[English] 日本語
Yorodumi
- PDB-8fba: Crystal structure of Ky315 Fab in complex with circumsporozoite p... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8fba
TitleCrystal structure of Ky315 Fab in complex with circumsporozoite protein DND peptide
Components
  • Circumsporozoite protein DND peptide
  • Ky315 Antibody, heavy chain
  • Ky315 Antibody, light chain
KeywordsIMMUNE SYSTEM / Malaria / Antibody
Function / homology
Function and homology information


side of membrane / cell surface / plasma membrane / cytoplasm
Similarity search - Function
Plasmodium circumsporozoite protein / Thrombospondin type 1 domain / Thrombospondin type-1 (TSP1) repeat superfamily / Thrombospondin type-1 (TSP1) repeat profile. / Thrombospondin type 1 repeats / Thrombospondin type-1 (TSP1) repeat
Similarity search - Domain/homology
Circumsporozoite protein
Similarity search - Component
Biological speciesMus musculus (house mouse)
Plasmodium falciparum (malaria parasite P. falciparum)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.96 Å
AuthorsBurn Aschner, C. / Julien, J.P.
Funding support United States, 1items
OrganizationGrant numberCountry
Bill & Melinda Gates FoundationOPP1179906 United States
CitationJournal: Cell Rep / Year: 2023
Title: Molecular determinants of cross-reactivity and potency by VH3-33 antibodies against the Plasmodium falciparum circumsporozoite protein.
Authors: Thai, E. / Murugan, R. / Binter, S. / Burn Aschner, C. / Prieto, K. / Kassardjian, A. / Obraztsova, A.S. / Kang, R.W. / Flores-Garcia, Y. / Mathis-Torres, S. / Li, K. / Horn, G.Q. / ...Authors: Thai, E. / Murugan, R. / Binter, S. / Burn Aschner, C. / Prieto, K. / Kassardjian, A. / Obraztsova, A.S. / Kang, R.W. / Flores-Garcia, Y. / Mathis-Torres, S. / Li, K. / Horn, G.Q. / Huntwork, R.H.C. / Bolscher, J.M. / de Bruijni, M.H.C. / Sauerwein, R. / Dennison, S.M. / Tomaras, G.D. / Zavala, F. / Kellam, P. / Wardemann, H. / Julien, J.P.
History
DepositionNov 29, 2022Deposition site: RCSB / Processing site: RCSB
Revision 1.0Nov 1, 2023Provider: repository / Type: Initial release
Revision 1.1Dec 13, 2023Group: Database references / Category: citation / citation_author
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_PubMed / _citation.title
Revision 1.2Mar 20, 2024Group: Source and taxonomy / Category: pdbx_entity_src_syn
Item: _pdbx_entity_src_syn.ncbi_taxonomy_id / _pdbx_entity_src_syn.organism_scientific

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Ky315 Antibody, heavy chain
B: Ky315 Antibody, light chain
C: Ky315 Antibody, heavy chain
D: Ky315 Antibody, light chain
P: Circumsporozoite protein DND peptide
Q: Circumsporozoite protein DND peptide
hetero molecules


Theoretical massNumber of molelcules
Total (without water)98,09516
Polymers97,4756
Non-polymers62110
Water11,998666
1
A: Ky315 Antibody, heavy chain
B: Ky315 Antibody, light chain
P: Circumsporozoite protein DND peptide
hetero molecules


Theoretical massNumber of molelcules
Total (without water)49,17210
Polymers48,7373
Non-polymers4347
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area5870 Å2
ΔGint-18 kcal/mol
Surface area20330 Å2
MethodPISA
2
C: Ky315 Antibody, heavy chain
D: Ky315 Antibody, light chain
Q: Circumsporozoite protein DND peptide
hetero molecules


Theoretical massNumber of molelcules
Total (without water)48,9246
Polymers48,7373
Non-polymers1863
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area5120 Å2
ΔGint-24 kcal/mol
Surface area19850 Å2
MethodPISA
Unit cell
Length a, b, c (Å)67.348, 65.245, 128.690
Angle α, β, γ (deg.)90.000, 97.250, 90.000
Int Tables number4
Space group name H-MP1211
Space group name HallP2yb

