36OU image
Deposition Date 2026-06-24
Release Date 2026-11-04
Last Version Date 2026-11-04
Entry Detail
PDB ID:
36OU
Title:
Room-temperature multiconformer model of PSD-95 PDZ3-CRIPT
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.35 Å
R-Value Free:
0.14
R-Value Work:
0.12
R-Value Observed:
0.12
Space Group:
P 41 3 2
Macromolecular Entities
Polymer Type:polypeptide(L)
Molecule:Disks large homolog 4
Gene (Uniprot):Dlg4
Chain IDs:A
Chain Length:119
Number of Molecules:1
Biological Source:Rattus norvegicus
Polymer Type:polypeptide(L)
Molecule:Cysteine-rich PDZ-binding pro
Gene (Uniprot):Cript
Chain IDs:B
Chain Length:9
Number of Molecules:1
Biological Source:Rattus norvegicus
Primary Citation
Symmetry Breaking under Vectorial Perturbations in Macromolecular X-ray Crystallography.
Biorxiv ? ? ? (2026)
PMID: 42856210 DOI: 10.64898/2026.09.28.753211

Abstact

Proteins are molecular machines whose dynamics govern their function. Using time-resolved crystallography, the basis of protein mechanics can be uncovered by physical perturbation on protein crystals. Perturbations are often vector fields that, in crystals, break symmetry. Lacking existing tools for analyzing symmetry breaking, we built open-source software to do so. We applied this method to three time-resolved crystallography experiments and analyzed the effect of vectorial perturbations on macromolecular crystal structure. We demonstrate that our method can handle symmetry reduction in all 65 Sohncke space groups.

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Primary Citation of related structures
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