[English] 日本語
Yorodumi
- PDB-7o2m: Crystal Structure of Unlinked NS2B-NS3 Protease from Zika Virus i... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 7o2m
TitleCrystal Structure of Unlinked NS2B-NS3 Protease from Zika Virus in Complex with Inhibitor MI-2289
Components(Genome polyprotein) x 2
KeywordsVIRAL PROTEIN / FLAVIVIRIN / SERINE PROTEASE / NS2B-NS3 / ZIKA VIRUS
Function / homology
Function and homology information


symbiont-mediated suppression of host JAK-STAT cascade via inhibition of STAT2 activity / ribonucleoside triphosphate phosphatase activity / double-stranded RNA binding / viral capsid / mRNA (nucleoside-2'-O-)-methyltransferase activity / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / RNA helicase activity / host cell endoplasmic reticulum membrane / protein dimerization activity / symbiont-mediated suppression of host type I interferon-mediated signaling pathway ...symbiont-mediated suppression of host JAK-STAT cascade via inhibition of STAT2 activity / ribonucleoside triphosphate phosphatase activity / double-stranded RNA binding / viral capsid / mRNA (nucleoside-2'-O-)-methyltransferase activity / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / RNA helicase activity / host cell endoplasmic reticulum membrane / protein dimerization activity / symbiont-mediated suppression of host type I interferon-mediated signaling pathway / symbiont entry into host cell / viral RNA genome replication / serine-type endopeptidase activity / RNA-dependent RNA polymerase activity / fusion of virus membrane with host endosome membrane / virion attachment to host cell / virion membrane / structural molecule activity / proteolysis / extracellular region / ATP binding / membrane / metal ion binding
Similarity search - Function
: / Flavivirus capsid protein C superfamily / RNA-directed RNA polymerase, thumb domain, Flavivirus / Flavivirus RNA-directed RNA polymerase, thumb domain / Flavivirus envelope glycoprotein E, stem/anchor domain / Flavivirus non-structural protein NS2B / : / Flavivirus NS3 helicase, C-terminal helical domain / Genome polyprotein, Flavivirus / Flavivirus non-structural protein NS4A ...: / Flavivirus capsid protein C superfamily / RNA-directed RNA polymerase, thumb domain, Flavivirus / Flavivirus RNA-directed RNA polymerase, thumb domain / Flavivirus envelope glycoprotein E, stem/anchor domain / Flavivirus non-structural protein NS2B / : / Flavivirus NS3 helicase, C-terminal helical domain / Genome polyprotein, Flavivirus / Flavivirus non-structural protein NS4A / Flavivirus non-structural protein NS2B / Flavivirus capsid protein C / Flavivirus non-structural protein NS4B / mRNA cap 0/1 methyltransferase / Flavivirus capsid protein C / Flavivirus non-structural protein NS4B / Flavivirus non-structural protein NS4A / Flavivirus NS2B domain profile. / mRNA cap 0 and cap 1 methyltransferase (EC 2.1.1.56 and EC 2.1.1.57) domain profile. / Flavivirus non-structural protein NS2A / Flavivirus non-structural protein NS2A / Flavivirus NS3, petidase S7 / Peptidase S7, Flavivirus NS3 serine protease / Flavivirus NS3 protease (NS3pro) domain profile. / RNA-directed RNA polymerase, flavivirus / Flavivirus RNA-directed RNA polymerase, fingers and palm domains / Flavivirus non-structural Protein NS1 / Flavivirus non-structural protein NS1 / Envelope glycoprotein M, flavivirus / Flavivirus envelope glycoprotein M / Envelope glycoprotein M superfamily, flavivirus / Flavivirus polyprotein propeptide / Flavivirus polyprotein propeptide superfamily / Flavivirus polyprotein propeptide / Flaviviral glycoprotein E, central domain, subdomain 1 / Flaviviral glycoprotein E, central domain, subdomain 2 / Flavivirus envelope glycoprotein E, Stem/Anchor domain / Flavivirus glycoprotein E, immunoglobulin-like domain / Flavivirus envelope glycoprotein E, Stem/Anchor domain superfamily / Flavivirus glycoprotein, immunoglobulin-like domain / Flavivirus glycoprotein central and dimerisation domain / Flavivirus glycoprotein, central and dimerisation domains / Ribosomal RNA methyltransferase, FtsJ domain / FtsJ-like methyltransferase / Flavivirus/Alphavirus glycoprotein, immunoglobulin-like domain superfamily / Flavivirus glycoprotein, central and dimerisation domain superfamily / Flaviviral glycoprotein E, dimerisation domain / DEAD box, Flavivirus / Flavivirus DEAD domain / helicase superfamily c-terminal domain / Immunoglobulin E-set / Superfamilies 1 and 2 helicase C-terminal domain profile. / Superfamilies 1 and 2 helicase ATP-binding type-1 domain profile. / DEAD-like helicases superfamily / Helicase, C-terminal / Helicase superfamily 1/2, ATP-binding domain / RNA-directed RNA polymerase, catalytic domain / RdRp of positive ssRNA viruses catalytic domain profile. / S-adenosyl-L-methionine-dependent methyltransferase superfamily / Peptidase S1, PA clan / DNA/RNA polymerase superfamily / P-loop containing nucleoside triphosphate hydrolase
Similarity search - Domain/homology
Chem-UZZ / Genome polyprotein
Similarity search - Component
Biological speciesZika virus
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.9 Å
AuthorsHuber, S. / Heine, A. / Steinmetzer, T.
CitationJournal: J.Med.Chem. / Year: 2022
Title: Structure-Based Optimization and Characterization of Macrocyclic Zika Virus NS2B-NS3 Protease Inhibitors.
Authors: Huber, S. / Braun, N.J. / Schmacke, L.C. / Quek, J.P. / Murra, R. / Bender, D. / Hildt, E. / Luo, D. / Heine, A. / Steinmetzer, T.
History
DepositionMar 30, 2021Deposition site: PDBE / Processing site: PDBE
Revision 1.0Apr 6, 2022Provider: repository / Type: Initial release
Revision 1.1Dec 21, 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.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year
Revision 1.2Jan 31, 2024Group: 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: Genome polyprotein
B: Genome polyprotein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)25,6053
Polymers24,9032
Non-polymers7021
Water1,964109
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area4010 Å2
ΔGint-26 kcal/mol
Surface area9140 Å2
MethodPISA
Unit cell
Length a, b, c (Å)42.274, 42.274, 216.109
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number95
Space group name H-MP4322
Space group name HallP4cw2c
Symmetry operation#1: x,y,z
#2: -y,x,z+3/4
#3: y,-x,z+1/4
#4: x,-y,-z+1/2
#5: -x,y,-z
#6: -x,-y,z+1/2
#7: y,x,-z+1/4
#8: -y,-x,-z+3/4
Components on special symmetry positions
IDModelComponents
11B-351-

