Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR19240
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Citation: Mustafi, Sourajit; Chen, Hui; Li, Hongmin; Lemaster, David; Hernandez, Griselda. "Analyzing the visible conformational substates of the FK506-binding protein FKBP12." Biochem. J. 453, 371-380 (2013).
PubMed: 23688288
Assembly members:
FKBP12, polymer, 107 residues, 11819.5 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: pET11a
Entity Sequences (FASTA):
FKBP12: GVQVETISPGDGRTFPKRGQ
TCVVHYTGMLEDGKKFDSSR
DRNKPFKFMLGKQEVIRGWE
EGVAQMSVGQRAKLTISPDY
AYGATGHPGIIPPHATLVFD
VELLKLE
Data type | Count |
13C chemical shifts | 479 |
15N chemical shifts | 105 |
1H chemical shifts | 737 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | FKBP12 | 1 |
Entity 1, FKBP12 107 residues - 11819.5 Da.
1 | GLY | VAL | GLN | VAL | GLU | THR | ILE | SER | PRO | GLY | ||||
2 | ASP | GLY | ARG | THR | PHE | PRO | LYS | ARG | GLY | GLN | ||||
3 | THR | CYS | VAL | VAL | HIS | TYR | THR | GLY | MET | LEU | ||||
4 | GLU | ASP | GLY | LYS | LYS | PHE | ASP | SER | SER | ARG | ||||
5 | ASP | ARG | ASN | LYS | PRO | PHE | LYS | PHE | MET | LEU | ||||
6 | GLY | LYS | GLN | GLU | VAL | ILE | ARG | GLY | TRP | GLU | ||||
7 | GLU | GLY | VAL | ALA | GLN | MET | SER | VAL | GLY | GLN | ||||
8 | ARG | ALA | LYS | LEU | THR | ILE | SER | PRO | ASP | TYR | ||||
9 | ALA | TYR | GLY | ALA | THR | GLY | HIS | PRO | GLY | ILE | ||||
10 | ILE | PRO | PRO | HIS | ALA | THR | LEU | VAL | PHE | ASP | ||||
11 | VAL | GLU | LEU | LEU | LYS | LEU | GLU |
sample_1: FKBP12, [U-99% 13C; U-99% 15N], 1.5 mM; sodium phosphate 25 mM; DTT 2 mM; TCEP 2 mM; H2O 93%; D2O 7%
sample_2: FKBP12, [U-98% 15N], 1.5 mM; sodium phosphate 25 mM; DTT 2 mM; TCEP 2 mM; H2O 93%; D2O 7%
sample_conditions_1: ionic strength: 25 mM; pH: 6.50; pressure: 1 atm; temperature: 298.15 K
sample_condition_2: ionic strength: 25 mM; pH: 6.50; pressure: 1 atm; temperature: 298.15 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HCACO | sample_1 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aliphatic | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aromatic | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_2 | isotropic | sample_condition_2 |
2D DQF-COSY | sample_2 | isotropic | sample_condition_2 |
FELIX v2007, Accelrys Software Inc. - chemical shift assignment, peak picking, processing
BMRB | 16931 11471 16925 16931 16933 19241 |
PDB | |
DBJ | BAB22351 BAB27125 BAB31680 BAE32804 BAE40271 |
EMBL | CAA36462 CAA39272 CAA42762 CAG28541 CAG46965 |
GB | AAA19163 AAA31252 AAA35844 AAA58472 AAA58476 |
PRF | 1613455A |
REF | NP_000792 NP_001030533 NP_001033089 NP_001164597 NP_001239119 |
SP | P18203 P26883 P62942 P62943 Q62658 |
TPG | DAA23300 |
AlphaFold | P18203 P26883 P62942 P62943 Q62658 |
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