[English] 日本語
Yorodumi
- PDB-7kdm: Ricin bound to VHH antibody V5G6 -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 7kdm
TitleRicin bound to VHH antibody V5G6
Components
  • Anti-RON nanobody
  • Ricin chain A
  • Ricin chain B
KeywordsTOXIN / Ribosome inactivating protein / VHH antibody
Function / homology
Function and homology information


rRNA N-glycosylase / rRNA N-glycosylase activity / AMP binding / defense response / toxin activity / carbohydrate binding / killing of cells of another organism / negative regulation of translation
Similarity search - Function
Ribosome-inactivating protein conserved site / Shiga/ricin ribosomal inactivating toxins active site signature. / Ricin-type beta-trefoil lectin domain / Ribosome-inactivating protein type 1/2 / Ribosome-inactivating protein / Ribosome-inactivating protein, subdomain 1 / Ribosome-inactivating protein, subdomain 2 / Ribosome-inactivating protein superfamily / Ribosome inactivating protein / Ricin-type beta-trefoil ...Ribosome-inactivating protein conserved site / Shiga/ricin ribosomal inactivating toxins active site signature. / Ricin-type beta-trefoil lectin domain / Ribosome-inactivating protein type 1/2 / Ribosome-inactivating protein / Ribosome-inactivating protein, subdomain 1 / Ribosome-inactivating protein, subdomain 2 / Ribosome-inactivating protein superfamily / Ribosome inactivating protein / Ricin-type beta-trefoil / Lectin domain of ricin B chain profile. / Ricin B, lectin domain / Ricin B-like lectins
Similarity search - Domain/homology
Biological speciesLama glama (llama)
Ricinus communis (castor bean)
MethodX-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 2.301 Å
AuthorsRudolph, M.J.
Funding support United States, 1items
OrganizationGrant numberCountry
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)HHSN272201400021C United States
CitationJournal: J.Mol.Biol. / Year: 2021
Title: Structural Analysis of Toxin-Neutralizing, Single-Domain Antibodies that Bridge Ricin's A-B Subunit Interface.
Authors: Rudolph, M.J. / Poon, A.Y. / Kavaliauskiene, S. / Myrann, A.G. / Reynolds-Peterson, C. / Davis, S.A. / Sandvig, K. / Vance, D.J. / Mantis, N.J.
History
DepositionOct 8, 2020Deposition site: RCSB / Processing site: RCSB
Revision 1.0Aug 4, 2021Provider: repository / Type: Initial release
Revision 1.1Oct 18, 2023Group: 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 / struct_ncs_dom_lim
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_ncs_dom_lim.beg_auth_comp_id / _struct_ncs_dom_lim.beg_label_asym_id / _struct_ncs_dom_lim.beg_label_comp_id / _struct_ncs_dom_lim.beg_label_seq_id / _struct_ncs_dom_lim.end_auth_comp_id / _struct_ncs_dom_lim.end_label_asym_id / _struct_ncs_dom_lim.end_label_comp_id / _struct_ncs_dom_lim.end_label_seq_id
Revision 1.2Nov 20, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Ricin chain A
B: Ricin chain B
C: Anti-RON nanobody
D: Ricin chain A
E: Ricin chain B
F: Anti-RON nanobody
hetero molecules


Theoretical massNumber of molelcules
Total (without water)149,06924
Polymers145,6176
Non-polymers3,45218
Water10,917606
1
A: Ricin chain A
B: Ricin chain B
C: Anti-RON nanobody
hetero molecules


Theoretical massNumber of molelcules
Total (without water)74,48411
Polymers72,8093
Non-polymers1,6758
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area7550 Å2
ΔGint-119 kcal/mol
Surface area24890 Å2
MethodPISA
2
D: Ricin chain A
E: Ricin chain B
F: Anti-RON nanobody
hetero molecules


