[English] 日本語
Yorodumi
- PDB-6td2: Mus musculus Acetylcholinesterase in complex with N-(2-(diethylam... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 6td2
TitleMus musculus Acetylcholinesterase in complex with N-(2-(diethylamino)ethyl)-1-(4-(trifluoromethyl)phenyl)methanesulfonamide
ComponentsAcetylcholinesterase
KeywordsHYDROLASE / Complex / Inhibitor
Function / homology
Function and homology information


acetylcholine metabolic process / serine hydrolase activity / choline binding / acetylcholine catabolic process / acetylcholine binding / acetylcholinesterase / acetylcholine receptor signaling pathway / positive regulation of dendrite morphogenesis / osteoblast development / acetylcholinesterase activity ...acetylcholine metabolic process / serine hydrolase activity / choline binding / acetylcholine catabolic process / acetylcholine binding / acetylcholinesterase / acetylcholine receptor signaling pathway / positive regulation of dendrite morphogenesis / osteoblast development / acetylcholinesterase activity / choline metabolic process / positive regulation of axonogenesis / basement membrane / regulation of receptor recycling / side of membrane / synaptic cleft / laminin binding / synapse assembly / collagen binding / response to insulin / neuromuscular junction / receptor internalization / : / retina development in camera-type eye / nuclear envelope / presynaptic membrane / positive regulation of cold-induced thermogenesis / postsynaptic membrane / cell adhesion / endoplasmic reticulum lumen / axon / neuronal cell body / synapse / dendrite / perinuclear region of cytoplasm / Golgi apparatus / cell surface / protein homodimerization activity / extracellular space / identical protein binding / plasma membrane
Similarity search - Function
Acetylcholinesterase, tetramerisation domain / Acetylcholinesterase tetramerisation domain / Cholinesterase / Carboxylesterase type B, conserved site / Carboxylesterases type-B signature 2. / Carboxylesterase type B, active site / Carboxylesterases type-B serine active site. / Carboxylesterase, type B / Carboxylesterase family / Alpha/Beta hydrolase fold
Similarity search - Domain/homology
Chem-ETE / Chem-N2K / Acetylcholinesterase
Similarity search - Component
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / FOURIER SYNTHESIS / Resolution: 2.8 Å
AuthorsForsgren, N. / Ekstrom, F.
Funding support2items
OrganizationGrant numberCountry
Other government
Swedish Research Council
CitationJournal: J.Phys.Chem.B / Year: 2020
Title: Physical Mechanisms Governing Substituent Effects on Arene-Arene Interactions in a Protein Milieu.
Authors: Andersson, C.D. / Mishra, B.K. / Forsgren, N. / Ekstrom, F. / Linusson, A.
History
DepositionNov 7, 2019Deposition site: PDBE / Processing site: PDBE
Revision 1.0Oct 14, 2020Provider: repository / Type: Initial release
Revision 1.1Oct 21, 2020Group: Derived calculations / Category: pdbx_struct_assembly / pdbx_struct_assembly_gen
Revision 1.2Jan 24, 2024Group: Data collection / Database references / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Acetylcholinesterase
B: Acetylcholinesterase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)122,18419
Polymers119,5292
Non-polymers2,65517
Water3,063170
1


  • Idetical with deposited unit
  • defined by author
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)78.957, 111.957, 227.429
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

-
Protein / Sugars , 2 types, 4 molecules AB

#1: Protein Acetylcholinesterase / AChE


Mass: 59764.488 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: Ache / Cell line (production host): HEK293F / Production host: Homo sapiens (human) / References: UniProt: P21836, acetylcholinesterase
#2: Sugar ChemComp-NAG / 2-acetamido-2-deoxy-beta-D-glucopyranose / N-acetyl-beta-D-glucosamine / 2-acetamido-2-deoxy-beta-D-glucose / 2-acetamido-2-deoxy-D-glucose / 2-acetamido-2-deoxy-glucose / N-ACETYL-D-GLUCOSAMINE