HOH

21B-373-

HOH

31B-380-

HOH

-
Components

#1: Protein Genome polyprotein


Mass: 5865.384 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Zika virus / Plasmid: bZiPro / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: H8XX12
#2: Protein Genome polyprotein


Mass: 19037.592 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Zika virus / Plasmid: bZiPro / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: H8XX12
#3: Chemical ChemComp-UZZ / 1-[(3~{S},6~{S},9~{S},19~{R})-3,6-bis(4-azanylbutyl)-2,5,8,12,15,18-hexakis(oxidanylidene)-9-(phenylmethyl)-1,4,7,11,14,17-hexazacyclotricos-19-yl]guanidine


Mass: 701.860 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C33H55N11O6 / Feature type: SUBJECT OF INVESTIGATION
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 109 / 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: 1.97 Å3/Da / Density % sol: 37.53 %
Crystal growTemperature: 291 K / Method: vapor diffusion, hanging drop / pH: 4.6
Details: 0.1 M sodium acetate 0.2 M ammonium sulfate 18 % PEG2000

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: BESSY / Beamline: 14.2 / Wavelength: 0.9184 Å
DetectorType: DECTRIS PILATUS3 S 2M / Detector: PIXEL / Date: Oct 17, 2020
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9184 Å / Relative weight: 1
ReflectionResolution: 1.9→43.22 Å / Num. obs: 15560 / % possible obs: 94.1 % / Redundancy: 7.92 % / Biso Wilson estimate: 28.3 Å2 / CC1/2: 0.999 / Rsym value: 0.075 / Net I/σ(I): 14.32
Reflection shellResolution: 1.9→2.01 Å / Mean I/σ(I) obs: 2.17 / Num. unique obs: 2250 / CC1/2: 0.93 / Rsym value: 0.44

