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- PDB-1rh0: Crystal structure of human Tyrosyl-DNA Phosphodiesterase complexe... -

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Basic information

Entry
Database: PDB / ID: 1rh0
TitleCrystal structure of human Tyrosyl-DNA Phosphodiesterase complexed with vanadate, octopamine and trinucleotide GTT
Components
  • 5'-D(*GP*TP*T)-3'
  • Tyrosyl-DNA phosphodiesterase 1
KeywordsHYDROLASE/DNA / protein-DNA complex / vanadate complex / transition state mimic / HYDROLASE-DNA COMPLEX
Function / homology
Function and homology information


3'-tyrosyl-DNA phosphodiesterase activity / single strand break repair / Hydrolases; Acting on ester bonds; Phosphoric-diester hydrolases / exonuclease activity / Nonhomologous End-Joining (NHEJ) / double-strand break repair / single-stranded DNA binding / double-stranded DNA binding / intracellular membrane-bounded organelle / DNA repair ...3'-tyrosyl-DNA phosphodiesterase activity / single strand break repair / Hydrolases; Acting on ester bonds; Phosphoric-diester hydrolases / exonuclease activity / Nonhomologous End-Joining (NHEJ) / double-strand break repair / single-stranded DNA binding / double-stranded DNA binding / intracellular membrane-bounded organelle / DNA repair / nucleoplasm / nucleus / plasma membrane / cytoplasm
Similarity search - Function
Tyrosyl-DNA phosphodiesterase I / Tyrosyl-DNA phosphodiesterase / Endonuclease Chain A / Endonuclease; Chain A / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
4-(2S-AMINO-1-HYDROXYETHYL)PHENOL / SPERMINE / VANADATE ION / DNA / Tyrosyl-DNA phosphodiesterase 1
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.3 Å
AuthorsDavies, D.R. / Interthal, H. / Champoux, J.J. / Hol, W.G.
Citation
Journal: J.Med.Chem. / Year: 2004
Title: Explorations of peptide and oligonucleotide binding sites of tyrosyl-DNA phosphodiesterase using vanadate complexes.
Authors: Davies, D.R. / Interthal, H. / Champoux, J.J. / Hol, W.G.
#1: Journal: Chem.Biol. / Year: 2003
Title: Crystal structure of a transition state mimic for Tdp1 assembled from vanadate, DNA, and a topoisomerase I-derived peptide
Authors: Davies, D.R. / Interthal, H. / Champoux, J.J. / Hol, W.G.J.
#2: Journal: J.Mol.Biol. / Year: 2002
Title: Insights into substrate binding and catalytic mechanism of human Tyrosyl-DNA Phosphodiesterase (Tdp1) from vanadate and tungstate-inhibited structures
Authors: Davies, D.R. / Interthal, H. / Champoux, J.J. / Hol, W.G.J.
#3: Journal: Structure / Year: 2002
Title: The crystal structure of human Tyrosyl-DNA Phosphodiesterase, Tdp1
Authors: Davies, D.R. / Interthal, H. / Champoux, J.J. / Hol, W.G.J.
History
DepositionNov 13, 2003Deposition site: RCSB / Processing site: RCSB
Revision 1.0Mar 2, 2004Provider: repository / Type: Initial release
Revision 1.1Apr 29, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Oct 27, 2021Group: Database references / Derived calculations
Category: database_2 / pdbx_struct_conn_angle ...database_2 / pdbx_struct_conn_angle / struct_conn / struct_ref_seq_dif / 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_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.ptnr1_label_seq_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.ptnr3_label_seq_id / _pdbx_struct_conn_angle.value / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_asym_id / _struct_conn.ptnr1_auth_comp_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_asym_id / _struct_conn.ptnr1_label_atom_id / _struct_conn.ptnr1_label_comp_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_asym_id / _struct_conn.ptnr2_auth_comp_id / _struct_conn.ptnr2_auth_seq_id / _struct_conn.ptnr2_label_asym_id / _struct_conn.ptnr2_label_atom_id / _struct_conn.ptnr2_label_comp_id / _struct_ref_seq_dif.details / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id
Revision 1.4Aug 23, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
D: 5'-D(*GP*TP*T)-3'
F: 5'-D(*GP*TP*T)-3'
A: Tyrosyl-DNA phosphodiesterase 1
B: Tyrosyl-DNA phosphodiesterase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)111,9869
Polymers111,2484
Non-polymers7395
Water4,089227
1
D: 5'-D(*GP*TP*T)-3'
A: Tyrosyl-DNA phosphodiesterase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)56,0945
Polymers55,6242
Non-polymers4703
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
F: 5'-D(*GP*TP*T)-3'
B: Tyrosyl-DNA phosphodiesterase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)55,8924
Polymers55,6242
Non-polymers2682
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)49.692, 104.750, 194.033
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121
DetailsThere are two biological assemblies per asymmetric unit: chains A and D, and chains B and F

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Components

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DNA chain / Protein , 2 types, 4 molecules DFAB

#1: DNA chain 5'-D(*GP*TP*T)-3'


Mass: 892.634 Da / Num. of mol.: 2 / Source method: obtained synthetically
#2: Protein Tyrosyl-DNA phosphodiesterase 1 / 3.1.4.- / Tyr-DNA phosphodiesterase 1 / TDP1