Type: D-saccharide, beta linking / Mass: 221.208 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Formula: C8H15NO6
IdentifierTypeProgram
DGlcpNAcbCONDENSED IUPAC CARBOHYDRATE SYMBOLGMML 1.0
N-acetyl-b-D-glucopyranosamineCOMMON NAMEGMML 1.0
b-D-GlcpNAcIUPAC CARBOHYDRATE SYMBOLPDB-CARE 1.0
GlcNAcSNFG CARBOHYDRATE SYMBOLGMML 1.0

-
Non-polymers , 6 types, 185 molecules

#3: Chemical ChemComp-N2K / ~{N}-[2-(diethylamino)ethyl]-1-[4-(trifluoromethyl)phenyl]methanesulfonamide


Mass: 338.389 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C14H21F3N2O2S / Feature type: SUBJECT OF INVESTIGATION
#4: Chemical
ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 6 / Source method: obtained synthetically / Formula: C2H6O2
#5: Chemical
ChemComp-PG0 / 2-(2-METHOXYETHOXY)ETHANOL / PEG 6000


Mass: 120.147 Da / Num. of mol.: 5 / Source method: obtained synthetically / Formula: C5H12O3 / Comment: inhibitor, precipitant*YM
#6: Chemical ChemComp-PE4 / 2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL / POLYETHYLENE GLYCOL PEG4000


Mass: 354.436 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C16H34O8 / Comment: precipitant*YM
#7: Chemical ChemComp-ETE / 2-{2-[2-2-(METHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL


Mass: 208.252 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C9H20O5
#8: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 170 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestY

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 3.68 Å3/Da / Density % sol: 66.6 %
Crystal growTemperature: 277 K / Method: vapor diffusion, hanging drop / pH: 7 / Details: 30 % (w/v) PEG750MME 0.1 M HEPES pH 7.0

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: MAX II / Beamline: I911-5 / Wavelength: 1.041 Å
DetectorType: MARMOSAIC 225 mm CCD / Detector: CCD / Date: Feb 14, 2012
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.041 Å / Relative weight: 1
ReflectionResolution: 2.8→28.9 Å / Num. obs: 50138 / % possible obs: 99.5 % / Redundancy: 3.8 % / Biso Wilson estimate: 45.4038821796 Å2 / Rmerge(I) obs: 0.093 / Net I/σ(I): 13.4
Reflection shellResolution: 2.8→2.95 Å / Rmerge(I) obs: 0.494 / Num. unique obs: 7255

