9L12
Crystal structure of Cas12h ternary complex
Summary for 9L12
| Entry DOI | 10.2210/pdb9l12/pdb |
| Descriptor | Cas12h, DNA (28-MER), DNA (5'-D(P*AP*GP*TP*CP*GP*AP*TP*GP*TP*TP*CP*T)-3'), ... (5 entities in total) |
| Functional Keywords | rna, dna, complex, dna binding protein |
| Biological source | unidentified More |
| Total number of polymer chains | 12 |
| Total formula weight | 394033.29 |
| Authors | |
| Primary citation | Xiang, W.,Lin, X.,Yang, Y.,Huang, L.,Chen, Y.,Chen, J.,Liu, L. Cas12h is a crRNA-guided DNA nickase that can be utilized for precise gene editing. Cell Rep, 44:115718-115718, 2025 Cited by PubMed Abstract: Type V-H CRISPR-Cas system, an important subtype of type V CRISPR-Cas systems, has remained enigmatic in terms of its structure and function despite being discovered several years ago. Here, we comprehensively characterize the type V-H CRISPR-Cas system and elucidate its role as a DNA nicking system. The unique CRISPR RNA (crRNA) employed by Cas12h effector protein enables specific targeting of double-stranded DNA (dsDNA), while its RuvC domain is responsible for cleaving the non-target strand (NTS) of dsDNA. We present the structure of Cas12h bound to crRNA and target DNA. Our structural analysis reveals that the RuvC domain possesses a narrow active pocket that facilitates recognition of NTS but potentially hinders access to the target strand. Furthermore, we demonstrate that Cas12h confers adaptive immunity against invading mobile genetic elements through transcriptional gene inhibition. We have engineered an adenine base editor by fusing Cas12h with an adenine deaminase, achieving effective A-to-G substitution. PubMed: 40372912DOI: 10.1016/j.celrep.2025.115718 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.81 Å) |
Structure validation
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