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Open data
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Basic information
Entry | Database: PDB / ID: 5aiu | ||||||
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Title | A complex of RNF4-RING domain, Ubc13-Ub (isopeptide crosslink) | ||||||
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![]() | LIGASE/SIGNALING PROTEIN / LIGASE-SIGNALING PROTEIN COMPLEX / COMPLEX / FUSION PROTEIN | ||||||
Function / homology | ![]() regulation of spindle assembly / regulation of kinetochore assembly / SUMO polymer binding / Antigen processing: Ubiquitination & Proteasome degradation / : / UBC13-MMS2 complex / response to human chorionic gonadotropin / ubiquitin conjugating enzyme complex / ubiquitin-protein transferase activator activity / positive regulation of protein K63-linked ubiquitination ...regulation of spindle assembly / regulation of kinetochore assembly / SUMO polymer binding / Antigen processing: Ubiquitination & Proteasome degradation / : / UBC13-MMS2 complex / response to human chorionic gonadotropin / ubiquitin conjugating enzyme complex / ubiquitin-protein transferase activator activity / positive regulation of protein K63-linked ubiquitination / DNA double-strand break processing / cellular response to hydroxyurea / cellular response to arsenic-containing substance / protein K6-linked ubiquitination / cellular response to testosterone stimulus / protein K11-linked ubiquitination / response to arsenic-containing substance / ubiquitin conjugating enzyme binding / postreplication repair / negative regulation of protein localization to chromatin / positive regulation of double-strand break repair / positive regulation of intracellular signal transduction / nuclear androgen receptor binding / E2 ubiquitin-conjugating enzyme / cellular response to cytokine stimulus / ubiquitin conjugating enzyme activity / protein K63-linked ubiquitination / antiviral innate immune response / protein autoubiquitination / protein K48-linked ubiquitination / regulation of DNA repair / ubiquitin ligase complex / nucleosome binding / Maturation of protein E / Maturation of protein E / ER Quality Control Compartment (ERQC) / Myoclonic epilepsy of Lafora / FLT3 signaling by CBL mutants / Prevention of phagosomal-lysosomal fusion / IRAK2 mediated activation of TAK1 complex / negative regulation of TORC1 signaling / Alpha-protein kinase 1 signaling pathway / Glycogen synthesis / IRAK1 recruits IKK complex / IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation / Membrane binding and targetting of GAG proteins / Endosomal Sorting Complex Required For Transport (ESCRT) / IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation / PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 / Negative regulation of FLT3 / Constitutive Signaling by NOTCH1 HD Domain Mutants / Regulation of FZD by ubiquitination / TICAM1,TRAF6-dependent induction of TAK1 complex / NOTCH2 Activation and Transmission of Signal to the Nucleus / TICAM1-dependent activation of IRF3/IRF7 / APC/C:Cdc20 mediated degradation of Cyclin B / p75NTR recruits signalling complexes / positive regulation of DNA repair / Downregulation of ERBB4 signaling / APC-Cdc20 mediated degradation of Nek2A / PINK1-PRKN Mediated Mitophagy / TBP-class protein binding / TRAF6-mediated induction of TAK1 complex within TLR4 complex / TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling / Pexophagy / Regulation of innate immune responses to cytosolic DNA / InlA-mediated entry of Listeria monocytogenes into host cells / VLDLR internalisation and degradation / Downregulation of ERBB2:ERBB3 signaling / NF-kB is activated and signals survival / NRIF signals cell death from the nucleus / Regulation of PTEN localization / Activated NOTCH1 Transmits Signal to the Nucleus / Regulation of BACH1 activity / Translesion synthesis by REV1 / Synthesis of active ubiquitin: roles of E1 and E2 enzymes / Translesion synthesis by POLK / MAP3K8 (TPL2)-dependent MAPK1/3 activation / TICAM1, RIP1-mediated IKK complex recruitment / Downregulation of TGF-beta receptor signaling / Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) / Translesion synthesis by POLI / Gap-filling DNA repair synthesis and ligation in GG-NER / Josephin domain DUBs / Regulation of activated PAK-2p34 by proteasome mediated degradation / InlB-mediated entry of Listeria monocytogenes into host cell / IKK complex recruitment mediated by RIP1 / JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 / TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) / N-glycan trimming in the ER and Calnexin/Calreticulin cycle / Autodegradation of Cdh1 by Cdh1:APC/C / TNFR1-induced NF-kappa-B signaling pathway / APC/C:Cdc20 mediated degradation of Securin / ubiquitin binding / Asymmetric localization of PCP proteins / TCF dependent signaling in response to WNT / SCF-beta-TrCP mediated degradation of Emi1 / AUF1 (hnRNP D0) binds and destabilizes mRNA / NIK-->noncanonical NF-kB signaling / Ubiquitin-dependent degradation of Cyclin D Similarity search - Function | ||||||
