BMRB Entry 30638
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR30638
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Title: Structural Basis for Client Recognition and Activity of Hsp40 Chaperones
Deposition date: 2019-07-12 Original release date: 2019-09-11
Authors: Jiang, Y.; Rossi, P.; Kalodimos, C.
Citation: Jiang, Y.; Rossi, P.; Kalodimos, C.. "Structural Basis for Client Recognition and Activity of Hsp40 Chaperones" . ., .-..
Assembly members:
entity_1, polymer, 280 residues, 31023.424 Da.
entity_2, polymer, 471 residues, 49492.367 Da.
Natural source: Common Name: Thermus thermophilus Taxonomy ID: 300852 Superkingdom: Bacteria Kingdom: not available Genus/species: Thermus thermophilus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli BL21(DE3)
Entity Sequences (FASTA):
entity_1: MAAKKDYYAILGVPRNATQE
EIKRAYKRLARQYHPDVNKS
PEAEEKFKEINEAYAVLSDP
EKRRIYDTYGTTEAPPPPPP
GGYDFSGFDVEDFSEFFQEL
FGPGLFGGFGRRSRKGRDLR
AELPLTLEEAFHGGERVVEV
AGRRVSVRIPPGVREGSVIR
VPGMGGQGNPPGDLLLVVRL
LPHPVFRLEGQDLYATLDVP
APIAVVGGKVRAMTLEGPVE
VAVPPRTQAGRKLRLKGKGF
PGPAGRGDLYLEVRITIPER
LTPEEEALWKKLAEAYYARA
entity_2: MKQSTIALALLPLLFTPVTK
ARTPEMPVLENRAAQGDITA
PGGARRLTGDQTAALRDSLS
DKPAKNIILLIGDGMGDSEI
TAARNYAEGAGGFFKGIDAL
PLTGQYTHYALNKKTGKPDY
VTDSAASATAWSTGVKTYNG
ALGVDIHEKDHPTILEMAKA
AGLATGNVSTAELQDATPAA
LVAHVTSRKCYGPSATSEKC
PGNALEKGGKGSITEQLLNA
RADVTLGGGAKTFAETATAG
EWQGKTLREQAQARGYQLVS
DAASLNSVTEANQQKPLLGL
FADGNMPVRWLGPKATYHGN
IDKPAVTCTPNPQRNDSVPT
LAQMTDKAIELLSKNEKGFF
LQVEGASIDKQDHAANPCGQ
IGETVDLDEAVQRALEFAKK
EGNTLVIVTADHAHASQIVA
PDTKAPGLTQALNTKDGAVM
VMSYGNSEEDSQEHTGSQLR
IAAYGPHAANVVGLTDQTDL
FYTMKAALGLK
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 799 |
15N chemical shifts | 599 |
1H chemical shifts | 1328 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity_1, 1 | 1 |
2 | entity_2 | 2 |
3 | entity_1, 2 | 1 |
Entities:
Entity 1, entity_1, 1 280 residues - 31023.424 Da.
1 | MET | ALA | ALA | LYS | LYS | ASP | TYR | TYR | ALA | ILE | |
2 | LEU | GLY | VAL | PRO | ARG | ASN | ALA | THR | GLN | GLU | |
3 | GLU | ILE | LYS | ARG | ALA | TYR | LYS | ARG | LEU | ALA | |
4 | ARG | GLN | TYR | HIS | PRO | ASP | VAL | ASN | LYS | SER | |
5 | PRO | GLU | ALA | GLU | GLU | LYS | PHE | LYS | GLU | ILE | |
6 | ASN | GLU | ALA | TYR | ALA | VAL | LEU | SER | ASP | PRO | |
7 | GLU | LYS | ARG | ARG | ILE | TYR | ASP | THR | TYR | GLY | |
8 | THR | THR | GLU | ALA | PRO | PRO | PRO | PRO | PRO | PRO | |
9 | GLY | GLY | TYR | ASP | PHE | SER | GLY | PHE | ASP | VAL | |
10 | GLU | ASP | PHE | SER | GLU | PHE | PHE | GLN | GLU | LEU | |
11 | PHE | GLY | PRO | GLY | LEU | PHE | GLY | GLY | PHE | GLY | |
12 | ARG | ARG | SER | ARG | LYS | GLY | ARG | ASP | LEU | ARG | |
13 | ALA | GLU | LEU | PRO | LEU | THR | LEU | GLU | GLU | ALA | |
