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9EN6

Crystal structure of RNA G2C4 repeats - native model pH 6.5

This is a non-PDB format compatible entry.
Summary for 9EN6
Entry DOI10.2210/pdb9en6/pdb
Related8QMH 8QMI
DescriptorRNA (5'-R(*GP*GP*CP*CP*CP*C)-3'), MAGNESIUM ION (3 entities in total)
Functional Keywordsrna, g2c4 repeats, als, ftd, hexanucleotide repeats
Biological sourceHomo sapiens
Total number of polymer chains4
Total formula weight7537.64
Authors
Mateja-Pluta, M.,Kiliszek, A. (deposition date: 2024-03-12, release date: 2024-05-01, Last modification date: 2024-07-03)
Primary citationBlaszczyk, L.,Ryczek, M.,Das, B.,Mateja-Pluta, M.,Bejger, M.,Sliwiak, J.,Nakatani, K.,Kiliszek, A.
Antisense RNA C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms a triplex-like structure and binds small synthetic ligand.
Nucleic Acids Res., 52:6707-6717, 2024
Cited by
PubMed Abstract: The abnormal expansion of GGGGCC/GGCCCC hexanucleotide repeats (HR) in C9orf72 is associated with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Structural polymorphisms of HR result in the multifactorial pathomechanism of ALS/FTD. Consequently, many ongoing studies are focused at developing therapies targeting pathogenic HR RNA. One of them involves small molecules blocking sequestration of important proteins, preventing formation of toxic nuclear foci. However, rational design of potential therapeutics is hindered by limited number of structural studies of RNA-ligand complexes. We determined the crystal structure of antisense HR RNA in complex with ANP77 ligand (1.1 Å resolution) and in the free form (0.92 and 1.5 Å resolution). HR RNA folds into a triplex structure composed of four RNA chains. ANP77 interacted with two neighboring single-stranded cytosines to form pseudo-canonical base pairs by adopting sandwich-like conformation and adjusting the position of its naphthyridine units to the helical twist of the RNA. In the unliganded structure, the cytosines formed a peculiar triplex i-motif, assembled by trans C•C+ pair and a third cytosine located at the Hoogsteen edge of the C•C+ pair. These results extend our knowledge of the structural polymorphisms of HR and can be used for rational design of small molecules targeting disease-related RNAs.
PubMed: 38738637
DOI: 10.1093/nar/gkae376
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (0.918 Å)
Structure validation

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PDB entries from 2024-11-06

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