[English] 日本語
Yorodumi
- PDB-7sxh: BIO-8546 bound GSK3beta-axin complex -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 7sxh
TitleBIO-8546 bound GSK3beta-axin complex
Components
  • Glycogen synthase kinase-3 beta
  • axin peptide
KeywordsHYDROLASE / kinase
Function / homology
Function and homology information


regulation of microtubule anchoring at centrosome / negative regulation of glycogen (starch) synthase activity / neuron projection organization / negative regulation of mesenchymal stem cell differentiation / beta-catenin destruction complex disassembly / negative regulation of type B pancreatic cell development / superior temporal gyrus development / positive regulation of protein localization to cilium / negative regulation of glycogen biosynthetic process / negative regulation of dopaminergic neuron differentiation ...regulation of microtubule anchoring at centrosome / negative regulation of glycogen (starch) synthase activity / neuron projection organization / negative regulation of mesenchymal stem cell differentiation / beta-catenin destruction complex disassembly / negative regulation of type B pancreatic cell development / superior temporal gyrus development / positive regulation of protein localization to cilium / negative regulation of glycogen biosynthetic process / negative regulation of dopaminergic neuron differentiation / maintenance of cell polarity / positive regulation of protein localization to centrosome / : / positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway / positive regulation of cilium assembly / negative regulation of protein acetylation / APC truncation mutants have impaired AXIN binding / AXIN missense mutants destabilize the destruction complex / Truncations of AMER1 destabilize the destruction complex / beta-catenin destruction complex / tau-protein kinase / CRMPs in Sema3A signaling / heart valve development / regulation of microtubule-based process / regulation of protein export from nucleus / Beta-catenin phosphorylation cascade / Signaling by GSK3beta mutants / CTNNB1 S33 mutants aren't phosphorylated / CTNNB1 S37 mutants aren't phosphorylated / CTNNB1 S45 mutants aren't phosphorylated / CTNNB1 T41 mutants aren't phosphorylated / Maturation of nucleoprotein / cellular response to interleukin-3 / Wnt signalosome / negative regulation of protein localization to nucleus / negative regulation of TOR signaling / regulation of long-term synaptic potentiation / Disassembly of the destruction complex and recruitment of AXIN to the membrane / Maturation of nucleoprotein / AKT phosphorylates targets in the cytosol / negative regulation of calcineurin-NFAT signaling cascade / positive regulation of cell-matrix adhesion / regulation of axon extension / G protein-coupled dopamine receptor signaling pathway / negative regulation of phosphoprotein phosphatase activity / regulation of dendrite morphogenesis / establishment of cell polarity / regulation of axonogenesis / tau-protein kinase activity / glycogen metabolic process / ER overload response / Constitutive Signaling by AKT1 E17K in Cancer / protein kinase A catalytic subunit binding / dynactin binding / NF-kappaB binding / Regulation of HSF1-mediated heat shock response / epithelial to mesenchymal transition / negative regulation of osteoblast differentiation / canonical Wnt signaling pathway / negative regulation of protein-containing complex assembly / positive regulation of autophagy / regulation of microtubule cytoskeleton organization / regulation of cellular response to heat / cellular response to retinoic acid / extrinsic apoptotic signaling pathway / negative regulation of extrinsic apoptotic signaling pathway via death domain receptors / extrinsic apoptotic signaling pathway in absence of ligand / presynaptic modulation of chemical synaptic transmission / negative regulation of insulin receptor signaling pathway / excitatory postsynaptic potential / positive regulation of protein export from nucleus / positive regulation of GTPase activity / positive regulation of protein ubiquitination / Ubiquitin-dependent degradation of Cyclin D / hippocampus development / positive regulation of cell differentiation / GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 / peptidyl-threonine phosphorylation / Degradation of GLI2 by the proteasome / GLI3 is processed to GLI3R by the proteasome / positive regulation of protein-containing complex assembly / Degradation of beta-catenin by the destruction complex / negative regulation of canonical Wnt signaling pathway / tau protein binding / B-WICH complex positively regulates rRNA expression / regulation of circadian rhythm / beta-catenin binding / circadian rhythm / positive regulation of protein catabolic process / cellular response to amyloid-beta / Regulation of RUNX2 expression and activity / neuron projection development / positive regulation of neuron apoptotic process / p53 binding / positive regulation of proteasomal ubiquitin-dependent protein catabolic process / presynapse / positive regulation of protein binding / insulin receptor signaling pathway / negative regulation of neuron projection development / kinase activity
Similarity search - Function
Glycogen synthase kinase 3, catalytic domain / Serine/threonine-protein kinase, active site / Serine/Threonine protein kinases active-site signature. / Protein kinase domain / Serine/Threonine protein kinases, catalytic domain / Protein kinase, ATP binding site / Protein kinases ATP-binding region signature. / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily
Similarity search - Domain/homology
Chem-D1E / Glycogen synthase kinase-3 beta
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.09 Å
AuthorsChodaparambil, J.V.
Funding support1items
OrganizationGrant numberCountry
Other private
CitationJournal: Acs Chem Neurosci / Year: 2023
Title: Elucidation of the GSK3 alpha Structure Informs the Design of Novel, Paralog-Selective Inhibitors.
Authors: Amaral, B. / Capacci, A. / Anderson, T. / Tezer, C. / Bajrami, B. / Lulla, M. / Lucas, B. / Chodaparambil, J.V. / Marcotte, D. / Kumar, P.R. / Murugan, P. / Spilker, K. / Cullivan, M. / ...Authors: Amaral, B. / Capacci, A. / Anderson, T. / Tezer, C. / Bajrami, B. / Lulla, M. / Lucas, B. / Chodaparambil, J.V. / Marcotte, D. / Kumar, P.R. / Murugan, P. / Spilker, K. / Cullivan, M. / Wang, T. / Peterson, A.C. / Enyedy, I. / Ma, B. / Chen, T. / Yousaf, Z. / Calhoun, M. / Golonzhka, O. / Dillon, G.M. / Koirala, S.
History
DepositionNov 23, 2021Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jun 14, 2023Provider: repository / Type: Initial release
Revision 1.1Oct 25, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model
Revision 1.2Nov 15, 2023Group: Data collection / Category: chem_comp_atom / chem_comp_bond / Item: _chem_comp_atom.atom_id / _chem_comp_bond.atom_id_2

