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- PDB-8qxz: Xylanase from Bacillus circulans mutant E78Q/Y69A -

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Basic information

Entry
Database: PDB / ID: 8qxz
TitleXylanase from Bacillus circulans mutant E78Q/Y69A
ComponentsEndo-1,4-beta-xylanase
KeywordsHYDROLASE
Function / homology
Function and homology information


endo-1,4-beta-xylanase activity / endo-1,4-beta-xylanase / xylan catabolic process
Similarity search - Function
Glycoside hydrolase family 11, active site 2 / Glycosyl hydrolases family 11 (GH11) active site signature 2. / Glycoside hydrolase family 11, active site 1 / Glycosyl hydrolases family 11 (GH11) active site signature 1. / Glycoside hydrolase family 11 / Glycosyl hydrolases family 11 (GH11) domain / Glycosyl hydrolases family 11 / Glycosyl hydrolases family 11 (GH11) domain profile. / Glycoside hydrolase family 11/12 / Concanavalin A-like lectin/glucanase domain superfamily
Similarity search - Domain/homology
DI(HYDROXYETHYL)ETHER / Endo-1,4-beta-xylanase
Similarity search - Component
Biological speciesNiallia circulans subsp. circulans (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.5 Å
AuthorsChikunova, A. / Saberi, M. / Ubbink, M.
Funding support Netherlands, 1items
OrganizationGrant numberCountry
Netherlands Organisation for Scientific Research (NWO) Netherlands
CitationJournal: Febs J. / Year: 2024
Title: Bimodal substrate binding in the active site of the glycosidase BcX.
Authors: Saberi, M. / Chikunova, A. / Ben Bdira, F. / Cramer-Blok, A. / Timmer, M. / Voskamp, P. / Ubbink, M.
History
DepositionOct 25, 2023Deposition site: PDBE / Processing site: PDBE
Revision 1.0Aug 21, 2024Provider: repository / Type: Initial release
Revision 1.1Sep 4, 2024Group: Database references / Category: citation / citation_author / Item: _citation.pdbx_database_id_PubMed / _citation.title
Revision 1.2Oct 16, 2024Group: Database references / Structure summary / Category: citation / pdbx_entry_details
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _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: Endo-1,4-beta-xylanase
B: Endo-1,4-beta-xylanase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)41,4719
Polymers40,6322
Non-polymers8407
Water6,900383
1
A: Endo-1,4-beta-xylanase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)20,7895
Polymers20,3161
Non-polymers4734
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
B: Endo-1,4-beta-xylanase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)20,6834
Polymers20,3161
Non-polymers3673
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)79.345, 79.345, 133.171
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number96
Space group name H-MP43212

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Components

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Protein , 1 types, 2 molecules AB

#1: Protein Endo-1,4-beta-xylanase


Mass: 20315.924 Da / Num. of mol.: 2 / Mutation: E78Q, Y69A
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Niallia circulans subsp. circulans (bacteria)
Gene: xlnA / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: P09850

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Non-polymers , 5 types, 390 molecules

#2: Chemical ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Formula: Zn
#3: Chemical ChemComp-BTB / 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL / BIS-TRIS BUFFER


Mass: 209.240 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C8H19NO5 / Comment: pH buffer*YM
#4: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL


Mass: 92.094 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C3H8O3
#5: Chemical ChemComp-PEG / DI(HYDROXYETHYL)ETHER


Mass: 106.120 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C4H10O3
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 383 / Source method: isolated from a natural source / Formula: H2O

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Details

Has ligand of interestN
Has protein modificationN

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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: 2.58 Å3/Da / Density % sol: 52.31 %
Crystal growTemperature: 291 K / Method: vapor diffusion, sitting drop / pH: 7.5 / Details: 10 %v/v PEGSB, 0.2 M LiSO4, BIS-TRIS, pH 7.5

