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4Z7L

Crystal structure of Cas6b

Summary for 4Z7L
Entry DOI10.2210/pdb4z7l/pdb
Related4Z7K
DescriptorCas6b, RNA (5'-R(*GP*CP*AP*AP*AP*AP*UP*AP*AP*CP*AP*AP*GP*C)-3'), SULFATE ION (3 entities in total)
Functional Keywordscrispr rna, endoribonucleases, hydrolase-rna complex, hydrolase/rna
Biological sourceMethanococcus maripaludis (strain C5 / ATCC BAA-1333)
More
Total number of polymer chains9
Total formula weight167123.91
Authors
Li, H. (deposition date: 2015-04-07, release date: 2016-04-13, Last modification date: 2024-03-06)
Primary citationShao, Y.,Richter, H.,Sun, S.,Sharma, K.,Urlaub, H.,Randau, L.,Li, H.
A Non-Stem-Loop CRISPR RNA Is Processed by Dual Binding Cas6.
Structure, 24:547-554, 2016
Cited by
PubMed Abstract: A subclass of recently discovered CRISPR repeat RNA in bacteria contains minimally recognizable structural features that facilitate an unknown mechanism of recognition and processing by the Cas6 family of endoribonucleases. Cocrystal structures of Cas6 from Methanococcus maripaludis (MmCas6b) bound with its repeat RNA revealed a dual site binding structure and a cleavage site conformation poised for phosphodiester bond breakage. Two non-interacting MmCas6b bind to two separate AAYAA motifs within the same repeat, one distal and one adjacent to the cleavage site. This bound structure potentially competes with a stable but non-productive RNA structure. At the cleavage site, MmCas6b supplies a base pair mimic to stabilize a short 2 base pair stem immediately upstream of the scissile phosphate. Complementary biochemical analyses support the dual-AAYAA binding model and a critical role of the protein-RNA base pair mimic. Our results reveal a previously unknown method of processing non-stem-loop CRISPR RNA by Cas6.
PubMed: 26996962
DOI: 10.1016/j.str.2016.02.009
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.503 Å)
Structure validation

237735

數據於2025-06-18公開中

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