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Glycogen synthase kinase-3 beta
B: axin peptide
hetero molecules


Theoretical massNumber of molelcules
Total (without water)41,9313
Polymers41,4652
Non-polymers4671
Water2,234124
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1250 Å2
ΔGint-15 kcal/mol
Surface area16270 Å2
MethodPISA
Unit cell
Length a, b, c (Å)68.610, 72.640, 79.790
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number19
Space group name H-MP212121
Space group name HallP2ac2ab
Symmetry operation#1: x,y,z
#2: x+1/2,-y+1/2,-z
#3: -x,y+1/2,-z+1/2
#4: -x+1/2,-y,z+1/2

-
Components

#1: Protein Glycogen synthase kinase-3 beta / GSK-3 beta / Serine/threonine-protein kinase GSK3B


Mass: 39553.359 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: GSK3B / Production host: Spodoptera frugiperda (fall armyworm)
References: UniProt: P49841, tau-protein kinase, non-specific serine/threonine protein kinase
#2: Protein/peptide axin peptide


Mass: 1911.183 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human)
#3: Chemical ChemComp-D1E / (4S,5R,8R)-4-ethyl-8-fluoro-4-[3-(3-fluoro-5-methoxypyridin-4-yl)phenyl]-7,7-dimethyl-4,5,6,7,8,9-hexahydro-2H-pyrazolo[3,4-b]quinolin-5-ol


Mass: 466.523 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C26H28F2N4O2 / Feature type: SUBJECT OF INVESTIGATION
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 124 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestY

-
Experimental details

-
Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

-
Sample preparation

CrystalDensity Matthews: 2.43 Å3/Da / Density % sol: 49.46 %
Crystal growTemperature: 289 K / Method: vapor diffusion, sitting drop
Details: 0.2M calcium acetate, 0.1M BisTRIS pH 7.0, 5% Glycerol and 17% PEG3350

-
Data collection

DiffractionMean temperature: 93 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SLS / Beamline: X06SA / Wavelength: 0.97 Å
DetectorType: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Feb 3, 2019
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97 Å / Relative weight: 1
ReflectionResolution: 2.09→42.29 Å / Num. obs: 23943 / % possible obs: 99.3 % / Redundancy: 6.5 % / Biso Wilson estimate: 46.51 Å2 / CC1/2: 0.99 / Net I/σ(I): 14.65
Reflection shellResolution: 2.09→2.17 Å / Num. unique obs: 2242 / CC1/2: 0.6