-
Processing

Software
NameVersionClassification
XDSdata scaling
XDSdata reduction
PHASERphasing
Cootmodel building
PHENIX1.16_3549refinement
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 5GPI
Resolution: 1.9→39.37 Å / SU ML: 0.2277 / Cross valid method: FREE R-VALUE / σ(F): 1.38 / Phase error: 26.0539
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.2506 777 5 %
Rwork0.1831 14758 -
obs0.1865 15535 93.94 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 42.51 Å2
Refinement stepCycle: LAST / Resolution: 1.9→39.37 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1408 0 50 109 1567
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00971494
X-RAY DIFFRACTIONf_angle_d0.99812032
X-RAY DIFFRACTIONf_chiral_restr0.0608225
X-RAY DIFFRACTIONf_plane_restr0.0066272
X-RAY DIFFRACTIONf_dihedral_angle_d14.2395881
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.9-2.020.31241160.2642203X-RAY DIFFRACTION86.4
2.02-2.170.29381180.23362246X-RAY DIFFRACTION89.27
2.17-2.390.27631250.20982367X-RAY DIFFRACTION91.65
2.39-2.740.27561330.22312512X-RAY DIFFRACTION97.42
2.74-3.450.26921370.18272612X-RAY DIFFRACTION98.88
3.45-39.370.21381480.14922818X-RAY DIFFRACTION99.16
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)
14.882840145114.8430956657-4.884025374574.79942810456-4.840789155964.8818212835-0.0456587327292-0.186178587398-0.263553177597-0.07668889096-0.267207086643-0.4990767240260.1743388685190.4272511971020.3542438250140.4330402525970.1381330286730.005965325235390.312359865595-0.02942933375280.30947464644326.145274296-10.5593918646-18.1010570804
24.384966360020.660045854935-0.8464113697111.52165223588-1.474370693584.289553063680.1366332387360.2085085208270.11848274645-0.379187131677-0.1114871775190.1990345844860.21284602659-0.170395858095-0.02708475250830.3324126352020.136944143718-0.01677450739660.230102647558-0.02360169782330.269792061388.846382039325.86982513952-19.3633152047
37.823154199896.12800836878-2.855184042598.15105806468-3.750231000584.40090828550.750904133282-0.468189390117-0.3794716732310.438392176481-0.620446838588-0.2484875340290.08097667441250.908450505381-0.123283365480.2932591650190.0964327835562-0.007888614977880.394047438609-0.04790965227550.21898091697627.0533629664-8.83504332026-17.684015305
47.011919868253.260592370980.4238373926121.902028358971.115472921853.972319242330.166051761706-0.0183125322057-0.7460378115330.0461661301625-0.230724357271-0.3214031810720.595518242091-0.03166437220.08901710393460.3148842467630.0765840107179-0.004314682652420.249863004087-0.009697406390840.29217404432520.2276718161-12.6848945628-15.5923786968
53.595678572225.731375404460.07800458287729.682934345991.252289097086.946365360120.3380551283640.108741562637-0.2441270707010.0223301201791-0.410989659388-0.1900291211750.1356540695830.314779117401-0.04410313461880.234611551550.0793560903086-0.02144992383670.240795901307-0.01286947632980.19445705657822.0432109645-3.47567362322-10.1772046906
62.438387338540.511150825412-0.2555713584072.44409568442.891982210183.741283894090.296760594003-0.400152544047-0.4862185458360.2447479076980.21128379261-0.269838624540.8595713767060.270269745792-0.4154781328170.480569006390.0678978719152-0.131300533470.279926534240.02562682810070.31587533240126.2409222473-8.41378347996-5.70328223464
