+
Open data
-
Basic information
| Entry | Database: PDB / ID: 9hql | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Title | UP1 in complex with Z1152242726 | |||||||||
Components | Heterogeneous nuclear ribonucleoprotein A1, N-terminally processed | |||||||||
Keywords | RNA BINDING PROTEIN / fragment screening / hnRNP A1 / UP1 / RNA/DNA BINDING PROTEIN / UP1-fragment complex | |||||||||
| Function / homology | Function and homology informationcellular response to sodium arsenite / SARS-CoV-1-host interactions / import into nucleus / telomeric repeat-containing RNA binding / alternative mRNA splicing, via spliceosome / G-rich strand telomeric DNA binding / pre-mRNA binding / nuclear export / RNA export from nucleus / miRNA binding ...cellular response to sodium arsenite / SARS-CoV-1-host interactions / import into nucleus / telomeric repeat-containing RNA binding / alternative mRNA splicing, via spliceosome / G-rich strand telomeric DNA binding / pre-mRNA binding / nuclear export / RNA export from nucleus / miRNA binding / FGFR2 alternative splicing / regulation of alternative mRNA splicing, via spliceosome / negative regulation of telomere maintenance via telomerase / regulation of RNA splicing / SARS-CoV-1 modulates host translation machinery / Processing of Capped Intron-Containing Pre-mRNA / mRNA transport / cellular response to glucose starvation / positive regulation of telomere maintenance via telomerase / catalytic step 2 spliceosome / mRNA Splicing - Major Pathway / spliceosomal complex / mRNA splicing, via spliceosome / single-stranded DNA binding / single-stranded RNA binding / ribonucleoprotein complex / protein domain specific binding / synapse / DNA binding / RNA binding / extracellular exosome / nucleoplasm / identical protein binding / nucleus / membrane / cytoplasm / cytosol Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.75 Å | |||||||||
Authors | Dunnett, L. / Prischi, F. | |||||||||
| Funding support | 1items
| |||||||||
Citation | Journal: J.Biol.Chem. / Year: 2025Title: Enhanced identification of small molecules binding to hnRNPA1 via cryptic pockets mapping coupled with X-ray fragment screening. Authors: Dunnett, L. / Das, S. / Venditti, V. / Prischi, F. #1: Journal: Biorxiv / Year: 2024 Title: Enhanced identification of small molecules binding to hnRNPA1 via cryptic pockets mapping coupled with X-Ray fragment screening. Authors: Dunnett, L. / Das, S. / Venditti, V. / Prischi, F. | |||||||||
| History |
|
-
Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
|---|
-
Downloads & links
-
Download
| PDBx/mmCIF format | 9hql.cif.gz | 57.9 KB | Display | PDBx/mmCIF format |
|---|---|---|---|---|
| PDB format | pdb9hql.ent.gz | 35.8 KB | Display | PDB format |
| PDBx/mmJSON format | 9hql.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9hql_validation.pdf.gz | 734.5 KB | Display | wwPDB validaton report |
|---|---|---|---|---|
| Full document | 9hql_full_validation.pdf.gz | 734.9 KB | Display | |
| Data in XML | 9hql_validation.xml.gz | 12.2 KB | Display | |
| Data in CIF | 9hql_validation.cif.gz | 16.9 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/hq/9hql ftp://data.pdbj.org/pub/pdb/validation_reports/hq/9hql | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9f4dC ![]() 9f4gC ![]() 9f4hC ![]() 9f4jC ![]() 9f4kC ![]() 9f4lC ![]() 9f4nC ![]() 9f4oC ![]() 9f4pC ![]() 9f4qC ![]() 9f4rC ![]() 9f4sC ![]() 9f4tC ![]() 9f4uC ![]() 9f4vC ![]() 9f4wC ![]() 9f4xC ![]() 9f4yC ![]() 9f4zC ![]() 9f50C ![]() 9f51C ![]() 9f52C ![]() 9f53C ![]() 9f54C ![]() 9f55C ![]() 9f5cC ![]() 9f5dC ![]() 9f5eC ![]() 9f5fC ![]() 9f5gC ![]() 9f5kC ![]() 9f7fC ![]() 9f7hC ![]() 9hq9C ![]() 9hqjC C: citing same article ( |
|---|---|
| Similar structure data | Similarity search - Function & homology F&H Search |
-
Links
-
Assembly
| Deposited unit | ![]()
| ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 |
| ||||||||||||
| Unit cell |
|
-
Components
| #1: Protein | Mass: 22357.109 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HNRNPA1, HNRPA1 / Production host: ![]() |
|---|---|
| #2: Chemical | ChemComp-VZM / |
| #3: Water | ChemComp-HOH / |
| Has ligand of interest | Y |
| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
|---|
-
Sample preparation
| Crystal | Density Matthews: 2.06 Å3/Da / Density % sol: 40.34 % |
|---|---|
| Crystal grow | Temperature: 289 K / Method: vapor diffusion, sitting drop / pH: 8.5 Details: 0.1 M Tris-HCl, pH 8.50, 25% PEG-4000, 8% 2-Methyl-2,4-pentanediol |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
|---|---|
| Diffraction source | Source: SYNCHROTRON / Site: Diamond / Beamline: I04-1 / Wavelength: 0.91587 Å |
| Detector | Type: DECTRIS PILATUS 6M-F / Detector: PIXEL / Date: Jun 29, 2018 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.91587 Å / Relative weight: 1 |
| Reflection | Resolution: 1.75→55.59 Å / Num. obs: 17906 / % possible obs: 96.6 % / Redundancy: 1.8 % / Biso Wilson estimate: 18.38 Å2 / CC1/2: 0.981 / Rmerge(I) obs: 0.092 / Net I/σ(I): 11.1 |
| Reflection shell | Resolution: 1.75→1.78 Å / Mean I/σ(I) obs: 2.5 / Num. unique obs: 950 / CC1/2: 0.767 / % possible all: 95.8 |
-
Processing
| Software |
| |||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.75→55.59 Å / SU ML: 0.2337 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 22.6323 Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
| |||||||||||||||||||||||||||||||||||||||||||||||||
| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 21.17 Å2 | |||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.75→55.59 Å
| |||||||||||||||||||||||||||||||||||||||||||||||||
| Refine LS restraints |
| |||||||||||||||||||||||||||||||||||||||||||||||||
| LS refinement shell |
|
Movie
Controller
About Yorodumi




Homo sapiens (human)
X-RAY DIFFRACTION
Citation


































PDBj






