[English] 日本語
Yorodumi
- PDB-8d6d: Crystal Structure of Human Myt1 Kinase domain Bounded with compound 39 -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8d6d
TitleCrystal Structure of Human Myt1 Kinase domain Bounded with compound 39
ComponentsMembrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
KeywordsSIGNALING PROTEIN / Transferase/Inhibitor / Kinase Inhibitor complex / Transferase-Inhibitor complex
Function / homology
Function and homology information


negative regulation of G2/MI transition of meiotic cell cycle / G2/M DNA replication checkpoint / negative regulation of G2/M transition of mitotic cell cycle / Polo-like kinase mediated events / regulation of mitotic nuclear division / regulation of cyclin-dependent protein serine/threonine kinase activity / Cyclin A/B1/B2 associated events during G2/M transition / meiotic cell cycle / G2/M transition of mitotic cell cycle / kinase activity ...negative regulation of G2/MI transition of meiotic cell cycle / G2/M DNA replication checkpoint / negative regulation of G2/M transition of mitotic cell cycle / Polo-like kinase mediated events / regulation of mitotic nuclear division / regulation of cyclin-dependent protein serine/threonine kinase activity / Cyclin A/B1/B2 associated events during G2/M transition / meiotic cell cycle / G2/M transition of mitotic cell cycle / kinase activity / mitotic cell cycle / protein tyrosine kinase activity / non-specific serine/threonine protein kinase / protein kinase activity / phosphorylation / Golgi membrane / protein serine kinase activity / protein serine/threonine kinase activity / endoplasmic reticulum membrane / nucleolus / Golgi apparatus / endoplasmic reticulum / nucleoplasm / ATP binding / membrane / nucleus / metal ion binding / cytoplasm / cytosol
Similarity search - Function
Tyrosine/threonine-protein kinase, Cdc2 inhibitor / 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-QGY / Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.35 Å
AuthorsPau, V.P.T. / Mao, D.Y.L. / Mader, P. / Orlicky, S. / Sicheri, F.
Funding support Canada, 2items
OrganizationGrant numberCountry
Ontario Research FundRE08-065 Canada
Other private
CitationJournal: J.Med.Chem. / Year: 2022
Title: Discovery of an Orally Bioavailable and Selective PKMYT1 Inhibitor, RP-6306.
Authors: Szychowski, J. / Papp, R. / Dietrich, E. / Liu, B. / Vallee, F. / Leclaire, M.E. / Fourtounis, J. / Martino, G. / Perryman, A.L. / Pau, V. / Yin, S.Y. / Mader, P. / Roulston, A. / Truchon, J. ...Authors: Szychowski, J. / Papp, R. / Dietrich, E. / Liu, B. / Vallee, F. / Leclaire, M.E. / Fourtounis, J. / Martino, G. / Perryman, A.L. / Pau, V. / Yin, S.Y. / Mader, P. / Roulston, A. / Truchon, J.F. / Marshall, C.G. / Diallo, M. / Duffy, N.M. / Stocco, R. / Godbout, C. / Bonneau-Fortin, A. / Kryczka, R. / Bhaskaran, V. / Mao, D. / Orlicky, S. / Beaulieu, P. / Turcotte, P. / Kurinov, I. / Sicheri, F. / Mamane, Y. / Gallant, M. / Black, W.C.
History
DepositionJun 6, 2022Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jul 27, 2022Provider: repository / Type: Initial release
Revision 1.1Aug 10, 2022Group: Database references / Category: citation / citation_author
Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_ASTM / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year / _citation_author.identifier_ORCID / _citation_author.name
Revision 1.2Aug 24, 2022Group: Database references / Category: citation / citation_author
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation_author.identifier_ORCID
Revision 1.3Oct 18, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
B: Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)70,35111
Polymers68,9962
Non-polymers1,3559
Water59433
1
A: Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)35,2076
Polymers34,4981
Non-polymers7095
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
2
B: Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)35,1455
Polymers34,4981
Non-polymers6464
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)51.460, 112.920, 72.660
Angle α, β, γ (deg.)90.000, 110.340, 90.000
Int Tables number4
Space group name H-MP1211
Noncrystallographic symmetry (NCS)NCS domain:
IDEns-IDDetails
11(chain A and (resid 78 through 84 or resid 95...
21(chain B and (resid 78 through 79 or (resid 80...

