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Yorodumi- PDB-1fs1: INSIGHTS INTO SCF UBIQUITIN LIGASES FROM THE STRUCTURE OF THE SKP... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 1fs1 | ||||||
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| Title | INSIGHTS INTO SCF UBIQUITIN LIGASES FROM THE STRUCTURE OF THE SKP1-SKP2 COMPLEX | ||||||
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Keywords | LIGASE / Skp1 / Skp2 / F-box / LRR / leucine-rich repeat / SCF / ubiquitin / E3 / ubiquitin protein ligase | ||||||
| Function / homology | Function and homology informationpositive regulation of protein polyubiquitination / F-box domain binding / cellular response to cell-matrix adhesion / Aberrant regulation of mitotic exit in cancer due to RB1 defects / PcG protein complex / positive regulation of ubiquitin protein ligase activity / Cul7-RING ubiquitin ligase complex / Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling / maintenance of protein location in nucleus / SCF ubiquitin ligase complex ...positive regulation of protein polyubiquitination / F-box domain binding / cellular response to cell-matrix adhesion / Aberrant regulation of mitotic exit in cancer due to RB1 defects / PcG protein complex / positive regulation of ubiquitin protein ligase activity / Cul7-RING ubiquitin ligase complex / Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling / maintenance of protein location in nucleus / SCF ubiquitin ligase complex / SCF-dependent proteasomal ubiquitin-dependent protein catabolic process / positive regulation of intracellular estrogen receptor signaling pathway / ubiquitin ligase complex scaffold activity / Prolactin receptor signaling / cullin family protein binding / protein K63-linked ubiquitination / protein monoubiquitination / ubiquitin-like ligase-substrate adaptor activity / protein K48-linked ubiquitination / positive regulation of double-strand break repair via homologous recombination / Nuclear events stimulated by ALK signaling in cancer / positive regulation of smooth muscle cell proliferation / Regulation of BACH1 activity / molecular function activator activity / MAP3K8 (TPL2)-dependent MAPK1/3 activation / SCF-beta-TrCP mediated degradation of Emi1 / NIK-->noncanonical NF-kB signaling / Vpu mediated degradation of CD4 / Dectin-1 mediated noncanonical NF-kB signaling / Activation of NF-kappaB in B cells / Degradation of GLI1 by the proteasome / Iron uptake and transport / GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 / Negative regulation of NOTCH4 signaling / G1/S transition of mitotic cell cycle / Degradation of GLI2 by the proteasome / GLI3 is processed to GLI3R by the proteasome / FBXL7 down-regulates AURKA during mitotic entry and in early mitosis / APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 / Degradation of beta-catenin by the destruction complex / beta-catenin binding / NOTCH1 Intracellular Domain Regulates Transcription / CLEC7A (Dectin-1) signaling / SCF(Skp2)-mediated degradation of p27/p21 / Constitutive Signaling by NOTCH1 PEST Domain Mutants / Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants / FCERI mediated NF-kB activation / G2/M transition of mitotic cell cycle / Interleukin-1 signaling / Orc1 removal from chromatin / protein polyubiquitination / Regulation of RUNX2 expression and activity / Cyclin D associated events in G1 / : / Regulation of PLK1 Activity at G2/M Transition / Downstream TCR signaling / Antigen processing: Ubiquitination & Proteasome degradation / Neddylation / regulation of apoptotic process / defense response to virus / proteasome-mediated ubiquitin-dependent protein catabolic process / regulation of cell cycle / Ub-specific processing proteases / protein ubiquitination / chromatin remodeling / protein domain specific binding / innate immune response / centrosome / nucleolus / nucleoplasm / identical protein binding / nucleus / cytoplasm / cytosol Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / Resolution: 1.8 Å | ||||||
Authors | Schulman, B.A. / Carrano, A.C. / Jeffrey, P.D. / Bowen, Z. / Kinnucan, E.R.E. / Finnin, M.S. / Elledge, S.J. / Harper, J.W. / Pagano, M. / Pavletich, N.P. | ||||||
Citation | Journal: Nature / Year: 2000Title: Insights into SCF ubiquitin ligases from the structure of the Skp1-Skp2 complex. Authors: Schulman, B.A. / Carrano, A.C. / Jeffrey, P.D. / Bowen, Z. / Kinnucan, E.R. / Finnin, M.S. / Elledge, S.J. / Harper, J.W. / Pagano, M. / Pavletich, N.P. | ||||||
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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 | 1fs1.cif.gz | 88 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1fs1.ent.gz | 66.2 KB | Display | PDB format |
| PDBx/mmJSON format | 1fs1.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1fs1_validation.pdf.gz | 393.2 KB | Display | wwPDB validaton report |
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| Full document | 1fs1_full_validation.pdf.gz | 416.6 KB | Display | |
| Data in XML | 1fs1_validation.xml.gz | 12.1 KB | Display | |
| Data in CIF | 1fs1_validation.cif.gz | 20.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/fs/1fs1 ftp://data.pdbj.org/pub/pdb/validation_reports/fs/1fs1 | HTTPS FTP |
-Related 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: 6105.007 Da / Num. of mol.: 2 / Fragment: RESIDUES 101-153 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() #2: Protein | Mass: 16013.290 Da / Num. of mol.: 2 / Fragment: RESIDUES 1-147 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() #3: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 1.9 Å3/Da / Density % sol: 35.41 % | |||||||||||||||||||||||||
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| Crystal grow | Temperature: 277 K / Method: vapor diffusion, hanging drop / pH: 4.6 Details: PEG 1500, sodium acetate, ammonium acetate, DTT, pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 277K | |||||||||||||||||||||||||
| Crystal grow | *PLUS Temperature: 25 ℃ | |||||||||||||||||||||||||
| Components of the solutions | *PLUS
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-Data collection
| Diffraction source | Source: SYNCHROTRON / Site: NSLS / Beamline: X9A / Wavelength: 1.072 |
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| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.072 Å / Relative weight: 1 |
| Reflection | *PLUS Highest resolution: 1.8 Å / Num. obs: 29068 / % possible obs: 84.4 % / Num. measured all: 206639 / Rmerge(I) obs: 0.037 |
| Reflection shell | *PLUS % possible obs: 47.1 % / Rmerge(I) obs: 0.124 / Mean I/σ(I) obs: 6.7 |
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Processing
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| Refinement | Resolution: 1.8→8 Å / Rfactor Rfree: 0.274 / Rfactor Rwork: 0.218 / σ(F): 0 | ||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.8→8 Å
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| Software | *PLUS Name: CNS / Classification: refinement | ||||||||||||||||||||||||||||||
| Refine LS restraints | *PLUS
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| LS refinement shell | *PLUS Rfactor Rfree: 0.343 / Rfactor Rwork: 0.286 |
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Homo sapiens (human)
X-RAY DIFFRACTION
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