14 | PHE | HIS | GLY | GLY | GLU | ARG | VAL | VAL | GLU | VAL | |
15 | ALA | GLY | ARG | ARG | VAL | SER | VAL | ARG | ILE | PRO | |
16 | PRO | GLY | VAL | ARG | GLU | GLY | SER | VAL | ILE | ARG | |
17 | VAL | PRO | GLY | MET | GLY | GLY | GLN | GLY | ASN | PRO | |
18 | PRO | GLY | ASP | LEU | LEU | LEU | VAL | VAL | ARG | LEU | |
19 | LEU | PRO | HIS | PRO | VAL | PHE | ARG | LEU | GLU | GLY | |
20 | GLN | ASP | LEU | TYR | ALA | THR | LEU | ASP | VAL | PRO | |
21 | ALA | PRO | ILE | ALA | VAL | VAL | GLY | GLY | LYS | VAL | |
22 | ARG | ALA | MET | THR | LEU | GLU | GLY | PRO | VAL | GLU | |
23 | VAL | ALA | VAL | PRO | PRO | ARG | THR | GLN | ALA | GLY | |
24 | ARG | LYS | LEU | ARG | LEU | LYS | GLY | LYS | GLY | PHE | |
25 | PRO | GLY | PRO | ALA | GLY | ARG | GLY | ASP | LEU | TYR | |
26 | LEU | GLU | VAL | ARG | ILE | THR | ILE | PRO | GLU | ARG | |
27 | LEU | THR | PRO | GLU | GLU | GLU | ALA | LEU | TRP | LYS | |
28 | LYS | LEU | ALA | GLU | ALA | TYR | TYR | ALA | ARG | ALA |
Entity 2, entity_2 471 residues - 49492.367 Da.
1 | MET | LYS | GLN | SER | THR | ILE | ALA | LEU | ALA | LEU | ||||
2 | LEU | PRO | LEU | LEU | PHE | THR | PRO | VAL | THR | LYS | ||||
3 | ALA | ARG | THR | PRO | GLU | MET | PRO | VAL | LEU | GLU | ||||
4 | ASN | ARG | ALA | ALA | GLN | GLY | ASP | ILE | THR | ALA | ||||
5 | PRO | GLY | GLY | ALA | ARG | ARG | LEU | THR | GLY | ASP | ||||
6 | GLN | THR | ALA | ALA | LEU | ARG | ASP | SER | LEU | SER | ||||
7 | ASP | LYS | PRO | ALA | LYS | ASN | ILE | ILE | LEU | LEU | ||||
8 | ILE | GLY | ASP | GLY | MET | GLY | ASP | SER | GLU | ILE | ||||
9 | THR | ALA | ALA | ARG | ASN | TYR | ALA | GLU | GLY | ALA | ||||
10 | GLY | GLY | PHE | PHE | LYS | GLY | ILE | ASP | ALA | LEU | ||||
11 | PRO | LEU | THR | GLY | GLN | TYR | THR | HIS | TYR | ALA | ||||
12 | LEU | ASN | LYS | LYS | THR | GLY | LYS | PRO | ASP | TYR | ||||
13 | VAL | THR | ASP | SER | ALA | ALA | SER | ALA | THR | ALA | ||||
14 | TRP | SER | THR | GLY | VAL | LYS | THR | TYR | ASN | GLY | ||||
15 | ALA | LEU | GLY | VAL | ASP | ILE | HIS | GLU | LYS | ASP | ||||
16 | HIS | PRO | THR | ILE | LEU | GLU | MET | ALA | LYS | ALA | ||||
17 | ALA | GLY | LEU | ALA | THR | GLY | ASN | VAL | SER | THR | ||||
18 | ALA | GLU | LEU | GLN | ASP | ALA | THR | PRO | ALA | ALA | ||||
19 | LEU | VAL | ALA | HIS | VAL | THR | SER | ARG | LYS | CYS | ||||
20 | TYR | GLY | PRO | SER | ALA | THR | SER | GLU | LYS | CYS | ||||
21 | PRO | GLY | ASN | ALA | LEU | GLU | LYS | GLY | GLY | LYS | ||||
22 | GLY | SER | ILE | THR | GLU | GLN | LEU | LEU | ASN | ALA | ||||
23 | ARG | ALA | ASP | VAL | THR | LEU | GLY | GLY | GLY | ALA | ||||
24 | LYS | THR | PHE | ALA | GLU | THR | ALA | THR | ALA | GLY | ||||
25 | GLU | TRP | GLN | GLY | LYS | THR | LEU | ARG | GLU | GLN | ||||
