BMRB Entry 34091
Click here to enlarge.
            
                PDB ID: 
                
                
                Entry in NMR Restraints Grid
                Validation report in NRG-CING
            Chem Shift validation:  AVS_full
BMRB Entry DOI: doi:10.13018/BMR34091
MolProbity Validation Chart            
                    NMR-STAR file interactive viewer.
                    NMR-STAR v3 text file.
                    NMR-STAR v2.1 text file (deprecated)
                    XML gzip file.
                    RDF gzip file.
                    All files associated with the entry
                
Title: Peptide-membrane interaction between targeting and lysis PubMed: 28763193
Deposition date: 2017-01-24 Original release date: 2017-02-16
Authors: Schneider, G.; Blatter, M.
Citation: Stutz, Katharina; Muller, Alex; Hiss, Jan; Schneider, Petra; Blatter, Markus; Pfeiffer, Bernhard; Posselt, Gernot; Kanfer, Gil; Kornmann, Benoit; Wrede, Paul; Altmann, Karl-Heinz; Wessler, Silja; Schneider, Gisbert. "Peptide-Membrane Interaction between Targeting and Lysis." ACS Chem. Biol. 12, 2254-2259 (2017).
Assembly members:
entity_1, polymer, 15 residues,   1851.080 Da.
Natural source: Common Name: not available Taxonomy ID: 32630 Superkingdom: not available Kingdom: not available Genus/species: not available not available
Experimental source: Production method: recombinant technology Host organism: synthetic construct
Entity Sequences (FASTA):
entity_1: WYHRLSHLHSRLQDX
- assigned_chemical_shifts
 
| Data type | Count | 
| 13C chemical shifts | 55 | 
| 1H chemical shifts | 103 | 
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID | 
|---|---|---|
| 1 | entity_1 | 1 | 
Entities:
Entity 1, entity_1 15 residues - 1851.080 Da.
| 1 | TRP | TYR | HIS | ARG | LEU | SER | HIS | LEU | HIS | SER | ||||
| 2 | ARG | LEU | GLN | ASP | NH2 | 
Samples:
sample_1: peptide 100%
sample_conditions_1: ionic strength: 100 mM; pH: 7.0; pressure: 1 atm; temperature: 293 K
Experiments:
| Name | Sample | Sample state | Sample conditions | 
|---|---|---|---|
| NOESY STRUCTURE a DETERMINATION. | sample_1 | anisotropic | sample_conditions_1 | 
Software:
AMBER v3.97, Case, Darden, Cheatham III, Simmerling, Wang, Duke, Luo, ... and Kollman - refinement
CYANA v3.97, Guntert, Mumenthaler and Wuthrich - structure calculation
NMR spectrometers:
- Bruker AvanceIII 500 MHz