Biological species | ![]() ![]() ![]() | ||||||
Method | ![]() | ||||||
![]() | Branigan, E. / Naismith, J.H. | ||||||
![]() | ![]() Title: Structural Basis for the Ring Catalyzed Synthesis of K63 Linked Ubiquitin Chains Authors: Branigan, E. / Plechanovova, A. / Jaffray, E. / Naismith, J.H. / Hay, R.T. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 125.9 KB | Display | ![]() |
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PDB format | ![]() | 98.5 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 463.6 KB | Display | ![]() |
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Full document | ![]() | 467.5 KB | Display | |
Data in XML | ![]() | 21.7 KB | Display | |
Data in CIF | ![]() | 29.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
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Assembly
Deposited unit | ![]()
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Unit cell |
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Noncrystallographic symmetry (NCS) | NCS domain:
NCS domain segments: Component-ID: _ / Refine code: _
NCS ensembles :
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Components
-Protein , 3 types, 5 molecules ABECF
#1: Protein | Mass: 14758.155 Da / Num. of mol.: 1 / Fragment: RING DOMAIN, UNP RESIDUES 131-194,131-194 / Mutation: YES Source method: isolated from a genetically manipulated source Details: THE RING DOMAIN IS DUPLICATED BUT AS A FUSED DIMER. THAT IS THE SEQUENCE OF THE RING DOMAIN FROM RNF4 (RESIDUES 131 TO 194) IS LINKED BY A SINGLE GLYCINE RESIDUE TO ANOTHER RING DOMAIN (RESIDUES 131 TO 194). Source: (gene. exp.) ![]() ![]() ![]() ![]() References: UniProt: O88846, Ligases; Forming carbon-nitrogen bonds; Acid-amino-acid ligases (peptide synthases) | ||
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#2: Protein | Mass: 17253.832 Da / Num. of mol.: 2 / Mutation: YES Source method: isolated from a genetically manipulated source Details: CHAIN B COVALENTLY LINKED TO CHAINS C, CHAIN E IS COVALENTLY LINKED TO CHAIN F Source: (gene. exp.) ![]() ![]() ![]() #3: Protein | Mass: 8576.831 Da / Num. of mol.: 2 / Fragment: UNP RESIDUES 1-76 Source method: isolated from a genetically manipulated source Details: CHAIN B COVALENTLY LINKED TO CHAINS C, CHAIN E IS COVALENTLY LINKED TO CHAIN F Source: (gene. exp.) ![]() ![]() ![]() |
-Non-polymers , 3 types, 43 molecules ![](data/chem/img/ZN.gif)
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#4: Chemical | ChemComp-ZN / #5: Chemical | ChemComp-EDO / #6: Water | ChemComp-HOH / | |
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-Details
Sequence details | THIS IS A HEAD TO TAIL FUSION OF TWO RING DOMAINS. THE GAMG AT THE N-TERMINUS IS A CLONING ARTEFACT ...THIS IS A HEAD TO TAIL FUSION OF TWO RING DOMAINS. THE GAMG AT THE N-TERMINUS IS A CLONING ARTEFACT THE ACTIVE SITE C87 HAS BEEN MUTATED TO K87 FOR ATTACHMENT |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.32 Å3/Da / Density % sol: 46.96 % / Description: NONE |
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Crystal grow | Details: 1,2-ETHANEDIOL |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ![]() |
Detector | Type: RIGAKU SATURN / Detector: IMAGE PLATE / Date: Nov 24, 2014 |
Radiation | Monochromator: MIRRORS / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.54178 Å / Relative weight: 1 |
Reflection | Resolution: 2.21→32.2 Å / Num. obs: 29485 / % possible obs: 95 % / Observed criterion σ(I): 0 / Redundancy: 5.7 % / Rmerge(I) obs: 0.06 / Net I/σ(I): 20.9 |
Reflection shell | Resolution: 2.21→2.26 Å / Redundancy: 3.7 % / Rmerge(I) obs: 0.15 / Mean I/σ(I) obs: 7.8 / % possible all: 74.8 |
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Processing
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Refinement | Method to determine structure: OTHER Starting model: NONE Resolution: 2.21→32.02 Å / Cor.coef. Fo:Fc: 0.911 / Cor.coef. Fo:Fc free: 0.89 / SU B: 6.731 / SU ML: 0.172 / Cross valid method: THROUGHOUT / ESU R: 0.328 / ESU R Free: 0.233 / Stereochemistry target values: MAXIMUM LIKELIHOOD Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. U VALUES REFINED INDIVIDUALLY DISORDERED REGIONS WERE MODELED STEREOCHEMICALLY. THE ISOPEPTIDE LINKAGE WAS INCLUDED AS A RESTRAINT.
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Solvent computation | Ion probe radii: 0.85 Å / Shrinkage radii: 0.75 Å / VDW probe radii: 1 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 24.191 Å2
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Refinement step | Cycle: LAST / Resolution: 2.21→32.02 Å
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Refine LS restraints |
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