wwPDB validation report of PDB entry 2AQ2

the G17E/S54N/L81S variant of the murine T cell receptor V beta 8.2 domain

the G17E/A52V/S54N/K66E/L81S variant of the murine T cell receptor V beta 8.2 domain

the G17E/S54N/K66E/Q72H/E80V/L81S/T87S/G96V variant of the murine T cell receptor V beta 8.2 domain

the G17E/A52V/S54N/Q72H/E80V/L81S/T87S/G96V variant of the murine T cell receptor V beta 8.2 domain

the G17E/A52V/S54N/K66E/E80V/L81S/T87S/G96V variant of the murine T cell receptor V beta 8.2 domain

the G17E/A52V/S54N/K66E/Q72H/E80V/L81S/T87S/G96V variant of the murine T cell receptor V beta 8.2 domain

T-Cell receptor V beta domain variant (G17E/A52V/S54N/K66E/E80V/L81S/T87S/G96V) complexed with superantigen SEC3 mutant

T-Cell receptor V beta domain variant (G17E/L81S) complexed with superantigen SEC3 mutant

HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS

T-CELL RECEPTOR BETA CHAIN V, Enterotoxin type C-3
Crystal structure of T-cell receptor V beta domain variant complexed with superantigen SEC3 mutant

The largest off-origin peak in the Patterson function is 4.10% of the height of the origin peak. No significant pseudotranslation is detected.

20191225.v01 (using entries in the PDB archive December 25th 2019)

structure factor analysis and validation

geometric validation package for ligand chemistry in protein x-ray structures