26 | ALA | GLN | ALA | ARG | GLY | TYR | GLN | LEU | VAL | SER | ||||
27 | ASP | ALA | ALA | SER | LEU | ASN | SER | VAL | THR | GLU | ||||
28 | ALA | ASN | GLN | GLN | LYS | PRO | LEU | LEU | GLY | LEU | ||||
29 | PHE | ALA | ASP | GLY | ASN | MET | PRO | VAL | ARG | TRP | ||||
30 | LEU | GLY | PRO | LYS | ALA | THR | TYR | HIS | GLY | ASN | ||||
31 | ILE | ASP | LYS | PRO | ALA | VAL | THR | CYS | THR | PRO | ||||
32 | ASN | PRO | GLN | ARG | ASN | ASP | SER | VAL | PRO | THR | ||||
33 | LEU | ALA | GLN | MET | THR | ASP | LYS | ALA | ILE | GLU | ||||
34 | LEU | LEU | SER | LYS | ASN | GLU | LYS | GLY | PHE | PHE | ||||
35 | LEU | GLN | VAL | GLU | GLY | ALA | SER | ILE | ASP | LYS | ||||
36 | GLN | ASP | HIS | ALA | ALA | ASN | PRO | CYS | GLY | GLN | ||||
37 | ILE | GLY | GLU | THR | VAL | ASP | LEU | ASP | GLU | ALA | ||||
38 | VAL | GLN | ARG | ALA | LEU | GLU | PHE | ALA | LYS | LYS | ||||
39 | GLU | GLY | ASN | THR | LEU | VAL | ILE | VAL | THR | ALA | ||||
40 | ASP | HIS | ALA | HIS | ALA | SER | GLN | ILE | VAL | ALA | ||||
41 | PRO | ASP | THR | LYS | ALA | PRO | GLY | LEU | THR | GLN | ||||
42 | ALA | LEU | ASN | THR | LYS | ASP | GLY | ALA | VAL | MET | ||||
43 | VAL | MET | SER | TYR | GLY | ASN | SER | GLU | GLU | ASP | ||||
44 | SER | GLN | GLU | HIS | THR | GLY | SER | GLN | LEU | ARG | ||||
45 | ILE | ALA | ALA | TYR | GLY | PRO | HIS | ALA | ALA | ASN | ||||
46 | VAL | VAL | GLY | LEU | THR | ASP | GLN | THR | ASP | LEU | ||||
47 | PHE | TYR | THR | MET | LYS | ALA | ALA | LEU | GLY | LEU | ||||
48 | LYS |
Samples:
sample_1: PhoA_DnaJ, [U-100% 13C; U-100% 15N; U-80% 2H], 1 mM; potassium chloride 75 mM; potassium phosphate 20 mM; sodium azide 0.04%
sample_conditions_1: ionic strength: 100 mM; pH: 7; pressure: 1 atm; temperature: 25 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HMQC | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D CNH-sofast hmqc-NOESY-hmqc | sample_1 | isotropic | sample_conditions_1 |
3D HNH-sofastNOESY-hmqc | sample_1 | isotropic | sample_conditions_1 |
3D HCH-sofastNOESY-hmqc | sample_1 | isotropic | sample_conditions_1 |
3D NCH-sofast hmqc-NOESY-hmqc | sample_1 | isotropic | sample_conditions_1 |
3D CCH-sofast hmqc-NOESY-hmqc | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
Software:
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
CYANA, Guntert, Mumenthaler and Wuthrich - structure calculation
PINE, Bahrami, Markley, Assadi, and Eghbalnia - chemical shift assignment
Sparky, Goddard - peak picking
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
TALOS, Cornilescu, Delaglio and Bax - geometry optimization
TopSpin, Bruker Biospin - collection
PSVS, Bhattacharya and Montelione - processing
NMR spectrometers:
- Bruker AVANCE NEO 700 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts