BMRB Entry 18201
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                Entry in NMR Restraints Grid
                Validation report in NRG-CING
            Chem Shift validation:  AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR18201
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Title: 1H, 13C and 15N resonance assignments of the periplasmic signaling domain of HasR, a TonB-dependent outer membrane heme transporter PubMed: 22415545
Deposition date: 2012-01-18 Original release date: 2012-03-23
Authors: Malki, Idir; Cardoso de Amorim, Gisele; Simenel, Catherine; Prochnicka-Chalufour, Ada; Delepierre, Muriel; Izadi-Pruneyre, Nadia
Citation: Malki, Idir; Cardoso de Amorim, Gisele; Simenel, Catherine; Prochnicka-Chalufour, Ada; Delepierre, Muriel; Izadi-Pruneyre, Nadia. "(1)H, (13)C and (15)N resonance assignments of the periplasmic signalling domain of HasR, a TonB-dependent outer membrane heme transporter." Biomol. NMR Assignments 7, 43-46 (2013).
Assembly members:
HasR_N-terminal_periplasmic_signaling_domain, polymer, 107 residues,  Formula weight is not available
Natural source: Common Name: Serratia marcescens Taxonomy ID: 615 Superkingdom: Bacteria Kingdom: not available Genus/species: Serratia marcescens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
HasR_N-terminal_periplasmic_signaling_domain: SMAQAAQQKNFNIAAQPLQS
AMLRFAEQAGMQVFFDEVKL
DGMQAAALNGSMSVEQGLRR
LIGGNPVAFRLQPQGQIVLS
RLPTANGDGGALALDSLTVL
GAGGNNA
- assigned_chemical_shifts
 
| Data type | Count | 
| 13C chemical shifts | 403 | 
| 15N chemical shifts | 107 | 
| 1H chemical shifts | 657 | 
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID | 
|---|---|---|
| 1 | HasR N-terminal periplasmic signaling domain | 1 | 
Entities:
Entity 1, HasR N-terminal periplasmic signaling domain 107 residues - Formula weight is not available
| 1 | SER | MET | ALA | GLN | ALA | ALA | GLN | GLN | LYS | ASN | ||||
| 2 | PHE | ASN | ILE | ALA | ALA | GLN | PRO | LEU | GLN | SER | ||||
| 3 | ALA | MET | LEU | ARG | PHE | ALA | GLU | GLN | ALA | GLY | ||||
| 4 | MET | GLN | VAL | PHE | PHE | ASP | GLU | VAL | LYS | LEU | ||||
| 5 | ASP | GLY | MET | GLN | ALA | ALA | ALA | LEU | ASN | GLY | ||||
| 6 | SER | MET | SER | VAL | GLU | GLN | GLY | LEU | ARG | ARG | ||||
| 7 | LEU | ILE | GLY | GLY | ASN | PRO | VAL | ALA | PHE | ARG | ||||
| 8 | LEU | GLN | PRO | GLN | GLY | GLN | ILE | VAL | LEU | SER | ||||
| 9 | ARG | LEU | PRO | THR | ALA | ASN | GLY | ASP | GLY | GLY | ||||
| 10 | ALA | LEU | ALA | LEU | ASP | SER | LEU | THR | VAL | LEU | ||||
| 11 | GLY | ALA | GLY | GLY | ASN | ASN | ALA | 
Samples:
sample_1: HasR_N-terminal_periplasmic_signaling_domain, [U-99% 13C; U-99% 15N], 0.5 mM; Sodium phosphate 50 mM; NaCl 50 mM
sample_conditions_1: ionic strength: 0.1 M; pH: 7.0; pressure: 1 atm; temperature: 293 K
Experiments:
| Name | Sample | Sample state | Sample conditions | 
|---|---|---|---|
| 2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 | 
| 2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 | 
| 3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D HNCACB | sample_1 | isotropic | sample_conditions_1 | 
| 3D HNCO | sample_1 | isotropic | sample_conditions_1 | 
| 3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 | 
| 2D HbCbCgCdHd | sample_1 | isotropic | sample_conditions_1 | 
| 2D HbCbCgCdCeHe | sample_1 | isotropic | sample_conditions_1 | 
Software:
ANALYSIS v2.15, CCPN - chemical shift assignment
NMR spectrometers:
- Varian NMR System 600 MHz
 
Related Database Links:
| PDB | |
| DBJ | BAO32406 | 
| EMBL | CAE46936 CDG10875 | 
| GB | ALL36750 EMF03485 ERH72206 ETX40680 KFD10590 | 
| REF | WP_004940484 WP_016928899 WP_019454232 WP_021504699 WP_025301725 | 
Download simulated HSQC data in one of the following formats:
            
CSV: Backbone
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SPARKY: Backbone
            or all simulated shifts