Theoretical massNumber of molelcules
Total (without water)74,58513
Polymers72,8093
Non-polymers1,77610
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area7790 Å2
ΔGint-99 kcal/mol
Surface area25090 Å2
MethodPISA
Unit cell
Length a, b, c (Å)44.345, 77.438, 101.577
Angle α, β, γ (deg.)89.970, 90.180, 89.980
Int Tables number1
Space group name H-MP1
Noncrystallographic symmetry (NCS)NCS domain:
IDEns-IDDetails
11(chain A and (resid 5 through 205 or resid 207 through 261))
21(chain D and (resid 5 through 205 or resid 207 through 261))
12(chain B and (resid 3 through 19 or resid 21 through 262))
22(chain E and (resid 3 through 19 or resid 21 through 262))
13(chain C and (resid 3 through 20 or resid 22 through 25 or resid 30 through 120))
23(chain F and (resid 3 through 9 or resid 11 through 20 or resid 22 through 120))

NCS domain segments:
Dom-IDComponent-IDEns-IDBeg auth comp-IDBeg label comp-IDEnd auth comp-IDEnd label comp-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
111GLNGLNILEILE(chain A and (resid 5 through 205 or resid 207 through 261))AA5 - 2055 - 205
121LEULEUPROPRO(chain A and (resid 5 through 205 or resid 207 through 261))AA207 - 261207 - 261
211GLNGLNILEILE(chain D and (resid 5 through 205 or resid 207 through 261))DD5 - 2055 - 205
221LEULEUPROPRO(chain D and (resid 5 through 205 or resid 207 through 261))DD207 - 261207 - 261
112VALVALLEULEU(chain B and (resid 3 through 19 or resid 21 through 262))BB3 - 193 - 19
122VALVALPHEPHE(chain B and (resid 3 through 19 or resid 21 through 262))BB21 - 26221 - 262
212VALVALLEULEU(chain E and (resid 3 through 19 or resid 21 through 262))EE3 - 193 - 19
222VALVALPHEPHE(chain E and (resid 3 through 19 or resid 21 through 262))EE21 - 26221 - 262
113GLNGLNLEULEU(chain C and (resid 3 through 20 or resid 22 through 25 or resid 30 through 120))CC3 - 203 - 20
123CYSCYSSERSER(chain C and (resid 3 through 20 or resid 22 through 25 or resid 30 through 120))CC22 - 2522 - 25
133SERSERVALVAL(chain C and (resid 3 through 20 or resid 22 through 25 or resid 30 through 120))CC30 - 12030 - 120
213GLNGLNGLYGLY(chain F and (resid 3 through 9 or resid 11 through 20 or resid 22 through 120))FF3 - 93 - 9
223LEULEULEULEU(chain F and (resid 3 through 9 or resid 11 through 20 or resid 22 through 120))FF11 - 2011 - 20
233CYSCYSVALVAL(chain F and (resid 3 through 9 or resid 11 through 20 or resid 22 through 120))FF22 - 12022 - 120

NCS ensembles :
ID
1
2
3

-
Components

-
Protein , 2 types, 4 molecules ADBE

#1: Protein Ricin chain A


Mass: 29936.758 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Details: Glycosidase / Source: (natural) Ricinus communis (castor bean)
#2: Protein Ricin chain B


Mass: 28989.580 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Details: Lectin / Source: (natural) Ricinus communis (castor bean) / References: UniProt: P02879, rRNA N-glycosylase

-
Antibody , 1 types, 2 molecules CF

#3: Antibody Anti-RON nanobody


Mass: 13882.364 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Details: VHH antibody / Source: (gene. exp.) Lama glama (llama) / Production host: Escherichia coli (E. coli)

-
Sugars , 3 types, 6 molecules

#4: Polysaccharide alpha-L-fucopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-glucopyranose


Type: oligosaccharide / Mass: 367.349 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
DescriptorTypeProgram
LFucpa1-3DGlcpNAcb1-ROHGlycam Condensed SequenceGMML 1.0
WURCS=2.0/2,2,1/[a2122h-1b_1-5_2*NCC/3=O][a1221m-1a_1-5]/1-2/a3-b1WURCSPDB2Glycan 1.1.0
[][D-1-deoxy-GlcpNAc]{[(3+1)][a-L-Fucp]{}}LINUCSPDB-CARE
#5: Polysaccharide 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose


Type: oligosaccharide / Mass: 424.401 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
DescriptorTypeProgram
DGlcpNAcb1-4DGlcpNAcb1-ROHGlycam Condensed SequenceGMML 1.0
WURCS=2.0/1,2,1/[a2122h-1b_1-5_2*NCC/3=O]/1-1/a4-b1WURCSPDB2Glycan 1.1.0
[][D-1-deoxy-GlcpNAc]{[(4+1)][b-D-GlcpNAc]{}}LINUCSPDB-CARE
#6: Polysaccharide beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta- ...beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose


Type: oligosaccharide / Mass: 586.542 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
DescriptorTypeProgram
DManpb1-4DGlcpNAcb1-4DGlcpNAcb1-ROHGlycam Condensed SequenceGMML 1.0
WURCS=2.0/2,3,2/[a2122h-1b_1-5_2*NCC/3=O][a1122h-1b_1-5]/1-1-2/a4-b1_b4-c1WURCSPDB2Glycan 1.1.0
[][D-1-deoxy-GlcpNAc]{[(4+1)][b-D-GlcpNAc]{[(4+1)][b-D-Manp]{}}}LINUCSPDB-CARE

-
Non-polymers , 3 types, 618 molecules

#7: Chemical
ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 9 / Source method: obtained synthetically / Formula: Zn
#8: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: Cl
#9: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 606 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestN
Has protein modificationY

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.4 Å3/Da / Density % sol: 48.65 %
Crystal growTemperature: 293 K / Method: vapor diffusion / Details: 4 M Sodium Formate

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: ROTATING ANODE / Type: RIGAKU MICROMAX-007 / Wavelength: 1.54 Å
DetectorType: RIGAKU SATURN 944 / Detector: CCD / Date: Jan 25, 2018
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.54 Å / Relative weight: 1
ReflectionResolution: 2.3→50 Å / Num. obs: 57480 / % possible obs: 96 % / Redundancy: 2 % / Biso Wilson estimate: 27.4 Å2 / Rmerge(I) obs: 0.068 / Rpim(I) all: 0.068 / Rrim(I) all: 0.096 / Χ2: 0.886 / Net I/σ(I): 6.8 / Num. measured all: 112499
Reflection shell

Diffraction-ID: 1

Resolution (Å)Redundancy (%)Rmerge(I) obsNum. unique obsCC1/2Rpim(I) allRrim(I) allΧ2% possible all
2.3-2.341.90.31127880.820.3110.440.92592.6
2.34-2.381.90.27427410.8660.2740.3870.90293.6
2.38-2.431.90.2828470.8690.280.3960.85794.4
2.43-2.481.90.26528800.8710.2650.3740.89694.7
2.48-2.5320.24627820.90.2460.3480.89394.5
2.53-2.5920.22128980.9120.2210.3130.90695.3
2.59-2.6620.2128190.9150.210.2970.89995.1
2.66-2.7320.18428740.9370.1840.260.88395.5
2.73-2.8120.16928760.9420.1690.2390.91595.8
2.81-2.920.1528400.9540.150.2120.90196
2.9-320.12829220.9680.1280.1810.86796.4
3-3.1220.10428950.9780.1040.1470.93396.5
3.12-3.2620.07728580.9830.0770.1080.87796.7
3.26-3.4420.05929270.9880.0590.0840.84697
3.44-3.6520.04829390.9910.0480.0670.89497.4
3.65-3.9320.0428980.9950.040.0560.87497.7
3.93-4.3320.03429450.9960.0340.0480.80998
4.33-4.9520.03129610.9960.0310.0440.81198.2
4.95-6.2420.03529390.9960.0350.0490.86798.7
6.24-501.90.02728510.9970.0270.0390.97895.4

