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- PDB-1ql0: Sm Endonuclease from Seratia marcenscens at atomic resolution -

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Basic information

Entry
Database: PDB / ID: 1ql0
TitleSm Endonuclease from Seratia marcenscens at atomic resolution
ComponentsNUCLEASE
KeywordsHYDROLASE / ENDONUCLEASE / NUCLEASE
Function / homology
Function and homology information


Serratia marcescens nuclease / single-stranded DNA endodeoxyribonuclease activity / RNA endonuclease activity / nucleic acid binding / extracellular region / metal ion binding
Similarity search - Function
DNA/RNA non-specific endonuclease, active site / DNA/RNA non-specific endonucleases active site. / Non-specific endonuclease / Extracellular Endonuclease; Chain A / Extracellular Endonuclease, subunit A / Extracellular Endonuclease, subunit A / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease ...DNA/RNA non-specific endonuclease, active site / DNA/RNA non-specific endonucleases active site. / Non-specific endonuclease / Extracellular Endonuclease; Chain A / Extracellular Endonuclease, subunit A / Extracellular Endonuclease, subunit A / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease / DNA/RNA non-specific endonuclease superfamily / His-Me finger superfamily / 3-Layer(aba) Sandwich / Alpha Beta
Similarity search - Domain/homology
Biological speciesSERRATIA MARCESCENS (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.1 Å
AuthorsPerbandt, M. / Mikhailov, A.M. / Betzel, C.H.
CitationJournal: Acta Crystallogr.,Sect.D / Year: 2000
Title: Atomic Structure of the Serratia Marcescens Endonuclease at 1.1 A Resolution and the Enzyme Reaction Mechanism.
Authors: Shlyapnikov, S.V. / Lunin, V.V. / Perbandt, M. / Polyakov, K.M. / Lunin, V.Y. / Levdikov, V.M. / Betzel, C. / Mikhailov, A.M.
History
DepositionAug 18, 1999Deposition site: PDBE / Processing site: PDBE
Revision 1.0May 7, 2000Provider: repository / Type: Initial release
Revision 1.1Mar 12, 2014Group: Database references / Derived calculations ...Database references / Derived calculations / Non-polymer description / Other / Source and taxonomy / Structure summary / Version format compliance
Revision 1.2Jul 24, 2019Group: Data collection / Category: diffrn_source / Item: _diffrn_source.pdbx_synchrotron_site

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: NUCLEASE
B: NUCLEASE
hetero molecules


Theoretical massNumber of molelcules
Total (without water)52,6404
Polymers52,5912
Non-polymers492
Water15,061836
1


  • Idetical with deposited unit
  • defined by software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area2020 Å2
ΔGint-22 kcal/mol
Surface area18610 Å2
MethodPISA
Unit cell
Length a, b, c (Å)106.390, 73.670, 68.120
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number18
Space group name H-MP21212

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Components

#1: Protein NUCLEASE / ENDONUCLEASE


Mass: 26295.508 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Details: MG BINDING SITE AT RESIDUE 127 / Source: (gene. exp.) SERRATIA MARCESCENS (bacteria) / Production host: SERRATIA MARCESCENS (bacteria) / References: UniProt: P13717, Serratia marcescens nuclease
#2: Chemical ChemComp-MG / MAGNESIUM ION


Mass: 24.305 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Mg
#3: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 836 / Source method: isolated from a natural source / Formula: H2O

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION

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Sample preparation

CrystalDensity Matthews: 2.54 Å3/Da / Density % sol: 51.54 %
Crystal growpH: 6.5 / Details: pH 6.50
Crystal grow
*PLUS
Method: other / Details: Bannikova, G.E., (1991) Biochem. Int., 23, 813.

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Data collection

DiffractionMean temperature: 120 K
Diffraction sourceSource: SYNCHROTRON / Site: EMBL/DESY, HAMBURG / Beamline: BW7B / Wavelength: 1
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 1.1→20 Å / Num. obs: 216595 / % possible obs: 91.5 % / Redundancy: 3.4 % / Rsym value: 0.041
Reflection
*PLUS
Num. obs: 198103 / Rmerge(I) obs: 0.041
Reflection shell
*PLUS
Rmerge(I) obs: 0.252

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Processing

Software
NameClassification
SHELXL-97refinement
SHELXL-97phasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.1→20 Å / Cross valid method: THROUGHOUT / σ(F): 0
RfactorNum. reflection% reflectionSelection details
Rfree0.147 10828 5 %EVERY 20TH REFLECTION
obs0.128 -91.5 %-
all-216595 --
Refinement stepCycle: LAST / Resolution: 1.1→20 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms3703 0 2 836 4541
Refine LS restraints
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONs_bond_d0.023
X-RAY DIFFRACTIONs_angle_d0.041
X-RAY DIFFRACTIONs_similar_dist
X-RAY DIFFRACTIONs_from_restr_planes
X-RAY DIFFRACTIONs_zero_chiral_vol
X-RAY DIFFRACTIONs_non_zero_chiral_vol
X-RAY DIFFRACTIONs_anti_bump_dis_restr
X-RAY DIFFRACTIONs_rigid_bond_adp_cmpnt
X-RAY DIFFRACTIONs_similar_adp_cmpnt
X-RAY DIFFRACTIONs_approx_iso_adps
Refinement
*PLUS
Num. reflection obs: 184483 / Rfactor obs: 0.129 / Rfactor Rfree: 0.156 / Rfactor Rwork: 0.147
Solvent computation
*PLUS
Displacement parameters
*PLUS
Refine LS restraints
*PLUS
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONs_dihedral_angle_d
X-RAY DIFFRACTIONs_dihedral_angle_deg4.5
X-RAY DIFFRACTIONs_chiral_restr0.113

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