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: Diamond / Beamline: I04 / Wavelength: 0.9795 Å
DetectorType: DECTRIS PILATUS 2M / Detector: PIXEL / Date: Nov 26, 2021
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9795 Å / Relative weight: 1
ReflectionResolution: 1.5→68.26 Å / Num. obs: 68694 / % possible obs: 100 % / Redundancy: 1.9 % / CC1/2: 0.999 / Net I/σ(I): 13.2
Reflection shellResolution: 1.5→1.53 Å / Num. unique obs: 3352 / CC1/2: 0.849

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Processing

Software
NameVersionClassification
REFMAC5.8.0411refinement
XDSdata reduction
Aimlessdata scaling
MOLREPphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.5→68.26 Å / Cor.coef. Fo:Fc: 0.977 / Cor.coef. Fo:Fc free: 0.961 / SU B: 1.34 / SU ML: 0.047 / Cross valid method: THROUGHOUT / ESU R: 0.059 / ESU R Free: 0.063 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.1832 3356 4.9 %RANDOM
Rwork0.15379 ---
obs0.15522 65327 99.98 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK
Displacement parametersBiso mean: 19.116 Å2
Baniso -1Baniso -2Baniso -3
1-1.05 Å2-0 Å2-0 Å2
2--1.05 Å2-0 Å2
3----2.11 Å2
Refinement stepCycle: 1 / Resolution: 1.5→68.26 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2882 0 49 383 3314
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.010.0113047
X-RAY DIFFRACTIONr_bond_other_d0.0010.0162589
X-RAY DIFFRACTIONr_angle_refined_deg1.5581.6544172
X-RAY DIFFRACTIONr_angle_other_deg0.5351.5655919
X-RAY DIFFRACTIONr_dihedral_angle_1_deg8.3535372
X-RAY DIFFRACTIONr_dihedral_angle_2_deg6.921514
X-RAY DIFFRACTIONr_dihedral_angle_3_deg11.55510390
X-RAY DIFFRACTIONr_dihedral_angle_4_deg
X-RAY DIFFRACTIONr_chiral_restr0.0720.2431
X-RAY DIFFRACTIONr_gen_planes_refined0.0110.023648
X-RAY DIFFRACTIONr_gen_planes_other0.0010.02816
X-RAY DIFFRACTIONr_nbd_refined
X-RAY DIFFRACTIONr_nbd_other
X-RAY DIFFRACTIONr_nbtor_refined
X-RAY DIFFRACTIONr_nbtor_other
X-RAY DIFFRACTIONr_xyhbond_nbd_refined
X-RAY DIFFRACTIONr_xyhbond_nbd_other
X-RAY DIFFRACTIONr_metal_ion_refined
X-RAY DIFFRACTIONr_metal_ion_other
X-RAY DIFFRACTIONr_symmetry_vdw_refined
X-RAY DIFFRACTIONr_symmetry_vdw_other
X-RAY DIFFRACTIONr_symmetry_hbond_refined
X-RAY DIFFRACTIONr_symmetry_hbond_other
X-RAY DIFFRACTIONr_symmetry_metal_ion_refined
X-RAY DIFFRACTIONr_symmetry_metal_ion_other
X-RAY DIFFRACTIONr_mcbond_it1.8141.9511488
X-RAY DIFFRACTIONr_mcbond_other1.8131.9511488
X-RAY DIFFRACTIONr_mcangle_it2.5843.4931860
X-RAY DIFFRACTIONr_mcangle_other2.5843.4941861
X-RAY DIFFRACTIONr_scbond_it3.2132.1751559
X-RAY DIFFRACTIONr_scbond_other3.2122.1761560
X-RAY DIFFRACTIONr_scangle_it
X-RAY DIFFRACTIONr_scangle_other4.1283.8742313
X-RAY DIFFRACTIONr_long_range_B_refined5.18622.853605
X-RAY DIFFRACTIONr_long_range_B_other4.98820.853515
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 1.5→1.539 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.28 223 -
Rwork0.266 4776 -
obs--99.96 %

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