-
Processing

Software
NameVersionClassification
SCALEPACKdata scaling
PHENIX1.11.1_2575refinement
PDB_EXTRACT3.25data extraction
DENZOdata reduction
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 2AAI, 3EZJ
Resolution: 2.301→19.653 Å / SU ML: 0.26 / Cross valid method: THROUGHOUT / σ(F): 1.97 / Phase error: 25.38 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.2377 2742 4.77 %
Rwork0.187 54721 -
obs0.1894 57463 95.95 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso max: 147.07 Å2 / Biso mean: 40.9173 Å2 / Biso min: 12.51 Å2
Refinement stepCycle: final / Resolution: 2.301→19.653 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms9737 0 194 606 10537
Biso mean--58.05 38.13 -
Num. residues----1252
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00510165
X-RAY DIFFRACTIONf_angle_d0.86413849
X-RAY DIFFRACTIONf_chiral_restr0.0651582
X-RAY DIFFRACTIONf_plane_restr0.0051777
X-RAY DIFFRACTIONf_dihedral_angle_d5.3477093
Refine LS restraints NCS
Ens-IDDom-IDAuth asym-IDNumberRefine-IDRmsType
11A2440X-RAY DIFFRACTION8.294TORSIONAL
12D2440X-RAY DIFFRACTION8.294TORSIONAL
21B2432X-RAY DIFFRACTION8.294TORSIONAL
22E2432X-RAY DIFFRACTION8.294TORSIONAL
31C906X-RAY DIFFRACTION8.294TORSIONAL
32F906X-RAY DIFFRACTION8.294TORSIONAL
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Rfactor Rfree error: 0

