wwPDB validation report of PDB entry 2VOO

HUMAN LA PROTEIN, SJOEGREN SYNDROME TYPE B ANTIGEN, SS-B, LA RIBONUCLEOPROTEIN, LA AUTOANTIGEN

NMR STRUCTURE OF THE LA MOTIF OF HUMAN LA PROTEIN

STRUCTURAL BASIS FOR RECOGNITION OF UUUOH 3 '-TERMINII OFNASCENT RNA POL III TRANSCRIPTS BY LA AUTOANTIGEN

SOLUTION STRUCTURE OF THE CENTRAL RRM OF HUMAN LA PROTEIN

CRYSTAL STRUCTURE OF N-TERMINAL DOMAINS OF HUMAN LA PROTEIN COMPLEXED WITH RNA OLIGOMER AUAUUUU

CRYSTAL STRUCTURE OF N-TERMINAL DOMAINS OF HUMAN LA PROTEIN COMPLEXED WITH RNA OLIGOMER AUUUU

SOLUTION STRUCTURE OF THE C-TERMINAL RRM OF HUMAN LA (LA225-334)

FIRST TWO RESIDUES ARE FROM VECTOR (GS) REMAINS, SEQUENCE CORRESPONDS RESIDUES 4-194

Crystal structure of N-terminal domains of Human La protein complexed with RNA oligomer UUUUUUUU

The analyses of the Patterson function reveals a significant off-origin peak that is 59.10 % of the origin peak, indicating pseudo-translational symmetry. The chance of finding a peak of this or larger height by random in a structure without pseudo-translational symmetry is equal to 1.8544e-05. The detected translational NCS is most likely also responsible for the elevated intensity ratio. See the relevant section of the logfile for more details.

structure factor analysis and validation

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

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