NCS domain segments:
Dom-IDComponent-IDEns-IDSelection detailsAuth asym-IDAuth seq-ID
111(chain A and (resid 78 through 84 or resid 95...A78 - 84
121(chain A and (resid 78 through 84 or resid 95...A95 - 107
131(chain A and (resid 78 through 84 or resid 95...A108 - 109
141(chain A and (resid 78 through 84 or resid 95...A78 - 361
151(chain A and (resid 78 through 84 or resid 95...A1
211(chain B and (resid 78 through 79 or (resid 80...B78 - 79
221(chain B and (resid 78 through 79 or (resid 80...B80
231(chain B and (resid 78 through 79 or (resid 80...B77 - 361
241(chain B and (resid 78 through 79 or (resid 80...B77 - 361
251(chain B and (resid 78 through 79 or (resid 80...B77 - 361
261(chain B and (resid 78 through 79 or (resid 80...B77 - 361

-
Components

#1: Protein Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase / Myt1 kinase


Mass: 34498.133 Da / Num. of mol.: 2 / Fragment: KINASE DOMAIN, UNP RESIDUES 75-362
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: PKMYT1, MYT1 / Plasmid: pNIC28-Bsa4 / Production host: Escherichia coli (E. coli)
References: UniProt: Q99640, non-specific serine/threonine protein kinase
#2: Chemical
ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 5 / Source method: obtained synthetically / Formula: C2H6O2
#3: Chemical ChemComp-SO4 / SULFATE ION


Mass: 96.063 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: SO4
#4: Chemical ChemComp-QGY / (1P)-2-amino-5-bromo-1-(3-hydroxy-2,6-dimethylphenyl)-1H-pyrrolo[2,3-b]quinoxaline-3-carboxamide


Mass: 426.267 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C19H16BrN5O2 / Feature type: SUBJECT OF INVESTIGATION
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 33 / 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: 2.87 Å3/Da / Density % sol: 57.13 %
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop / pH: 8.25
Details: 5.6 to 6.6% PEG3350, 0.2 M Na2SO4, 0.1 M Tris-HCl and 10% EG
Temp details: 277K for 1 day then 293K for a week

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 24-ID-C / Wavelength: 0.9791 Å
DetectorType: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Sep 3, 2020
RadiationMonochromator: Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9791 Å / Relative weight: 1
ReflectionResolution: 2.35→58.33 Å / Num. obs: 30950 / % possible obs: 94.8 % / Redundancy: 2.651 % / Biso Wilson estimate: 77.15 Å2 / CC1/2: 0.995 / Rmerge(I) obs: 0.064 / Rrim(I) all: 0.08 / Χ2: 0.712 / Net I/σ(I): 6.95 / Num. measured all: 82045
Reflection shell

Diffraction-ID: 1

Resolution (Å)Redundancy (%)Rmerge(I) obsMean I/σ(I) obsNum. measured obsNum. possibleNum. unique obsCC1/2Rrim(I) all% possible all
2.35-2.492.5421.3940.5312400522348790.5041.7593.4
2.49-2.662.6450.7561.0812563490947500.7630.94396.8
2.66-2.872.7650.3962.112486464345160.9460.49297.3
2.87-3.142.7240.1964.1311082423440680.9750.24496.1
3.14-3.512.6180.0928.239523383936380.990.11594.8
3.51-4.062.5510.0613.218070340831640.9940.07492.8
4.06-4.962.7280.05417.687379288127050.9930.06793.9
4.96-6.992.6040.05218.225349223420540.9910.06591.9
6.99-58.332.7150.04720.383193128611760.9920.05891.4

-
Processing

Software
NameVersionClassification
XSCALEdata scaling
PHENIX1.19.2refinement
PDB_EXTRACT3.27data extraction
XDSdata reduction
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 3P1A
Resolution: 2.35→58.33 Å / SU ML: 0.54 / Cross valid method: THROUGHOUT / σ(F): 1.34 / Phase error: 41.47 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.2719 1533 4.99 %
Rwork0.2406 29186 -
obs0.2422 30719 94.79 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso max: 215.83 Å2 / Biso mean: 106.0445 Å2 / Biso min: 57.7 Å2
Refinement stepCycle: final / Resolution: 2.35→58.33 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms3993 0 84 33 4110
Biso mean--97.46 101.99 -
Num. residues----544
Refine LS restraints NCS
Ens-IDDom-IDAuth asym-IDNumberRefine-IDRmsType
11A2338X-RAY DIFFRACTION6.757TORSIONAL
12B2338X-RAY DIFFRACTION6.757TORSIONAL
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Rfactor Rfree error: 0 / Total num. of bins used: 11