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection Rwork% reflection obs (%)
2.301-2.34050.30081260.2316255790
2.3405-2.3830.30641110.2301264493
2.383-2.42870.28221090.2321273094
2.4287-2.47820.26541330.219275595
2.4782-2.5320.25771520.2175263294
2.532-2.59080.30351670.2093271695
2.5908-2.65540.30121440.218270095
2.6554-2.7270.27141650.2206267695
2.727-2.80710.28271350.205275996
2.8071-2.89740.26991700.2158269896
2.8974-3.00060.34481470.2193274596
3.0006-3.12030.29631390.2122274396
3.1203-3.26170.23811180.1896276797
3.2617-3.43280.23781440.178277397
3.4328-3.64660.18721320.1647280898
3.6466-3.92610.2019920.1617279397
3.9261-4.31740.20661240.1537281098
4.3174-4.93350.18251300.1523283098
4.9335-6.18340.23951490.1772280899
6.1834-19.6530.18471550.1847277798
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)
10.49981.50450.61447.23950.97542.3908-0.01120.0796-0.028-0.16510.03-0.5096-0.15190.3116-0.00870.1148-0.01130.01880.2289-0.00430.1836-40.01216.1019-73.3568
24.60510.92091.82915.1824-2.69483.317-0.03360.2378-0.0077-0.17120.02680.20410.05090.071-0.00890.1929-0.00510.00750.1708-0.02070.1136-51.78983.0828-81.0193
36.35260.7954-0.68473.3105-2.98434.9288-0.06550.6470.2724-0.40950.12240.3365-0.3239-0.0527-0.01870.38340.0126-0.09470.22470.00840.2058-55.996110.6338-85.8396
45.7017-1.7296-1.37635.83943.46058.44440.0269-0.0436-0.0658-0.3385-0.13170.60670.0117-0.52410.06680.1575-0.0744-0.01110.13340.02230.2343-60.8383-3.5543-73.5084
52.71071.51871.93192.39361.37663.4087-0.021-0.34420.0970.1654-0.11670.16490.0108-0.13020.13050.18320.01840.02930.1607-0.00990.1547-49.19725.46-60.1585
62.38930.5232-0.56383.85881.00641.5578-0.0095-0.06150.1794-0.1493-0.21750.4615-0.2169-0.33470.15740.23050.0161-0.03270.211-0.07130.2046-39.317420.7501-40.1214
74.51690.5962-0.66536.8892-0.80843.61960.0308-0.65290.56781.0583-0.32670.61910.0533-0.34690.27210.35720.01020.05540.3171-0.13090.2584-39.660223.1994-29.667
84.38130.99751.94185.00250.8433.3842-0.2269-0.16320.45290.2625-0.0133-0.0329-0.5232-0.14730.23910.28190.0034-0.02170.1827-0.06180.204-31.615929.5677-38.2536
92.88320.90970.52487.07795.65996.62960.0273-0.04880.1805-1.0479-0.0356-0.1083-0.7569-0.0044-0.00380.2920.0098-0.02660.15710.03210.2049-27.458523.7329-46.0036
101.35661.66940.90774.79282.11051.35390.1812-0.2488-0.11320.5529-0.0997-0.11010.1379-0.0691-0.06980.27340.017-0.03090.20530.01560.1425-32.386311.8069-39.387
116.2351-0.35985.12936.77222.46187.57830.4902-0.3456-0.52290.675-0.1405-0.45071.5469-0.0657-0.33190.3386-0.0004-0.04330.20720.0640.2796-35.9499-12.7329-47.2372
122.7550.45091.73248.65014.32778.06220.2904-0.6342-0.1690.9626-0.6420.66220.5256-0.67660.32870.2235-0.03120.03320.30190.0030.2075-40.0037-3.9694-40.6723
139.9539-1.3732-4.55666.18455.29916.01140.101-0.00250.05560.49430.487-1.20070.17770.5458-0.56350.42020.0267-0.11850.3030.06490.4373-23.0161-4.5501-44.4382
140.84171.0060.27195.37540.68444.96360.1098-0.1825-0.18960.46710.1061-0.22540.14590.0327-0.21680.12550.0296-0.02260.24340.00660.2105-29.63591.4814-45.0129
152.03991.66861.1518.80551.8944.6198-0.23540.2291-0.3403-0.22020.2549-0.49930.16080.1066-0.04620.19-0.0130.03070.1870.0130.195-29.178-5.9983-53.41
164.0073-1.41674.35437.7085-1.80718.52140.770.9145-2.1679-0.8572-0.3378-1.00660.78050.6198-0.43110.61910.02920.2310.5671-0.11571.4393-16.14-29.8456-65.7653
176.3603-0.57193.32327.2162-3.69189.4883-0.09670.9586-1.1782-1.0929-0.453-0.39481.63571.14040.4710.54490.09010.1510.5843-0.06280.6705-26.9632-22.0926-63.1002