-
Processing

Software
NameVersionClassification
PHENIX1.19.2_4158refinement
XDSdata reduction
Aimlessdata scaling
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 5kpl
Resolution: 2.09→42.29 Å / SU ML: 0.3169 / Cross valid method: FREE R-VALUE / σ(F): 1.35 / Phase error: 30.3707
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.2554 1196 5 %
Rwork0.2138 22722 -
obs0.2159 23918 99.33 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 57.64 Å2
Refinement stepCycle: LAST / Resolution: 2.09→42.29 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2773 0 34 124 2931
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00332897
X-RAY DIFFRACTIONf_angle_d0.96523969
X-RAY DIFFRACTIONf_chiral_restr0.1223454
X-RAY DIFFRACTIONf_plane_restr0.0054508
X-RAY DIFFRACTIONf_dihedral_angle_d6.2163409
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.09-2.180.38581260.32612386X-RAY DIFFRACTION95.55
2.18-2.280.39251310.29122509X-RAY DIFFRACTION99.89
2.28-2.40.33251320.2742497X-RAY DIFFRACTION99.85
2.4-2.550.27281320.2552497X-RAY DIFFRACTION99.7
2.55-2.750.31571300.26152498X-RAY DIFFRACTION99.66
2.75-3.020.29831340.25072536X-RAY DIFFRACTION99.85
3.02-3.460.28471340.23422552X-RAY DIFFRACTION99.89
3.46-4.360.21141350.18112556X-RAY DIFFRACTION99.81
4.36-42.290.21571420.18052691X-RAY DIFFRACTION99.75
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
12.94734220193-1.503735839514.499826045463.45033077418-0.8794421639488.73038866205-0.1152638438450.1700184922380.3421628296630.05318971794070.3706713953190.19494318425-0.3361720247150.286375197292-0.04025213337570.455848125883-0.0345374701337-0.02727137296570.587700960736-0.02628262692260.64464396565423.18331266958.3523033062517.6285769186
27.25197445519-1.02062122173-2.420731134642.11920518321-0.1453961666396.47789166445-0.4112904596790.238655768086-0.01678128814380.3186790144510.22615116825-0.4172869078940.2247793945920.2232576252420.08110548618160.442077172982-0.0311256152102-0.0318217950330.338806535226-0.04743606998380.4575519497316.2556941758.5288849489518.6937644806
38.668296641683.145754817784.097041689594.118890268533.93290673837.46854981575-0.0878654993992-0.1318620335660.0701294828248-0.114661760420.278155048174-0.46614618151-0.4445301398020.481225227218-0.2422475404860.3456289181740.00197976288056-0.02457484648790.3753472557350.007923708506840.40873006836817.01905257456.0307285668518.6464232155
42.923467299880.02298767121320.1443831001043.087800410692.205507057345.68700222515-0.0408485609140.3812169793070.324322551534-0.3697448568590.166363906014-0.174315975957-0.3476200001860.3925811453230.0271463561470.369030068658-0.04963911504680.01767772515940.3945287987150.04155295572970.4002333397325.11941244529-0.07745151451662.85408645872
54.212272826-0.845525835244-2.200209681742.952016264641.278724207768.495722769280.190426176866-0.6508728928460.7448030216250.171321998130.07136656318640.18275011274-0.8195176548-0.257311754938-0.2214800811070.6127092761040.01443009656420.0886792472490.530038195332-0.05455303163320.613983204872-3.086282206077.8017015103818.9157559861
65.31235762415-1.37971507686-1.565751586023.539618264510.7184009382763.343084734290.2355469188540.3627836281110.808646129622-0.23917011247-0.04319664101980.459018600775-0.569695008922-0.431326632014-0.2428408647310.4353941901870.0399317396610.006217869225420.4118967355930.08006261173950.6411924917-10.17658019997.487697745935.53896743598
77.1285358844-0.285606273607-1.093891609416.56408552321.232647967586.721255770140.01706703280470.03227081804520.7412118158120.324783781902-0.45399390851.3031985281-0.599509465325-1.63364129492-0.09800660725320.4551175429230.0766850266840.06322281152920.6723847843350.01460673747240.918936887353-24.64116113056.922504925219.35297441332
85.63897695577-1.505744851560.2206327274815.06798254738-0.4034405845956.54257743775-0.05821121245991.21059980692-0.0099135594896-0.397331866751-0.2538845893730.4576377120940.217240650693-0.778324812413-0.07233619259580.409452133469-0.033063857033-0.07769668754260.5904173390710.008627054565830.478483994985-11.5272196164-4.56409360241-4.52351641316
93.35978816265-1.44238841991-0.3306583759254.35547850836-0.2415859930474.08479794190.004916533414830.173918443085-0.431485331354-0.118616530632-0.1257898862970.00102697153850.7747911480740.3054209011170.1381796099720.541982244273-0.02442506942930.009390491985070.3564293903030.008123795557090.410738839872-0.205022597027-13.74082959465.44056059005
107.399514395861.61463167756.377605130526.1337135761-1.075338287638.87890476857-0.156986007763-0.3121473035081.87857817704-1.4903547534-0.403078842814-0.127805511593-2.03534561598-0.9892139100380.08307171493270.9613349986090.2382713921130.0337342780020.6793341371850.04326604230831.76380769041-23.431728612418.41276483286.34022665348
Refinement TLS group

Refine-ID: X-RAY DIFFRACTION

IDRefine TLS-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11chain 'A' and (resid 37 through 67 )AA37 - 671 - 31
22chain 'A' and (resid 68 through 103 )AA68 - 10332 - 67
33chain 'A' and (resid 104 through 133 )AA104 - 13368 - 94
44chain 'A' and (resid 134 through 198 )AA134 - 19895 - 157
55chain 'A' and (resid 199 through 219 )AA199 - 219158 - 178
66chain 'A' and (resid 220 through 273 )AA220 - 273179 - 232
77chain 'A' and (resid 274 through 300 )AA274 - 300233 - 258
88chain 'A' and (resid 301 through 320 )AA301 - 320259 - 278
99chain 'A' and (resid 321 through 383 )AA321 - 383279 - 341
1010chain 'B' and (resid 385 through 400 )BC385 - 4001 - 16

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbjlvh1.pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more