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Yorodumi- PDB-7axs: Structural characterisation of WDR5:CS-VIP8 interaction in cis state 1 -
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Open data
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Basic information
| Entry | Database: PDB / ID: 7axs | |||||||||||||||
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| Title | Structural characterisation of WDR5:CS-VIP8 interaction in cis state 1 | |||||||||||||||
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Keywords | TRANSFERASE / WDR5 / cyclic strained visible-light photoswitches / MLL1 complex disruption / inhibition of hematopoiesis | |||||||||||||||
| Function / homology | Function and homology informationhistone H3Q5ser reader activity / histone H3K4me1 reader activity / Epigenetic regulation of gene expression by MLL3 and MLL4 complexes / MLL3/4 complex / Set1C/COMPASS complex / MLL1/2 complex / ATAC complex / NSL complex / histone H3K4 methyltransferase activity / Cardiogenesis ...histone H3Q5ser reader activity / histone H3K4me1 reader activity / Epigenetic regulation of gene expression by MLL3 and MLL4 complexes / MLL3/4 complex / Set1C/COMPASS complex / MLL1/2 complex / ATAC complex / NSL complex / histone H3K4 methyltransferase activity / Cardiogenesis / Formation of WDR5-containing histone-modifying complexes / histone methyltransferase complex / regulation of cell division / MLL1 complex / regulation of embryonic development / histone acetyltransferase complex / positive regulation of gluconeogenesis / transcription initiation-coupled chromatin remodeling / gluconeogenesis / skeletal system development / RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function / PKMTs methylate histone lysines / RMTs methylate histone arginines / Activation of anterior HOX genes in hindbrain development during early embryogenesis / mitotic spindle / Neddylation / HATs acetylate histones / MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis / histone binding / regulation of cell cycle / regulation of DNA-templated transcription / regulation of transcription by RNA polymerase II / positive regulation of DNA-templated transcription / negative regulation of transcription by RNA polymerase II / nucleoplasm / nucleus Similarity search - Function | |||||||||||||||
| Biological species | Homo sapiens (human) | |||||||||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.88 Å | |||||||||||||||
Authors | Werel, L. / Essen, L.-O. | |||||||||||||||
Citation | Journal: Acs Cent.Sci. / Year: 2022Title: Bistable Photoswitch Allows in Vivo Control of Hematopoiesis. Authors: Albert, L. / Nagpal, J. / Steinchen, W. / Zhang, L. / Werel, L. / Djokovic, N. / Ruzic, D. / Hoffarth, M. / Xu, J. / Kaspareit, J. / Abendroth, F. / Royant, A. / Bange, G. / Nikolic, K. / ...Authors: Albert, L. / Nagpal, J. / Steinchen, W. / Zhang, L. / Werel, L. / Djokovic, N. / Ruzic, D. / Hoffarth, M. / Xu, J. / Kaspareit, J. / Abendroth, F. / Royant, A. / Bange, G. / Nikolic, K. / Ryu, S. / Dou, Y. / Essen, L.O. / Vazquez, O. | |||||||||||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 7axs.cif.gz | 143.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7axs.ent.gz | 110.2 KB | Display | PDB format |
| PDBx/mmJSON format | 7axs.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7axs_validation.pdf.gz | 439.5 KB | Display | wwPDB validaton report |
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| Full document | 7axs_full_validation.pdf.gz | 443.4 KB | Display | |
| Data in XML | 7axs_validation.xml.gz | 17.1 KB | Display | |
| Data in CIF | 7axs_validation.cif.gz | 25.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ax/7axs ftp://data.pdbj.org/pub/pdb/validation_reports/ax/7axs | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7axpC ![]() 7axqC ![]() 7axuC ![]() 7axxC ![]() 6iamS C: citing same article ( S: Starting model for refinement |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 |
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| Unit cell |
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Components
| #1: Protein | Mass: 36635.438 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: WDR5, component of MLL1 methyltransferase complex, chromatin regulator Source: (gene. exp.) Homo sapiens (human) / Gene: WDR5, BIG3 / Production host: ![]() |
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| #2: Protein/peptide | Mass: 943.966 Da / Num. of mol.: 1 / Source method: obtained synthetically Details: cyclic peptide, cyclic strained visible-light photoswitch, WDR5-binder, disrupts MLL1 complex via MLL1-WDR5 inhibition Source: (synth.) Homo sapiens (human) |
| #3: Water | ChemComp-HOH / |
| Has ligand of interest | N |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 1.99 Å3/Da / Density % sol: 38.19 % |
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| Crystal grow | Temperature: 277.15 K / Method: vapor diffusion, sitting drop / pH: 8.5 Details: 10% (w/v) PEG20000, 20% (v/v) PEG550 MME, 0.02 M sodium formate, 0.02 M ammonium acetate, 0.02 M trisodium citrate, 0.02 M sodium potassium L-tartrate, 0.02 M sodium oxamate |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: SLS / Beamline: X06SA / Wavelength: 1 Å |
| Detector | Type: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Aug 19, 2019 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 1.88→44.51 Å / Num. obs: 22302 / % possible obs: 89.52 % / Redundancy: 1.9 % / Biso Wilson estimate: 21.76 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.02852 / Rpim(I) all: 0.02852 / Rrim(I) all: 0.04034 / Net I/σ(I): 13.12 |
| Reflection shell | Resolution: 1.88→1.948 Å / Redundancy: 1.9 % / Rmerge(I) obs: 0.2242 / Mean I/σ(I) obs: 2.78 / Num. unique obs: 3521 / CC1/2: 0.894 / Rpim(I) all: 0.2242 / Rrim(I) all: 0.3171 / % possible all: 77.66 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 6IAM Resolution: 1.88→44.468 Å / SU ML: 0.2 / Cross valid method: THROUGHOUT / σ(F): 1.35 / Phase error: 22.97 / Stereochemistry target values: ML
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso max: 89.33 Å2 / Biso mean: 24.978 Å2 / Biso min: 11.92 Å2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: final / Resolution: 1.88→44.468 Å
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| LS refinement shell | Refine-ID: X-RAY DIFFRACTION / Rfactor Rfree error: 0
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| Refinement TLS params. | Method: refined / Refine-ID: X-RAY DIFFRACTION
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| Refinement TLS group |
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Homo sapiens (human)
X-RAY DIFFRACTION
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