-
Components

#1: Antibody Ky315 Antibody, heavy chain


Mass: 24060.014 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Production host: Homo sapiens (human)
#2: Antibody Ky315 Antibody, light chain


Mass: 23412.059 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Production host: Homo sapiens (human)
#3: Protein/peptide Circumsporozoite protein DND peptide / CS


Mass: 1265.286 Da / Num. of mol.: 2 / Source method: obtained synthetically
Source: (synth.) Plasmodium falciparum (isolate NF54) (eukaryote)
References: UniProt: P08307
#4: Chemical
ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 10 / Source method: isolated from a natural source / Formula: C2H6O2
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 666 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestN

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.91 Å3/Da / Density % sol: 57.71 %
Crystal growTemperature: 293.15 K / Method: vapor diffusion, sitting drop / Details: 0.2 M magnesium formate pH 5.9, 20% PEG3350

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: NSLS-II / Beamline: 17-ID-1 / Wavelength: 0.920088 Å
DetectorType: DECTRIS EIGER X 9M / Detector: PIXEL / Date: Sep 1, 2020
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.920088 Å / Relative weight: 1
ReflectionResolution: 1.96→40 Å / Num. obs: 79772 / % possible obs: 100 % / Redundancy: 7 % / Biso Wilson estimate: 27.19 Å2 / CC1/2: 0.996 / Net I/σ(I): 9.6
Reflection shellResolution: 1.96→1.99 Å / Num. unique obs: 3529 / CC1/2: 0.531