189.1082-3.1210.83358.4926-1.50737.8064-0.28660.1964-0.8865-0.1394-0.1257-0.50920.4238-0.01830.35980.4243-0.04680.18040.3392-0.00890.5983-20.1943-18.3173-60.8733
198.1871-3.2684-2.04426.5488-0.72323.3052-0.34710.2903-2.07-0.1461-0.2853-0.75230.67740.30790.65990.6185-0.01930.15540.4598-0.00170.9748-22.2386-24.9206-59.2461
209.4264-8.2745-0.55872.01620.05232.7175-0.98820.5915-2.13670.0953-0.2454-0.50710.21430.21351.26830.7472-0.08050.25280.47280.07671.4884-24.1633-31.0058-60.0395
213.7917-0.04350.14486.0063.48112.8496-0.01870.05970.06110.03670.01390.70850.0396-0.31520.07940.19310.0074-0.01340.23030.04880.173-55.2127-40.983811.6027
222.4158-2.70781.89585.8931-1.36743.2113-0.1664-0.1498-0.030.49330.13820.1796-0.3184-0.19430.0170.1809-0.00720.02630.1903-0.01550.1532-52.6237-30.627312.6776
239.0066-4.62426.31917.7330.13126.5729-0.0085-0.06350.17970.05320.1827-0.37260.10890.0898-0.28150.2495-0.01690.05570.14030.00050.1632-41.1656-31.036417.8472
249.0703-1.016-3.29942.83614.02356.4263-0.0397-0.53910.10590.3834-0.0197-0.4097-0.32140.2008-0.06030.3993-0.0474-0.08130.2192-0.01230.2001-39.8455-28.050222.7325
257.2482-0.2990.13033.3071-3.58958.5448-0.1124-0.04270.1987-0.2056-0.0679-0.8283-0.360.68910.20710.11730.00750.03550.2437-0.00010.311-32.94-38.13383.5869
266.00930.56971.17095.7669-3.23168.327-0.0935-0.362-0.28050.7324-0.108-0.5098-0.08260.34250.09060.28040.0278-0.06080.14060.02170.2469-37.1592-46.315817.0351
274.79270.03533.36052.4294-0.43045.13080.1080.1912-0.225-0.13980.0653-0.11220.3685-0.0846-0.17050.2062-0.01190.03290.13410.00420.1466-44.645-41.15963.8426
283.1876-2.21792.39055.2886-3.47057.53440.02850.4388-0.3335-0.2845-0.01240.0460.43060.16890.05040.20330.06120.03770.2841-0.00780.2099-41.8174-40.4708-3.1025
295.982-1.75760.16355.05010.12815.3082-0.03980.51170.2806-0.3171-0.2453-0.31-0.46610.38030.29370.2516-0.0512-0.01710.2220.08940.2274-48.1308-25.7139-10.4158
303.24871.7958-0.00156.63576.43177.31440.11080.2886-0.0015-0.1172-0.27710.0836-0.1067-0.54190.10410.33830.0141-0.07430.24020.00540.1416-54.3894-23.5016-0.7591
312.8045-0.5025-0.64952.8144-1.68691.5347-0.061-0.02260.24060.2109-0.1142-0.4161-0.41090.270.1560.3574-0.0049-0.03650.22750.0710.2027-56.4746-17.8298-22.1912
324.3651-0.9311-0.18695.99390.21393.44680.09340.60190.4275-1.0021-0.491-0.73630.12350.35180.36420.42310.01530.04420.34250.15180.2737-56.1893-15.5736-33.478
332.9912-0.3860.67355.0139-1.26383.3275-0.02140.13510.2724-0.1908-0.06030.1904-0.27530.0670.06940.2098-0.0142-0.02790.15990.02990.1598-66.1139-13.2205-23.5103
340.1782-0.99820.42725.7316-2.43871.03430.11210.1614-0.0373-0.263-0.2117-0.0628-0.04670.18010.10150.2881-0.0147-0.02150.2031-0.01890.1206-61.3981-28.7762-20.9845
352.0033-1.29032.1335.713-2.5326.30220.21630.3849-0.202-0.919-0.3363-0.14380.70930.30510.11020.27610.01570.01840.2517-0.04550.1944-58.1094-45.7052-20.2722
360.4732-1.0270.55525.5839-0.4125.60160.1112-0.0924-0.2758-0.37320.05720.82570.3358-0.7486-0.13030.2206-0.0798-0.04340.3083-0.0230.2964-69.2503-39.2149-17.554
373.6815-1.35271.90158.4134-1.31613.5818-0.1273-0.017-0.56430.14810.22810.44520.1484-0.0607-0.07440.2176-0.0040.02030.1779-0.02840.1946-66.712-44.694-9.7411
383.4571.1149-3.96143.8819-2.56745.01170.1884-0.3213-1.83070.23960.01150.92920.329-0.608-0.20850.49130.01310.20540.48410.07411.369-79.73-68.63452.5829
396.04822.28983.78517.89996.24182.0073-0.6988-0.3873-1.13910.4892-0.35520.29210.9755-0.59631.05890.609-0.17610.22830.73260.08210.7736-69.1399-60.7486-0.5599
406.79713.17572.39174.8008-3.20716.6158-0.28640.4492-0.98350.09860.50520.24810.2463-0.2349-0.16380.432-0.03850.21010.4548-0.04680.6461-73.5262-56.8707-5.6351
417.13823.4144-1.01889.64761.53511.3028-0.306-0.2864-0.14650.215-0.65760.69330.4558-0.2840.95560.46680.0140.14640.4338-0.02970.675-77.871-57.2680.6315
429.85082.9383-0.08787.43491.69684.2797-0.61260.0807-2.0922-0.3819-0.43721.27730.3901-0.2831.02480.6687-0.11430.19890.586-0.0591.2307-79.0238-65.0429-3.2767
438.51846.9876-2.88089.5031-1.7773.6526-0.3659-0.4362-1.16670.0156-0.19860.09450.49760.16340.53370.6210.101-0.01710.3931-0.08380.7773-65.5387-65.6346-4.2841
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection detailsAuth asym-IDAuth seq-ID
1X-RAY DIFFRACTION1chain 'A' and (resid 5 through 56 )A5 - 56
2X-RAY DIFFRACTION2chain 'A' and (resid 57 through 97 )A57 - 97
3X-RAY DIFFRACTION3chain 'A' and (resid 98 through 122 )A98 - 122
4X-RAY DIFFRACTION4chain 'A' and (resid 123 through 160 )A123 - 160
5X-RAY DIFFRACTION5chain 'A' and (resid 161 through 261 )A161 - 261
6X-RAY DIFFRACTION6chain 'B' and (resid 3 through 26 )B3 - 26
7X-RAY DIFFRACTION7chain 'B' and (resid 27 through 47 )B27 - 47
8X-RAY DIFFRACTION8chain 'B' and (resid 48 through 84 )B48 - 84
9X-RAY DIFFRACTION9chain 'B' and (resid 85 through 103 )B85 - 103
10X-RAY DIFFRACTION10chain 'B' and (resid 104 through 145 )B104 - 145
11X-RAY DIFFRACTION11chain 'B' and (resid 146 through 162 )B146 - 162
12X-RAY DIFFRACTION12chain 'B' and (resid 163 through 188 )B163 - 188
13X-RAY DIFFRACTION13chain 'B' and (resid 189 through 201 )B189 - 201
14X-RAY DIFFRACTION14chain 'B' and (resid 202 through 223 )B202 - 223
15X-RAY DIFFRACTION15chain 'B' and (resid 224 through 262 )B224 - 262
16X-RAY DIFFRACTION16chain 'C' and (resid 3 through 24 )C3 - 24
17X-RAY DIFFRACTION17chain 'C' and (resid 25 through 38 )C25 - 38
18X-RAY DIFFRACTION18chain 'C' and (resid 44 through 77 )C44 - 77
19X-RAY DIFFRACTION19chain 'C' and (resid 78 through 108 )C78 - 108
20X-RAY DIFFRACTION20chain 'C' and (resid 109 through 120 )C109 - 120
21X-RAY DIFFRACTION21chain 'D' and (resid 5 through 32 )D5 - 32
22X-RAY DIFFRACTION22chain 'D' and (resid 33 through 75 )D33 - 75
23X-RAY DIFFRACTION23chain 'D' and (resid 76 through 97 )D76 - 97
24X-RAY DIFFRACTION24chain 'D' and (resid 98 through 122 )D98 - 122
25X-RAY DIFFRACTION25chain 'D' and (resid 123 through 140 )D123 - 140
26X-RAY DIFFRACTION26chain 'D' and (resid 141 through 160 )D141 - 160
27X-RAY DIFFRACTION27chain 'D' and (resid 161 through 194 )D161 - 194
28X-RAY DIFFRACTION28chain 'D' and (resid 195 through 210 )D195 - 210
29X-RAY DIFFRACTION29chain 'D' and (resid 211 through 247 )D211 - 247
30X-RAY DIFFRACTION30chain 'D' and (resid 248 through 262 )D248 - 262
31X-RAY DIFFRACTION31chain 'E' and (resid 2 through 26 )E2 - 26
32X-RAY DIFFRACTION32chain 'E' and (resid 27 through 47 )E27 - 47
33X-RAY DIFFRACTION33chain 'E' and (resid 48 through 118 )E48 - 118
34X-RAY DIFFRACTION34chain 'E' and (resid 119 through 145 )E119 - 145
35X-RAY DIFFRACTION35chain 'E' and (resid 146 through 192 )E146 - 192
36X-RAY DIFFRACTION36chain 'E' and (resid 193 through 223 )E193 - 223
37X-RAY DIFFRACTION37chain 'E' and (resid 224 through 262 )E224 - 262
38X-RAY DIFFRACTION38chain 'F' and (resid 3 through 24 )F3 - 24
39X-RAY DIFFRACTION39chain 'F' and (resid 25 through 38 )F25 - 38
40X-RAY DIFFRACTION40chain 'F' and (resid 44 through 60 )F44 - 60
41X-RAY DIFFRACTION41chain 'F' and (resid 61 through 77 )F61 - 77
42X-RAY DIFFRACTION42chain 'F' and (resid 78 through 100 )F78 - 100
43X-RAY DIFFRACTION43chain 'F' and (resid 101 through 120 )F101 - 120

+
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://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