78.58252101328-1.81211300451-5.064966771161.94710802143-1.077675656349.514766018810.223860498048-0.3396493507560.130298254239-0.0222983230887-0.0671104535841-0.0440388960135-0.3514907868790.00940079864342-0.136775120660.2918643472690.0372985000196-0.05734492825550.266890803335-0.02880590616310.21507354001618.2435451103-0.33502363017-6.02264751727
87.34787902992-2.754180149814.705660580194.79188825995-4.126778317258.625947265870.1357671599080.4743086854520.4786546910560.0763578369141-0.367265489641-0.0634342510897-0.7373260886620.5034508003770.1874387180370.2822051981040.07036205893050.07361026296240.237516239330.0003453887013530.22162375228722.02054406649.24838797716-16.276547749
95.084803667383.519429650550.0356462255513.50741928094-1.435131059322.069617874560.2643135775590.505554578489-0.223696444864-0.344368423819-0.339478477142-0.345571794712-0.0815248669919-0.195317307692-0.002230074808050.3103554727250.180590455046-0.01507729968540.385635892675-0.02104448597360.20201396891418.1276796714-4.98494616213-26.4933171841
107.83292065197-3.7284561822-3.376040656626.710620561750.02513993494623.877211952170.3602688878930.5121076635450.170906251719-0.654502705213-0.2373510283410.128005149645-0.343036322799-0.133526680574-0.1694801387890.276178026580.115445211319-0.0790015304940.2836927517330.002539806423160.21999013772711.58888361527.29195786506-23.4535064126
113.21806423553-1.04962776320.01892324165365.66333351611-1.684439583320.8538948563760.1295567329320.07330319521830.221229625669-0.100687712772-0.1847409927080.127906252423-0.277459587661-0.3561806817440.1103079190270.2743160294180.126620843431-0.04217010709910.394514639065-0.02325323192480.22346577353310.56819204792.46079754423-17.7731182028
122.47520663324-2.406737767041.331644048639.1008901091-7.953185925767.807028468910.1243314683150.5566767206280.575705242121-0.534661598764-0.3015330349040.0601080349303-0.2801011161850.3204241019380.1737866177950.3427328650950.1037414877160.03546572349370.2730745447740.03622337146980.30268633707823.36117245867.67206141107-23.1052457318
137.233458657443.81480470456-2.778920491086.056364631430.3329118158442.080338450370.01636308474970.2494845541380.155222966854-0.177090082203-0.04344359315970.2647823243540.0680527462703-0.2451618866140.08598021832640.3162054214990.110829674404-0.06001379924390.2467738433080.008851293175560.20272013242911.02368444863.34782899757-16.5960914164
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resid 50 through 59 )
2X-RAY DIFFRACTION2chain 'A' and (resid 60 through 87 )
3X-RAY DIFFRACTION3chain 'B' and (resid 17 through 27 )
4X-RAY DIFFRACTION4chain 'B' and (resid 28 through 42 )
5X-RAY DIFFRACTION5chain 'B' and (resid 43 through 53 )
6X-RAY DIFFRACTION6chain 'B' and (resid 54 through 71 )
7X-RAY DIFFRACTION7chain 'B' and (resid 72 through 79 )
8X-RAY DIFFRACTION8chain 'B' and (resid 80 through 94 )
9X-RAY DIFFRACTION9chain 'B' and (resid 95 through 106 )
10X-RAY DIFFRACTION10chain 'B' and (resid 107 through 118 )
11X-RAY DIFFRACTION11chain 'B' and (resid 119 through 137 )
12X-RAY DIFFRACTION12chain 'B' and (resid 138 through 145 )
13X-RAY DIFFRACTION13chain 'B' and (resid 146 through 170 )

+
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