-
Processing

Software
NameVersionClassification
PHENIX1.20.1_4487refinement
XDSdata reduction
XSCALEdata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB ID 6ULF
Resolution: 1.96→39.37 Å / SU ML: 0.2354 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 21.8866
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.22 1999 2.51 %
Rwork0.1777 77750 -
obs0.1788 79749 99.97 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 35.8 Å2
Refinement stepCycle: LAST / Resolution: 1.96→39.37 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms6730 0 40 666 7436
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00537119
X-RAY DIFFRACTIONf_angle_d0.75839711
X-RAY DIFFRACTIONf_chiral_restr0.05121079
X-RAY DIFFRACTIONf_plane_restr0.00541267
X-RAY DIFFRACTIONf_dihedral_angle_d12.84842541
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.96-2.010.33931410.27515504X-RAY DIFFRACTION99.98
2.01-2.060.29761420.24675528X-RAY DIFFRACTION99.96
2.06-2.120.29251420.23785529X-RAY DIFFRACTION99.98
2.12-2.190.25831420.22255501X-RAY DIFFRACTION99.93
2.19-2.270.24331420.2075527X-RAY DIFFRACTION99.98
2.27-2.360.23971420.19565522X-RAY DIFFRACTION100
2.36-2.470.24571420.1915551X-RAY DIFFRACTION99.98
2.47-2.60.22961430.19435550X-RAY DIFFRACTION99.91
2.6-2.760.21031420.18835530X-RAY DIFFRACTION99.98
2.76-2.980.24381430.18475538X-RAY DIFFRACTION100
2.98-3.270.22841430.17935573X-RAY DIFFRACTION100
3.27-3.750.22151440.1645582X-RAY DIFFRACTION100
3.75-4.720.17871440.13615595X-RAY DIFFRACTION99.95
4.72-39.370.16931470.15125720X-RAY DIFFRACTION99.91
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)
12.73986026416-1.23869816339-0.2767396628472.067166117880.8697180704921.25248218280.1383304992320.2696898272220.202418029588-0.644593765003-0.2027640516820.129164444893-0.209184574155-0.1936781683230.04384062095260.3808625699010.0887400181555-0.05825201078370.2585063693250.01434038254870.21197178394213.15694664531.6280330312435.0436408768
22.42511973625-0.1985595807641.108898020443.363215223771.137248073992.946674376910.0422102138478-0.08471318640040.1245350913680.137912974479-0.1183878836850.0153150552079-0.065980361569-0.1020056291980.08066313015190.11490009816-0.00220966600595-0.008099435588840.2060741475250.008088214637120.214346875428-0.98479881372924.110773963361.4089094393
31.535231834590.006233780873040.4654115391922.516651734981.352510696172.3260365854-0.00177657422989-0.09935154262720.0402819811891-0.123017234565-0.00477888858002-0.13180638727-0.0884312182147-0.01206628598220.0004236911220210.1318299579250.0158022680734-0.01539617285220.1651013128370.008170567744760.16975008362825.7257050566-1.5955034717353.5927276072
43.372074091170.21892057546-0.1017007071211.14842772787-0.1432758838761.294485419940.05552892294290.0338238278909-0.04536359759310.0507105274854-0.01667884866430.176585075168-0.00949232396992-0.169709026939-0.03426310102410.133292736234-0.00182894089334-0.008304755787320.200895269604-0.01374889025460.185742394376-1.7030728138511.923795794471.344694864
52.09266853944-0.205666489504-0.2802851982722.251565856830.5035274154452.546411218690.01540497744180.13844333386-0.085507702767-0.261559448680.02890424711460.2040694383650.14726669277-0.115216723377-0.0218598849730.22751170340.00689224203119-0.06466435771560.202496925621-0.004993107067480.18154103244514.276686244829.276804670130.0493167724
61.830365980580.03600625510990.9757820176362.924714079091.118230936962.54441244832-0.210716305743-0.0666367437191-0.368051109430.4579722896650.0632480075177-0.02702492908390.8535311251850.01686151087110.09866149467170.9655306215090.04480626831160.1079577879780.342545272194-0.01169482952860.30683709560132.61380827717.071771765247.87498735857
72.84982819057-1.081704478260.3383579793212.81682263187-0.0004602267305622.476261519620.0644163627780.0880580349032-0.205770026415-0.06561305578720.0281267163892-0.129425196840.2634438928150.273221022887-0.09536200106530.2246377015330.0396532511959-0.03092138425090.237840617975-0.03713394701410.1789000342335.800412226930.516593673936.2215554643
81.93601660426-0.225221131019-0.4009162005231.326432281880.3313448017075.131094528580.008272973933730.1164455113990.0895042566773-0.4277278208310.244871191203-0.2829931064190.09022973737080.365647449433-0.2609545147210.7087977695430.0716924786890.1379870258820.371761782242-0.07427902156810.35223137690743.40437243819.23043589243.85906586398
95.798189018491.374705654173.117456776752.0818351058-1.006913260663.415334979490.1477369544620.366846618244-0.19253595623-0.5142249225230.205447462401-0.442245100995-0.52577668922-0.00579610622282-0.1822762411730.4806689808910.07928223497290.09702567672060.279741901056-0.003512596090030.18319329921424.144441684-10.281634870730.1650651466
105.49325407113-0.1065821821614.336481278659.44174007451-4.024382358235.27517422885-0.111759264856-0.4387007378390.05875493635540.8185129605190.08536960311630.415561818673-0.197303649902-0.0129461166757-0.04466564343260.2281389947020.03614808304860.03137406512140.244085571402-0.05208877316180.16965005566514.277857196540.584373028142.7325477045
Refinement TLS group

Refine-ID: X-RAY DIFFRACTION

IDRefine TLS-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11chain 'A' and (resid 1 through 113 )AA1 - 1131 - 124
22chain 'A' and (resid 114 through 216 )AA114 - 216125 - 227
33chain 'B' and (resid 1 through 107)BB1 - 1071 - 106
44chain 'B' and (resid 108 through 214 )BB108 - 214107 - 213
55chain 'C' and (resid 1 through 113 )CC1 - 1131 - 124
66chain 'C' and (resid 114 through 214 )CC114 - 214125 - 219
77chain 'D' and (resid 1 through 107 )DD1 - 1071 - 106
88chain 'D' and (resid 108 through 213 )DD108 - 213107 - 212
99chain 'P' and (resid 1 through 11 )PE1 - 111 - 11
1010chain 'Q' and (resid 1 through 11 )QF1 - 111 - 11

+
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