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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | NER dual incision complex - NoG consensus map | |||||||||
Map data | NER dual incision complex - NoG consensus map | |||||||||
Sample |
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Keywords | NER / XPA / XPG / XPF / DNA binding protein | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.24 Å | |||||||||
Authors | Kim J / Li CL / Yang W | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nature / Year: 2026Title: Pre-incision structures reveal principles of DNA nucleotide excision repair. Authors: Eric C L Li / Jinseok Kim / Sem J Brussee / Kaoru Sugasawa / Martijn S Luijsterburg / Wei Yang / ![]() Abstract: Nucleotide excision repair (NER) removes bulky adducts from genomic DNA and prevents the ultraviolet light-sensitivity disease xeroderma pigmentosum, cancer and premature ageing. After initial lesion ...Nucleotide excision repair (NER) removes bulky adducts from genomic DNA and prevents the ultraviolet light-sensitivity disease xeroderma pigmentosum, cancer and premature ageing. After initial lesion recognition by XPC in global genome repair or by stalled RNA polymerases in transcription-coupled repair, a lesion and surrounding DNA duplex are unwound by TFIIH, which includes the ATPases XPB and XPD, and additional NER factors XPA, XPF, XPG and RPA, to form a DNA bubble comprising around 27 nucleotides. The double strand-single strand (ds-ss) junction-specific endonucleases XPF and XPG cleave DNA on the 5' and 3' sides of the lesion, respectively. Here we report the functional steps and atomic structures of the ATPase-driven and lesion-dependent DNA bubble formation and arrangement of the complete NER factors for dual incision. The unwinding of nearly 30 base pairs of DNA depends mainly on the double strand DNA translocase XPB and the duplex dividers XPA and XPF. XPD binds the lesion strand with XPF at the 5' ds-ss junction. XPF cuts the lesion strand only after XPG binds the 3' ds-ss junction. The ERCC1 subunit of XPF facilitates DNA strand separation and recruitment of RPA to the non-lesion strand. These findings provide insights on the causes of human diseases and potential targets for enhancing chemotherapeutic efficacy. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_75693.map.gz | 4 MB | EMDB map data format | |
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| Header (meta data) | emd-75693-v30.xml emd-75693.xml | 21.7 KB 21.7 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_75693_fsc.xml | 7.8 KB | Display | FSC data file |
| Images | emd_75693.png | 112.4 KB | ||
| Masks | emd_75693_msk_1.map | 40.6 MB | Mask map | |
| Filedesc metadata | emd-75693.cif.gz | 4.8 KB | ||
| Others | emd_75693_additional_1.map.gz emd_75693_half_map_1.map.gz emd_75693_half_map_2.map.gz | 31.2 MB 31.3 MB 31.3 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-75693 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-75693 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_75693.map.gz / Format: CCP4 / Size: 40.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | NER dual incision complex - NoG consensus map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.66 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_75693_msk_1.map | ||||||||||||
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-Additional map: Additional Map
| File | emd_75693_additional_1.map | ||||||||||||
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| Annotation | Additional Map | ||||||||||||
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| Density Histograms |
-Half map: Half Map A
| File | emd_75693_half_map_1.map | ||||||||||||
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| Annotation | Half Map A | ||||||||||||
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| Density Histograms |
-Half map: Half Map B
| File | emd_75693_half_map_2.map | ||||||||||||
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| Annotation | Half Map B | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : NER dual incision complex without XPG
| Entire | Name: NER dual incision complex without XPG |
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| Components |
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-Supramolecule #1: NER dual incision complex without XPG
| Supramolecule | Name: NER dual incision complex without XPG / type: complex / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 880 KDa |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 0.6 mg/mL | |||||||||||||||||||||
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| Buffer | pH: 7.9 Component:
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| Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 300 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. | |||||||||||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 55.8 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.4 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 105000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi




Keywords
Homo sapiens (human)
Authors
United States, 1 items
Citation













Z (Sec.)
Y (Row.)
X (Col.)




















































Processing
FIELD EMISSION GUN

