#IFEStandardized nameMoleculeOrganismSourceRfamTitleMethodRes. ÅDate
17DCO|1|B (rep)U5 spliceosomal RNApre-mRNA, U5 snRNASaccharomyces cerevisiaeEukaryaRF00020Cryo-EM structure of the activated spliceosome (Bact complex) at an atomic resolution of 2.5 angstromElectron microscopy2.52021-03-17
27B9V|1|5U5 spliceosomal RNA5' exon of UBC4 mRNA, U5 snRNASaccharomyces cerevisiaeEukaryaRF00020Yeast C complex spliceosome at 2.8 Angstrom resolution with Prp18/Slu7 boundElectron microscopy2.82021-03-10
36J6G|1|DU5 spliceosomal RNAACT1 pre-mRNA, U5 snRNASaccharomyces cerevisiaeEukaryaRF00020Cryo-EM structure of the yeast B*-a2 complex at an average resolution of 3.2 angstromElectron microscopy3.22019-04-24
46BK8|1|5U5 spliceosomal RNARNA (34-MER), U5 snRNASaccharomyces cerevisiaeEukaryaRF00020S. cerevisiae spliceosomal post-catalytic P complexElectron microscopy3.32018-02-21
55GMK|1|DU5 spliceosomal RNA5'-Exon, U5 snRNASaccharomyces cerevisiaeEukaryaRF00020Cryo-EM structure of the Catalytic Step I spliceosome (C complex) at 3.4 angstrom resolutionElectron microscopy3.42016-08-17
65GM6|1|DU5 spliceosomal RNASaccharomyces cerevisiae strain CDRDR_sf_H chromosome VII sequenceSaccharomyces cerevisiaeEukaryaRF00020Cryo-EM structure of the activated spliceosome (Bact complex) at 3.5 angstrom resolutionElectron microscopy3.52016-09-21
75Y88|1|BU5 spliceosomal RNAU5 snRNASaccharomyces cerevisiaeEukaryaRF00020Cryo-EM structure of the intron-lariat spliceosome ready for disassembly from S.cerevisiae at 3.5 angstromElectron microscopy3.462018-08-01

Release history

Release3.3443.3453.3463.3473.3483.3493.3503.3513.3523.3533.3543.3553.3563.3573.3583.3593.3603.3613.362
Date2024-07-172024-07-252024-07-312024-08-072024-08-142024-08-212024-08-282024-09-042024-09-112024-09-182024-09-252024-10-022024-10-092024-10-162024-10-232024-10-302024-11-062024-11-132024-11-20

Parents

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Children

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Instances are ordered to put similar structures near each other. Select one instance to see its 3D structure. Selecting two or more instances will show their superposition, but only chains with identical numbers of observed nucleotides will superpose well. Large structures are slow to display; this tool is not designed for that.

#SViewPDBTitleMethodResolutionLength
17DCO|1|BCryo-EM structure of the activated spliceosome (Bact complex) at an atomic resolution of 2.5 angstromELECTRON MICROSCOPY2.5179
26BK8|1|5S. cerevisiae spliceosomal post-catalytic P complexELECTRON MICROSCOPY3.3103
35GMK|1|DCryo-EM structure of the Catalytic Step I spliceosome (C complex) at 3.4 angstrom resolutionELECTRON MICROSCOPY3.4117
45Y88|1|BCryo-EM structure of the intron-lariat spliceosome ready for disassembly from S.cerevisiae at 3.5 angstromELECTRON MICROSCOPY3.46117
55GM6|1|DCryo-EM structure of the activated spliceosome (Bact complex) at 3.5 angstrom resolutionELECTRON MICROSCOPY3.5117
66J6G|1|DCryo-EM structure of the yeast B*-a2 complex at an average resolution of 3.2 angstromELECTRON MICROSCOPY3.2179
77B9V|1|5Yeast C complex spliceosome at 2.8 Angstrom resolution with Prp18/Slu7 boundELECTRON MICROSCOPY2.8178

Heat map of mutual geometric discrepancy, in Angstroms per nucleotide. The ordering in the heat map is the same as in the table. The colorbar ranges from 0 to the maximum observed discrepancy. Click above the diagonal to select a range of structures, below the diagonal to select two structures.


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