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkNum. reflection all% reflection obs (%)
2.35-2.430.52911480.55832585273394
2.43-2.510.54721450.49642620276595
2.51-2.610.44761380.42752697283597
2.61-2.730.41311270.39892733286097
2.73-2.880.48011530.40682694284797
2.88-3.060.40311590.3492667282696
3.06-3.290.31161390.27692659279896
3.29-3.620.2751260.26942632275893
3.62-4.150.24781310.20992623275494
4.15-5.220.21411640.18512614277893
5.23-58.330.2211030.19242662276592
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)
10.8217-0.20051.77521.7851.6022.1427-0.3128-0.01160.2885-0.5783-0.63380.5286-0.1768-0.1473-0.0010.58680.0278-0.1020.7477-0.10451.20149.1203-12.43373.6918
20.4418-0.44031.02440.67810.14330.2211-0.3691-0.05010.28550.3190.0340.46750.27370.1454-0.00020.8902-0.03680.0360.72590.02390.681262.3197-12.253921.8495
35.19830.3202-0.451.042-0.30170.3221-0.61090.7654-0.481-0.02020.47470.33120.6160.2648-0.10720.9852-0.0111-0.05140.9216-0.00710.743966.4106-26.581612.7293
40.2038-0.1254-0.32280.24340.2050.1333-0.0701-0.0995-0.20260.48660.1724-0.33010.04040.18650.00010.62880.1288-0.06280.7766-0.03460.666175.3243-18.715219.8606
50.05080.02680.10640.0473-0.03870.11380.4007-0.52770.73230.4161-0.4571-0.0680.96730.0484-0.00111.24440.2031-0.16491.19590.0571.401381.6098-15.657528.4928
60.11430.42130.40480.09210.21850.15810.46470.02730.1661.2851-0.1925-0.22650.80180.0985-0.00011.41280.00910.0260.88920.00450.76669.1449-23.097131.7851
70.2127-0.030.17850.0513-0.05280.1437-0.33210.02670.9059-0.1021-0.5826-0.31330.88690.2461-0.00191.06170.05170.3581.18110.15031.562487.991815.2352-6.448
80.59030.1926-0.80370.4965-0.00120.9738-0.53550.2613-0.4621-1.2001-0.2343-0.36760.4651-0.1089-0.00520.94270.080.230.7208-0.04561.009675.988713.4136-0.4768
90.6462-0.05090.52581.8635-1.00961.22190.0067-0.2239-0.24290.1271-0.1441-0.43470.1839-0.02050.00550.6299-0.0238-0.03480.6931-0.00370.718970.043614.789715.0051
101.9661.8448-1.09646.5558-0.96931.40440.42480.20250.4187-0.49580.05121.1105-0.1229-0.79440.5150.7140.0740.08860.703-0.00760.653967.788527.35788.3184
115.78020.2991-0.31993.67253.57438.34711.17370.381.97390.01021.7437-0.7361-4.13051.14850.89260.2970.4498-0.49230.50860.2175-0.142456.893730.228612.3443
120.1389-0.1634-0.06730.118-0.0644-0.00840.34270.07350.6603-0.0266-0.08520.16920.7658-0.10370.00021.05540.0650.07930.9967-0.04380.902458.584420.928219.7292
132.54351.66781.47984.2684-1.59123.48240.5521-0.57940.6880.6817-0.11830.8471-0.4844-1.3695-1.7090.7053-0.00370.1241.09020.11061.132347.760120.687619.7342
140.65350.4663-0.22280.8425-0.27350.40570.888-1.21830.78941.6988-0.32720.597-1.5314-0.21280.01331.8434-0.12210.1041.3196-0.05490.739760.243825.322729.1056
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection detailsAuth asym-IDAuth seq-ID
1X-RAY DIFFRACTION1chain 'A' and (resid 78 through 188 )A78 - 188
2X-RAY DIFFRACTION2chain 'A' and (resid 189 through 249 )A189 - 249
3X-RAY DIFFRACTION3chain 'A' and (resid 250 through 284 )A250 - 284
4X-RAY DIFFRACTION4chain 'A' and (resid 285 through 316 )A285 - 316
5X-RAY DIFFRACTION5chain 'A' and (resid 317 through 329 )A317 - 329
6X-RAY DIFFRACTION6chain 'A' and (resid 330 through 361 )A330 - 361
7X-RAY DIFFRACTION7chain 'B' and (resid 77 through 104 )B77 - 104
8X-RAY DIFFRACTION8chain 'B' and (resid 105 through 164 )B105 - 164
9X-RAY DIFFRACTION9chain 'B' and (resid 165 through 249 )B165 - 249
10X-RAY DIFFRACTION10chain 'B' and (resid 250 through 270 )B250 - 270
11X-RAY DIFFRACTION11chain 'B' and (resid 271 through 284 )B271 - 284
12X-RAY DIFFRACTION12chain 'B' and (resid 285 through 301 )B285 - 301
13X-RAY DIFFRACTION13chain 'B' and (resid 302 through 329 )B302 - 329
14X-RAY DIFFRACTION14chain 'B' and (resid 330 through 361 )B330 - 361

+
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