-
Processing

Software
NameVersionClassification
PHENIX1.12_2829refinement
XDSdata reduction
SCALAdata scaling
REFMACphasing
RefinementMethod to determine structure: FOURIER SYNTHESIS
Starting model: 1JO6
Resolution: 2.8→28.851 Å / SU ML: 0.30406205041 / Cross valid method: FREE R-VALUE / σ(F): 1.33784944444 / Phase error: 23.8261974636
RfactorNum. reflection% reflection
Rfree0.215251914175 981 1.96408192684 %
Rwork0.174582101838 --
obs0.175365448692 49947 99.0010108818 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Displacement parametersBiso mean: 51.8911291687 Å2
Refinement stepCycle: LAST / Resolution: 2.8→28.851 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms8327 0 173 170 8670
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.007612529948818823
X-RAY DIFFRACTIONf_angle_d0.99364661748612038
X-RAY DIFFRACTIONf_chiral_restr0.05714342593851285
X-RAY DIFFRACTIONf_plane_restr0.007422598379661572
X-RAY DIFFRACTIONf_dihedral_angle_d11.31840396517094
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.8-2.94750.3099697180511370.2646002301266922X-RAY DIFFRACTION99.6049103993
2.9475-3.1320.2781303885381550.2364302410136906X-RAY DIFFRACTION99.5488509798
3.132-3.37350.2804235142921300.2270553182026974X-RAY DIFFRACTION99.7472620051
3.3735-3.71230.2438139166311440.1777046561077015X-RAY DIFFRACTION99.7075208914
3.7123-4.2480.2220164401611320.1520500976916994X-RAY DIFFRACTION99.3724724585
4.248-5.34650.1436972160761400.1310267288917049X-RAY DIFFRACTION98.8042880704
5.3465-28.850.1779830847451430.1595036646547106X-RAY DIFFRACTION96.3834596463
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)
13.86258575264-1.05555179246-0.590963696831.97264444252-0.939113585985.66248064636-0.265303029985-0.5073841525140.09112250772050.5785119737670.16533128130.0197414764322-0.101832787916-0.07591100440390.009425203457920.452500294194-0.0147966073736-0.03859907229040.277858034952-0.0165003793730.26040528020729.988664734813.059107567941.4656525467
22.619656845430.174222009823-0.4940058471471.58718994098-0.04495931542512.62666029589-0.0806955854521-0.2970295034050.08817655310980.2128885748190.01581858464-0.0591401283954-0.03863762251740.1056674762670.0519865374180.307539624530.0326223038161-0.04109443099330.299746540308-0.0002683948593290.19914010703431.008076624715.901822013127.7083438699
31.751120957310.63267587729-1.226033848592.15731283628-0.7194786978264.94311590548-0.130124637234-0.169507711691-0.2862404635350.0482402309510.0779221347655-0.1305460212710.696579235743-0.03081947351910.05251429200840.3406899619510.0351552919158-0.02094437267820.2611375466160.04648962270270.26849538368532.154781632.9627822573721.1333862563
42.36528459174-0.8944030326512.7480522455.385853565981.592464654488.218972982240.1102440140930.234627919301-0.0376944907215-0.593534506587-0.349459122474-0.921390357480.006975633927141.270389159160.2154178281860.2957225652520.0399327574780.08111085257340.5673344326120.124715663610.43716234914354.03385690813.89551557612.2104914886
53.954535537121.532193499192.319816888974.109723490221.784891505993.64272977727-0.02517663082020.0922659927734-0.269164822444-0.00897910083932-0.0265028623027-0.2318458244060.3922315950260.1793337611340.04243966039480.367356256680.0874925062110.1175665562940.4053238509570.06010694177480.21501082314837.24183373428.010500697149.32667873987
61.93929842115-0.332215306964-0.06165237005921.95812450709-0.7380075738454.10139348027-0.01852442781880.09708063192220.0487649813755-0.127372750790.08340574392760.1957124720560.0685676571734-0.376133602175-0.05585909192160.208936193741-0.0268224485902-0.04058330409860.3217688681560.003582828204620.25406397272919.043303581417.0340637716.23508782144
75.225610529230.2284727712843.905317485798.49293048047-2.037295790014.009895434770.020451867739-0.119994597952-0.6595673253540.2161363364330.3065354532771.09157501570.541466194607-1.18298609541-0.1739802810360.45290078897-0.230409407684-0.006056070925790.5551663562690.08318598864580.5294367709167.069758765831.4045855217413.4499775915
83.08522611664-1.44330815831-5.041837321043.115088733743.245325718928.627803323710.01064256557490.108708309479-0.127703650478-0.4793554977170.02110105466770.2709242375780.0445685320657-0.215346246980.003105477162360.457240940744-0.001459435888-0.1765108637320.6728354830990.06901227892750.3262743909417.65966173916.45479308916-1.30236500891
