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- PDB-8cwe: 20ns Temperature-Jump (Dark2) XFEL structure of Lysozyme Bound to... -

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Entry
Database: PDB / ID: 8cwe
Title20ns Temperature-Jump (Dark2) XFEL structure of Lysozyme Bound to N,N'-diacetylchitobiose
ComponentsLysozyme C
KeywordsHYDROLASE / lysozyme / temperature-jump / 20ns / dark2 / xfel / inhibitor / diacetylchitobiose
Function / homology
Function and homology information


Lactose synthesis / Antimicrobial peptides / Neutrophil degranulation / beta-N-acetylglucosaminidase activity / cell wall macromolecule catabolic process / lysozyme / lysozyme activity / defense response to Gram-negative bacterium / killing of cells of another organism / defense response to Gram-positive bacterium ...Lactose synthesis / Antimicrobial peptides / Neutrophil degranulation / beta-N-acetylglucosaminidase activity / cell wall macromolecule catabolic process / lysozyme / lysozyme activity / defense response to Gram-negative bacterium / killing of cells of another organism / defense response to Gram-positive bacterium / defense response to bacterium / endoplasmic reticulum / extracellular space / identical protein binding / cytoplasm
Similarity search - Function
Glycoside hydrolase, family 22, lysozyme / Glycoside hydrolase family 22 domain / Glycosyl hydrolases family 22 (GH22) domain signature. / Glycoside hydrolase, family 22 / C-type lysozyme/alpha-lactalbumin family / Glycosyl hydrolases family 22 (GH22) domain profile. / Alpha-lactalbumin / lysozyme C / Lysozyme-like domain superfamily
Similarity search - Domain/homology
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 1.48 Å
AuthorsWolff, A.M. / Thompson, M.C. / Fraser, J.S. / Nango, E.
Funding support United States, 2items
OrganizationGrant numberCountry
National Science Foundation (NSF, United States)1231306 United States
Department of Energy (DOE, United States)DE-AC02-76SF00515 United States
Citation
Journal: Nat.Chem. / Year: 2023
Title: Mapping protein dynamics at high spatial resolution with temperature-jump X-ray crystallography.
Authors: Wolff, A.M. / Nango, E. / Young, I.D. / Brewster, A.S. / Kubo, M. / Nomura, T. / Sugahara, M. / Owada, S. / Barad, B.A. / Ito, K. / Bhowmick, A. / Carbajo, S. / Hino, T. / Holton, J.M. / Im, ...Authors: Wolff, A.M. / Nango, E. / Young, I.D. / Brewster, A.S. / Kubo, M. / Nomura, T. / Sugahara, M. / Owada, S. / Barad, B.A. / Ito, K. / Bhowmick, A. / Carbajo, S. / Hino, T. / Holton, J.M. / Im, D. / O'Riordan, L.J. / Tanaka, T. / Tanaka, R. / Sierra, R.G. / Yumoto, F. / Tono, K. / Iwata, S. / Sauter, N.K. / Fraser, J.S. / Thompson, M.C.
#1: Journal: Biorxiv / Year: 2022
Title: Mapping Protein Dynamics at High-Resolution with Temperature-Jump X-ray Crystallography
Authors: Wolff, A.M. / Nango, E. / Young, I.D. / Brewster, A.S. / Kubo, M. / Nomura, T. / Sugahara, M. / Owada, S. / Barad, B.A. / Ito, K. / Bhowmick, A. / Carbajo, S. / Hino, T. / Holton, J.M. / Im, ...Authors: Wolff, A.M. / Nango, E. / Young, I.D. / Brewster, A.S. / Kubo, M. / Nomura, T. / Sugahara, M. / Owada, S. / Barad, B.A. / Ito, K. / Bhowmick, A. / Carbajo, S. / Hino, T. / Holton, J.M. / Im, D. / O'Riordan, L.J. / Tanaka, T. / Tanaka, R. / Sierra, R.G. / Yumoto, F. / Tono, K. / Iwata, S. / Sauter, N.K. / Fraser, J.S. / Thompson, M.C.
History
DepositionMay 19, 2022Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jun 22, 2022Provider: repository / Type: Initial release
Revision 2.0Jan 25, 2023Group: Atomic model / Author supporting evidence ...Atomic model / Author supporting evidence / Data collection / Database references / Derived calculations / Non-polymer description / Structure summary
Category: atom_site / atom_site_anisotrop ...atom_site / atom_site_anisotrop / chem_comp / citation / entity / pdbx_branch_scheme / pdbx_chem_comp_identifier / pdbx_entity_branch / pdbx_entity_branch_descriptor / pdbx_entity_branch_link / pdbx_entity_branch_list / pdbx_entity_instance_feature / pdbx_entity_nonpoly / pdbx_nonpoly_scheme / pdbx_struct_conn_angle / pdbx_struct_special_symmetry / struct_asym / struct_conn / struct_conn_type
Item: _atom_site.B_iso_or_equiv / _atom_site.Cartn_x ..._atom_site.B_iso_or_equiv / _atom_site.Cartn_x / _atom_site.Cartn_y / _atom_site.Cartn_z / _atom_site.auth_asym_id / _atom_site.auth_atom_id / _atom_site.auth_comp_id / _atom_site.auth_seq_id / _atom_site.label_asym_id / _atom_site.label_atom_id / _atom_site.label_comp_id / _atom_site.label_entity_id / _atom_site.occupancy / _atom_site.type_symbol / _atom_site_anisotrop.U[1][1] / _atom_site_anisotrop.U[1][2] / _atom_site_anisotrop.U[1][3] / _atom_site_anisotrop.U[2][2] / _atom_site_anisotrop.U[2][3] / _atom_site_anisotrop.U[3][3] / _atom_site_anisotrop.id / _atom_site_anisotrop.pdbx_auth_asym_id / _atom_site_anisotrop.pdbx_auth_atom_id / _atom_site_anisotrop.pdbx_auth_comp_id / _atom_site_anisotrop.pdbx_auth_seq_id / _atom_site_anisotrop.pdbx_label_asym_id / _atom_site_anisotrop.pdbx_label_atom_id / _atom_site_anisotrop.pdbx_label_comp_id / _atom_site_anisotrop.type_symbol / _chem_comp.formula / _chem_comp.formula_weight / _chem_comp.id / _chem_comp.mon_nstd_flag / _chem_comp.name / _chem_comp.pdbx_synonyms / _chem_comp.type / _citation.journal_id_ISSN / _entity.formula_weight / _entity.pdbx_description / _entity.pdbx_number_of_molecules / _entity.type / _pdbx_struct_conn_angle.ptnr1_auth_asym_id / _pdbx_struct_conn_angle.ptnr1_auth_comp_id / _pdbx_struct_conn_angle.ptnr1_auth_seq_id / _pdbx_struct_conn_angle.ptnr1_label_asym_id / _pdbx_struct_conn_angle.ptnr1_label_atom_id / _pdbx_struct_conn_angle.ptnr1_label_comp_id / _pdbx_struct_conn_angle.ptnr2_auth_seq_id / _pdbx_struct_conn_angle.ptnr2_label_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_comp_id / _pdbx_struct_conn_angle.ptnr3_auth_seq_id / _pdbx_struct_conn_angle.ptnr3_label_asym_id / _pdbx_struct_conn_angle.ptnr3_label_atom_id / _pdbx_struct_conn_angle.ptnr3_label_comp_id / _pdbx_struct_conn_angle.value / _pdbx_struct_special_symmetry.auth_seq_id / _struct_asym.entity_id
Revision 2.1Aug 16, 2023Group: Data collection / Database references
Category: chem_comp_atom / chem_comp_bond / pdbx_related_exp_data_set
Revision 2.2Oct 4, 2023Group: Database references / Category: citation / citation_author
Revision 2.3Oct 25, 2023Group: Refinement description / Category: pdbx_initial_refinement_model
Revision 2.4Nov 15, 2023Group: Database references / Category: citation
Item: _citation.journal_volume / _citation.page_first / _citation.page_last
Revision 2.5Oct 23, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Lysozyme C
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,9799
Polymers14,3311
Non-polymers6488
Water1,71195
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)77.061, 77.061, 37.223
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number96
Space group name H-MP43212
Space group name HallP4nw2abw
Components on special symmetry positions
IDModelComponents
11A-301-

HOH

21A-350-

HOH

31A-370-

HOH

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Components

#1: Protein Lysozyme C / 1 / 4-beta-N-acetylmuramidase C / Allergen Gal d IV


Mass: 14331.160 Da / Num. of mol.: 1 / Fragment: lyzozyme / Source method: obtained synthetically / Source: (synth.) Gallus gallus (chicken) / References: UniProt: P00698, lysozyme
#2: Polysaccharide 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose


Type: oligosaccharide / Mass: 424.401 Da / Num. of mol.: 1 / Source method: obtained synthetically
DescriptorTypeProgram
DGlcpNAcb1-4DGlcpNAca1-ROHGlycam Condensed SequenceGMML 1.0
WURCS=2.0/2,2,1/[a2122h-1a_1-5_2*NCC/3=O][a2122h-1b_1-5_2*NCC/3=O]/1-2/a4-b1WURCSPDB2Glycan 1.1.0
[][a-D-GlcpNAc]{[(4+1)][b-D-GlcpNAc]{}}LINUCSPDB-CARE
#3: Chemical ChemComp-NA / SODIUM ION


Mass: 22.990 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Na
#4: Chemical
ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 5 / Source method: isolated from a natural source / Formula: Cl
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 95 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestY
Has protein modificationY

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Experimental details

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Experiment

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

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Sample preparation

CrystalDensity Matthews: 1.93 Å3/Da / Density % sol: 36.2 %
Crystal growTemperature: 291 K / Method: batch mode / pH: 3
Details: Lysozyme-inhibitor complex [20 mg/ml lysozyme plus 10 mg/ml N,N'-diacetylchitobiose dissolved in 0.1 M sodium acetate at pH 3.0] mixed with precipitant [28% (w/v) NaCl, 8% (w/v) PEG6000 and ...Details: Lysozyme-inhibitor complex [20 mg/ml lysozyme plus 10 mg/ml N,N'-diacetylchitobiose dissolved in 0.1 M sodium acetate at pH 3.0] mixed with precipitant [28% (w/v) NaCl, 8% (w/v) PEG6000 and 0.1 M sodium acetate at pH 3.0] in a 1:1 ratio

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Data collection

DiffractionMean temperature: 291 K / Serial crystal experiment: Y
Diffraction sourceSource: FREE ELECTRON LASER / Site: SACLA / Beamline: BL3 / Wavelength: 1.2468 Å
DetectorType: MPCCD / Detector: CCD / Date: Jul 24, 2018
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.2468 Å / Relative weight: 1
ReflectionResolution: 1.48→30.74 Å / Num. obs: 3127348 / % possible obs: 99.98 % / Redundancy: 162.5 % / Biso Wilson estimate: 15.32 Å2 / CC1/2: 0.994 / Net I/σ(I): 11.287
Reflection shellResolution: 1.48→1.51 Å / Num. unique obs: 31601 / CC1/2: 0.823
Serial crystallography sample deliveryMethod: injection

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Processing

Software
NameVersionClassification
PHENIX1.19.2_4158refinement
PDB_EXTRACT3.27data extraction
cctbx.xfeldata reduction
cxi.mergedata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 1iee

1iee


Resolution: 1.48→30.74 Å / SU ML: 0.1015 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 15.3835
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.1624 984 5.11 %
Rwork0.1291 18261 -
obs0.1308 19245 100 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 19.57 Å2
Refinement stepCycle: LAST / Resolution: 1.48→30.74 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1001 0 36 95 1132
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0191084
X-RAY DIFFRACTIONf_angle_d1.26451473
X-RAY DIFFRACTIONf_chiral_restr0.084158
X-RAY DIFFRACTIONf_plane_restr0.0114191
X-RAY DIFFRACTIONf_dihedral_angle_d12.5397390
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.48-1.560.19821410.1082556X-RAY DIFFRACTION100
1.56-1.660.14471280.09362548X-RAY DIFFRACTION100
1.66-1.780.1591390.10262594X-RAY DIFFRACTION100
1.78-1.960.13531490.09732557X-RAY DIFFRACTION100
1.96-2.250.14231530.10332569X-RAY DIFFRACTION100
2.25-2.830.1651290.13272657X-RAY DIFFRACTION100
2.83-30.740.17671450.15742780X-RAY DIFFRACTION100

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