Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6OWZ

Spy H96L:Im7 L19pI-Phe complex; multiple anomalous datasets contained herein for element identification

Summary for 6OWZ
Entry DOI10.2210/pdb6owz/pdb
DescriptorPeriplasmic chaperone Spy, ZINC ION, CHLORIDE ION, ... (6 entities in total)
Functional Keywordsperiplasmic, chaperone
Biological sourceEscherichia coli
Total number of polymer chains2
Total formula weight24535.85
Authors
Rocchio, S.,Duman, R.,El Omari, K.,Mykhaylyk, V.,Yan, Z.,Wagner, A.,Bardwell, J.C.A.,Horowitz, S. (deposition date: 2019-05-12, release date: 2019-05-29, Last modification date: 2023-10-11)
Primary citationRocchio, S.,Duman, R.,El Omari, K.,Mykhaylyk, V.,Orr, C.,Yan, Z.,Salmon, L.,Wagner, A.,Bardwell, J.C.A.,Horowitz, S.
Identifying dynamic, partially occupied residues using anomalous scattering.
Acta Crystallogr D Struct Biol, 75:1084-1095, 2019
Cited by
PubMed Abstract: Although often presented as taking single `snapshots' of the conformation of a protein, X-ray crystallography provides an averaged structure over time and space within the crystal. The important but difficult task of characterizing structural ensembles in crystals is typically limited to small conformational changes, such as multiple side-chain conformations. A crystallographic method was recently introduced that utilizes residual electron and anomalous density (READ) to characterize structural ensembles encompassing large-scale structural changes. Key to this method is an ability to accurately measure anomalous signals and distinguish them from noise or other anomalous scatterers. This report presents an optimized data-collection and analysis strategy for partially occupied iodine anomalous signals. Using the long-wavelength-optimized beamline I23 at Diamond Light Source, the ability to accurately distinguish the positions of anomalous scatterers with occupancies as low as ∼12% is demonstrated. The number and positions of these anomalous scatterers are consistent with previous biophysical, kinetic and structural data that suggest that the protein Im7 binds to the chaperone Spy in multiple partially occupied conformations. Finally, READ selections demonstrate that re-measured data using the new protocols are consistent with the previously characterized structural ensemble of the chaperone Spy with its client Im7. This study shows that a long-wavelength beamline results in easily validated anomalous signals that are strong enough to be used to detect and characterize highly disordered sections of crystal structures.
PubMed: 31793902
DOI: 10.1107/S2059798319014475
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

227111

数据于2024-11-06公开中

PDB statisticsPDBj update infoContact PDBjnumon