG | ASP | GLU | LYS | GLN | ILE | ASP | VAL | GLU | ||||
5 | THR | VAL | ALA | ASP | ARG | ASN | ALA | GLU | TYR | ASP | ||||
6 | GLN | PHE | LEU | GLU | ASP | ILE | GLN | LYS | CYS | GLY | ||||
7 | PRO | GLY | GLU | CYS | ARG | TYR | GLY | LEU | PHE | ASP | ||||
8 | PHE | GLU | TYR | MET | HIS | GLN | CYS | GLN | GLY | THR | ||||
9 | SER | GLU | SER | SER | LYS | LYS | GLN | LYS | LEU | PHE | ||||
10 | LEU | MET | SER | TRP | CYS | PRO | ASP | THR | ALA | LYS | ||||
11 | VAL | LYS | LYS | LYS | MET | LEU | TYR | SER | SER | SER | ||||
12 | PHE | ASP | ALA | LEU | LYS | LYS | SER | LEU | VAL | GLY | ||||
13 | VAL | GLN | LYS | TYR | ILE | GLN | ALA | THR | ASP | LEU | ||||
14 | SER | GLU | ALA | SER | ARG | GLU | ALA | VAL | GLU | GLU | ||||
15 | LYS | LEU | ARG | ALA | THR | ASP | ARG | GLN |
Samples:
sample_1: ammonium sulfate, [U-99% 15N], 0.1 % w/v; sodium phosphate 20 mM; sodium chloride 50 mM; DTT 1 mM; sodium azide 0.1 % w/v
sample_2: ammonium sulfate, [U-99% 15N], 0.1 % w/v; Glucose, [U-100% 13C], 0.2 % w/v; sodium phosphate 20 mM; sodium chloride 50 mM; sodium azide 0.1 % w/v; DTT 1 mM
sample_3: ammonium sulfate, [U-99% 15N], 0.1 % w/v; Glucose, [U-100% 13C], 0.2 % w/v; sodium phosphate 20 mM; sodium chloride 50 mM; sodium azide 0.1 % w/v; DTT 1 mM
sample_conditions_1: ionic strength: 50 mM; pH: 6.5; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
HNCANH | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_2 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_3 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aliphatic | sample_2 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aromatic | sample_3 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aliphatic | sample_3 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aromatic | sample_3 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
CBHD | sample_3 | isotropic | sample_conditions_1 |
CBHE | sample_3 | isotropic | sample_conditions_1 |
Software:
CARA, Keller and Wuthrich - chemical shift assignment
CYANA, Guntert, Mumenthaler and Wuthrich - structure solution
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
TOPSPIN, Bruker Biospin - processing
PSVS, Bhattacharya and Montelione - structure Validation
NMR spectrometers:
- Bruker Avance 800 MHz
Related Database Links:
PDB | |
GB | AAA19856 AAC46962 AAC46963 AAF47146 AAR09835 |
REF | NP_477034 XP_001360888 XP_001648106 XP_001648107 XP_001648108 |
SP | P45594 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts