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- PDB-4etc: Lysozyme, room temperature, 24 kGy dose -

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Basic information

Entry
Database: PDB / ID: 4etc
TitleLysozyme, room temperature, 24 kGy dose
ComponentsLysozyme C
KeywordsHYDROLASE / lysozyme
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
Lysozyme - #10 / 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 / Lysozyme-like domain superfamily ...Lysozyme - #10 / 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 / Lysozyme-like domain superfamily / Orthogonal Bundle / Mainly Alpha
Similarity search - Domain/homology
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / SYNCHROTRON / FOURIER SYNTHESIS / Resolution: 1.906 Å
AuthorsBoutet, S. / Lomb, L. / Williams, G. / Barends, T. / Aquila, A. / Doak, R.B. / Weierstall, U. / DePonte, D. / Steinbrener, J. / Shoeman, R. ...Boutet, S. / Lomb, L. / Williams, G. / Barends, T. / Aquila, A. / Doak, R.B. / Weierstall, U. / DePonte, D. / Steinbrener, J. / Shoeman, R. / Messerschmidt, M. / Barty, A. / White, T. / Kassemeyer, S. / Kirian, R. / Seibert, M. / Montanez, P. / Kenney, C. / Herbst, R. / Hart, P. / Pines, J. / Haller, G. / Gruner, S. / Philllip, H. / Tate, M. / Hromalik, M. / Koerner, L. / van Bakel, N. / Morse, J. / Ghonsalves, W. / Arnlund, D. / Bogan, M. / Calemann, C. / Fromme, R. / Hampton, C. / Hunter, M. / Johansson, L. / Katona, G. / Kupitz, C. / Liang, M. / Martin, A. / Nass, K. / Redecke, L. / Stellato, F. / Timneanu, N. / Wang, D. / Zatsepin, N. / Schafer, D. / Defever, K. / Neutze, R. / Fromme, P. / Spence, J. / Chapman, H. / Schlichting, I.
CitationJournal: Science / Year: 2012
Title: High-resolution protein structure determination by serial femtosecond crystallography.
Authors: Boutet, S. / Lomb, L. / Williams, G.J. / Barends, T.R. / Aquila, A. / Doak, R.B. / Weierstall, U. / DePonte, D.P. / Steinbrener, J. / Shoeman, R.L. / Messerschmidt, M. / Barty, A. / White, T. ...Authors: Boutet, S. / Lomb, L. / Williams, G.J. / Barends, T.R. / Aquila, A. / Doak, R.B. / Weierstall, U. / DePonte, D.P. / Steinbrener, J. / Shoeman, R.L. / Messerschmidt, M. / Barty, A. / White, T.A. / Kassemeyer, S. / Kirian, R.A. / Seibert, M.M. / Montanez, P.A. / Kenney, C. / Herbst, R. / Hart, P. / Pines, J. / Haller, G. / Gruner, S.M. / Philipp, H.T. / Tate, M.W. / Hromalik, M. / Koerner, L.J. / van Bakel, N. / Morse, J. / Ghonsalves, W. / Arnlund, D. / Bogan, M.J. / Caleman, C. / Fromme, R. / Hampton, C.Y. / Hunter, M.S. / Johansson, L.C. / Katona, G. / Kupitz, C. / Liang, M. / Martin, A.V. / Nass, K. / Redecke, L. / Stellato, F. / Timneanu, N. / Wang, D. / Zatsepin, N.A. / Schafer, D. / Defever, J. / Neutze, R. / Fromme, P. / Spence, J.C. / Chapman, H.N. / Schlichting, I.
History
DepositionApr 24, 2012Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jun 13, 2012Provider: repository / Type: Initial release
Revision 1.1Aug 8, 2012Group: Database references
Revision 1.2Nov 15, 2017Group: Refinement description / Category: software
Revision 1.3Nov 20, 2024Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Structure summary
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_entry_details / pdbx_modification_feature / pdbx_struct_conn_angle / struct_conn / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_struct_conn_angle.ptnr1_auth_comp_id / _pdbx_struct_conn_angle.ptnr1_auth_seq_id / _pdbx_struct_conn_angle.ptnr1_label_atom_id / _pdbx_struct_conn_angle.ptnr1_label_comp_id / _pdbx_struct_conn_angle.ptnr1_label_seq_id / _pdbx_struct_conn_angle.ptnr3_auth_comp_id / _pdbx_struct_conn_angle.ptnr3_auth_seq_id / _pdbx_struct_conn_angle.ptnr3_label_atom_id / _pdbx_struct_conn_angle.ptnr3_label_comp_id / _pdbx_struct_conn_angle.ptnr3_label_seq_id / _pdbx_struct_conn_angle.value / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_comp_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_atom_id / _struct_conn.ptnr1_label_comp_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_seq_id / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Lysozyme C
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,3903
Polymers14,3311
Non-polymers582
Water1,40578
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)79.290, 79.290, 38.120
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number96
Space group name H-MP43212
Components on special symmetry positions
IDModelComponents
11A-378-

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 / Source method: isolated from a natural source / Source: (natural) Gallus gallus (chicken) / References: UniProt: P00698, lysozyme
#2: Chemical ChemComp-NA / SODIUM ION


Mass: 22.990 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Na
#3: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Cl
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 78 / Source method: isolated from a natural source / Formula: H2O
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: 2.09 Å3/Da / Density % sol: 41.16 %
Crystal growTemperature: 293 K / Method: vapor diffusion
Details: grown in Linbro plates in hanging or sitting drop geometry. Drops of equal volume of protein (20 mg/ml) and reservoir solution (1 M NaAc pH 3.0, 9-10 % NaCl, 6 % PEG 6000) were mixed. For ...Details: grown in Linbro plates in hanging or sitting drop geometry. Drops of equal volume of protein (20 mg/ml) and reservoir solution (1 M NaAc pH 3.0, 9-10 % NaCl, 6 % PEG 6000) were mixed. For the measurements, the crystals were equilibrated in 1 M NaAc pH 3.4, 10 % NaCl, VAPOR DIFFUSION, temperature 293K

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Data collection

DiffractionMean temperature: 293 K
Diffraction sourceSource: SYNCHROTRON / Site: SLS / Beamline: X10SA / Wavelength: 0.9997 Å
DetectorType: PSI PILATUS 6M / Detector: PIXEL / Date: Mar 25, 2012
RadiationMonochromator: SI111 / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9997 Å / Relative weight: 1
ReflectionResolution: 1.9→35.4 Å / Num. all: 9297 / Num. obs: 9297 / % possible obs: 92.6 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0
Reflection shellResolution: 1.9→2 Å / % possible all: 95.1

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Processing

Software
NameVersionClassification
PHENIXmodel building
PHENIX(phenix.refine: 1.7.2_869)refinement
XDSdata reduction
XDSdata scaling
PHENIXphasing
RefinementMethod to determine structure: FOURIER SYNTHESIS / Resolution: 1.906→35.4 Å / SU ML: 0.29 / σ(F): 1.36 / σ(I): 0 / Phase error: 18.48 / Stereochemistry target values: ML
RfactorNum. reflection% reflectionSelection details
Rfree0.2001 466 5.07 %RANDOM
Rwork0.1661 ---
obs0.1678 9193 92.62 %-
all-9193 --
Solvent computationShrinkage radii: 0.98 Å / VDW probe radii: 1.2 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 34.381 Å2 / ksol: 0.337 e/Å3
Displacement parameters
Baniso -1Baniso -2Baniso -3
1--0.5815 Å2-0 Å20 Å2
2---0.5815 Å20 Å2
3---1.1631 Å2
Refinement stepCycle: LAST / Resolution: 1.906→35.4 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1001 0 2 78 1081
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0071025
X-RAY DIFFRACTIONf_angle_d1.0481381
X-RAY DIFFRACTIONf_dihedral_angle_d13.875365
X-RAY DIFFRACTIONf_chiral_restr0.081144
X-RAY DIFFRACTIONf_plane_restr0.003181
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.906-2.18230.20491570.17132884X-RAY DIFFRACTION95
2.1823-2.74930.2071570.15662912X-RAY DIFFRACTION93
2.7493-35.46570.19481520.16912931X-RAY DIFFRACTION90

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