96.82459455735-1.1689827832-2.964762012032.220226589330.6507038397385.675706269180.06681983884470.7153611464660.0899822632171-0.282248797908-0.175866203240.32626591313-0.00765552201404-1.016272418740.09076255049390.4891443225740.0315744370701-0.09839644842820.495355406795-0.1430855063910.37058180383-3.539175570996.37288373024-62.0030322926
100.769904182377-0.496153303269-0.3077580776032.225450607940.398015405863.321428158870.2108641878790.215085622761-0.130556533907-0.115690686151-0.2230437107550.120578901210.658586249031-0.0726512861586-0.04325991701790.471928830767-0.0429336210747-0.07869744807680.621499991876-0.07447556213850.3023938370135.33430919148-4.03955376657-53.1765683737
112.396797616590.471818943127-0.78109162852.747585828461.02175457712.124049883760.02236499501870.5916937395940.0713905643347-0.389757475879-0.2734641007190.4460143149580.166535944789-0.3088774568880.1976449381630.4490484310970.0794199235199-0.1310435368390.595652112109-0.108540425630.300126263963-1.206560783546.0203862176-53.9495508564
124.95566429622-0.9845068138861.54989064771.680451930120.4738366387481.779118548140.1905277718710.629878412387-0.173477790774-0.114540439748-0.1752946901840.05448539223690.1257906701610.0186597387344-0.03906986573940.398250699614-0.00609301375145-0.02119774272660.420815788564-0.04631175441490.205652774687.55983202143.05520837504-48.9757415155
132.11399680169-1.214421909930.07964298220022.954662776340.7906205291173.050198724370.1079971987820.197425220724-0.04234415473880.006202342476610.0314404851979-0.2622992131410.1713598917760.528037961569-0.1328393963150.3416816146140.0212880461097-0.02167526300320.479759492367-0.04290488430540.24011685655317.27852830254.63149841262-46.6304274886
142.64219304839-2.597841990910.7146935204545.76550018003-2.209882814185.600541154490.0960024765219-0.0813186743227-0.171547018397-0.222207071492-0.0931003193464-0.1462824153580.4093360474740.009298979536590.01151608632840.319356293763-0.0568814357585-0.02342498440840.28382515457-0.07383952396230.2577077823348.565906678164.61410160889-31.6541100656
152.16960347613-0.4290556068440.6506479049731.95778232892-0.1166531392842.533216274440.154764153168-0.328758829671-0.2903258733570.297355706341-0.00540579272354-0.01270748116890.5928723589650.0338600843208-0.1527056363590.537022969672-0.0454360006408-0.03611779161860.403286210872-0.06081079271150.26120680465411.28545599951.31098185872-22.3776939854
161.84693923249-0.9241514225481.114829057075.96171840058-2.604452710435.94519971067-0.0774069382914-0.171032013211-0.06127106696920.2059964903120.1634591023860.4366232978920.186175652242-1.22570057436-0.06039425675980.349012489403-0.0372404358482-0.002784700126340.52400789659-0.132754477530.354762115973-7.493750677627.0100000139-35.5011914127
174.79044156922-0.808314951411.497940132864.99878930898-0.553112456892.233956976060.263918778144-0.4001140281640.7837929829050.4963792826730.01966744466890.736724446919-0.799232840471-0.582385632272-0.2557810888310.5161655166530.07900460313490.07588300987370.521023803543-0.005278922507480.417538891018-1.5603247685622.7729078154-28.9378755548
186.31312068234-0.3226846846395.370742330911.83154385108-0.3319693646354.62775466859-0.1007300042820.17040093337-0.1602900727210.327623976667-0.0935271283641-0.127071018582-0.04363458766140.3485425209190.215839317980.598936068252-0.0543333814620.008495741265280.466001097477-0.008150408801250.20930630369912.739073161611.7700923421-21.7536659898
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resid 1 through 45 )
2X-RAY DIFFRACTION2chain 'A' and (resid 46 through 158 )
3X-RAY DIFFRACTION3chain 'A' and (resid 159 through 240 )
4X-RAY DIFFRACTION4chain 'A' and (resid 241 through 277 )
5X-RAY DIFFRACTION5chain 'A' and (resid 278 through 324 )
6X-RAY DIFFRACTION6chain 'A' and (resid 325 through 486 )
7X-RAY DIFFRACTION7chain 'A' and (resid 487 through 513 )
8X-RAY DIFFRACTION8chain 'A' and (resid 514 through 542 )
9X-RAY DIFFRACTION9chain 'B' and (resid 4 through 45 )
10X-RAY DIFFRACTION10chain 'B' and (resid 46 through 86 )
11X-RAY DIFFRACTION11chain 'B' and (resid 87 through 118 )
12X-RAY DIFFRACTION12chain 'B' and (resid 119 through 170 )
13X-RAY DIFFRACTION13chain 'B' and (resid 171 through 318 )
14X-RAY DIFFRACTION14chain 'B' and (resid 319 through 348 )
15X-RAY DIFFRACTION15chain 'B' and (resid 349 through 440 )
16X-RAY DIFFRACTION16chain 'B' and (resid 441 through 486 )
17X-RAY DIFFRACTION17chain 'B' and (resid 487 through 513 )
18X-RAY DIFFRACTION18chain 'B' and (resid 514 through 542 )

+
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