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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR17107
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
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Citation: Wan, Z.; Hua, Q.; Huang, K.; Hu, S.; Philips, N.; Whittaker, J.; Katsoyannis, P.; Weiss, M.. "Chiral Protein Engineering and its Application in G Health" J. Biol. Chem. ., .-..
Assembly members:
entity_1, polymer, 21 residues, 2383.700 Da.
Human Insulin, polymer, 30 residues, 3462.035 Da.
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: pBR322
Entity Sequences (FASTA):
entity_1: GIVEQCCTSICSLYQLENYC
N
Human Insulin: FVNQHLCGSHLVEALYLVCX
ERXFFYTKPT
Data type | Count |
1H chemical shifts | 345 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Human Insulin Mutant, 1 | 1 |
2 | Human Insulin Mutant, 2 | 2 |
Entity 1, Human Insulin Mutant, 1 21 residues - 2383.700 Da.
1 | GLY | ILE | VAL | GLU | GLN | CYS | CYS | THR | SER | ILE | ||||
2 | CYS | SER | LEU | TYR | GLN | LEU | GLU | ASN | TYR | CYS | ||||
3 | ASN |
Entity 2, Human Insulin Mutant, 2 30 residues - 3462.035 Da.
X = D-Alanine
1 | PHE | VAL | ASN | GLN | HIS | LEU | CYS | GLY | SER | HIS | |
2 | LEU | VAL | GLU | ALA | LEU | TYR | LEU | VAL | CYS | DAL | |
3 | GLU | ARG | DAL | PHE | PHE | TYR | THR | LYS | PRO | THR |
sample_1: entity_1 0.5 mM; D2O 10%; H2O 90%
sample_conditions_1: ionic strength: 0 mM; pH: 7.0; pressure: . mbar; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D TOCSY | sample_1 | isotropic | sample_conditions_1 |
NOESY | sample_1 | isotropic | sample_conditions_1 |
COSY | sample_1 | isotropic | sample_conditions_1 |
X-PLOR v3.5, Brunger - structure solution