Mass: 54731.195 Da / Num. of mol.: 2 / Fragment: residues 149-608 / Mutation: N322D, T328M, L548F
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: TDP1 / Plasmid: pET15b / Species (production host): Escherichia coli / Production host: Escherichia coli BL21 (bacteria) / Strain (production host): BL21
References: UniProt: Q9NUW8, Hydrolases; Acting on ester bonds; Phosphoric-diester hydrolases

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Non-polymers , 4 types, 232 molecules

#3: Chemical ChemComp-VO4 / VANADATE ION


Mass: 114.939 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: VO4
#4: Chemical ChemComp-SPM / SPERMINE


Mass: 202.340 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C10H26N4
#5: Chemical ChemComp-OTS / 4-(2S-AMINO-1-HYDROXYETHYL)PHENOL / S-OCTOPAMINE


Mass: 153.178 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C8H11NO2
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 227 / Source method: isolated from a natural source / Formula: H2O

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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: 2.27 Å3/Da / Density % sol: 45.76 %
Crystal growTemperature: 298 K / Method: vapor diffusion, sitting drop / pH: 7.8
Details: PEG 3000, NaCl, HEPES, spermine, pH 7.8, VAPOR DIFFUSION, SITTING DROP, temperature 298K
Components of the solutions
IDNameCrystal-IDSol-ID
1PEG 300011
2NaCl11
3HEPES11
4spermine11
5H2O11
6PEG 300012
7NaCl12
8H2O12
Crystal grow
*PLUS
pH: 8.2 / Method: vapor diffusion, sitting drop
Components of the solutions
*PLUS
IDConc.Common nameCrystal-IDSol-IDChemical formulaDetails
16.5 mg/mlprotein1drop
2250 mM1dropNaCl
315 mMTris1droppH8.2
41 mMEDTA1drop
519-21 %PEG30001reservoir
6200 mM1reservoirNaCl
710 mMspermine1reservoir
8100 mMHEPES1reservoiror MOPS, pH7.8

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: ALS / Beamline: 8.2.2 / Wavelength: 0.9791 Å
DetectorType: ADSC QUANTUM 4 / Detector: CCD / Date: Feb 1, 2003
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9791 Å / Relative weight: 1
ReflectionResolution: 2.3→50 Å / Num. all: 46407 / Num. obs: 46407 / % possible obs: 99.1 % / Observed criterion σ(F): 0 / Observed criterion σ(I): -3 / Redundancy: 4.9 % / Rsym value: 0.118 / Net I/σ(I): 13.72
Reflection shellResolution: 2.3→2.36 Å / Mean I/σ(I) obs: 2.53 / Rsym value: 0.505 / % possible all: 50.5
Reflection
*PLUS
Rmerge(I) obs: 0.118
Reflection shell
*PLUS
% possible obs: 50.5 % / Rmerge(I) obs: 0.505

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Processing

Software
NameVersionClassification
REFMAC5.1.24refinement
HKL-2000data reduction
SCALEPACKdata scaling
AMoREphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB entry 1JY1

1jy1


Resolution: 2.3→50 Å / Cor.coef. Fo:Fc: 0.943 / Cor.coef. Fo:Fc free: 0.917 / SU B: 6.108 / SU ML: 0.149 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.309 / ESU R Free: 0.224 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.2347 2312 5.1 %RANDOM
Rwork0.18819 ---
all0.19052 45642 --
obs0.19052 43330 99.12 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: BABINET MODEL WITH MASK
Displacement parametersBiso mean: 27.645 Å2
Baniso -1Baniso -2Baniso -3
1--1.19 Å20 Å20 Å2
2--2.59 Å20 Å2
3----1.41 Å2
Refinement stepCycle: LAST / Resolution: 2.3→50 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms6820 80 38 227 7165
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0110.0217166
X-RAY DIFFRACTIONr_bond_other_d0.0030.0238
X-RAY DIFFRACTIONr_angle_refined_deg1.2411.9549748
X-RAY DIFFRACTIONr_angle_other_deg0.123.48714
X-RAY DIFFRACTIONr_dihedral_angle_1_deg6.2795847
X-RAY DIFFRACTIONr_chiral_restr0.0880.21029
X-RAY DIFFRACTIONr_gen_planes_refined0.0050.025409
X-RAY DIFFRACTIONr_nbd_refined0.2160.33182
X-RAY DIFFRACTIONr_nbd_other0.4280.353
X-RAY DIFFRACTIONr_nbtor_other0.2370.55
X-RAY DIFFRACTIONr_xyhbond_nbd_refined0.1860.5657
X-RAY DIFFRACTIONr_metal_ion_refined0.120.52
X-RAY DIFFRACTIONr_symmetry_vdw_refined0.2080.346
X-RAY DIFFRACTIONr_symmetry_hbond_refined0.1020.54
X-RAY DIFFRACTIONr_mcbond_it1.52334269
X-RAY DIFFRACTIONr_mcangle_it2.61646885
X-RAY DIFFRACTIONr_scbond_it2.71242897
X-RAY DIFFRACTIONr_scangle_it4.05362863
LS refinement shellResolution: 2.3→2.36 Å / Total num. of bins used: 20 /
RfactorNum. reflection
Rfree0.289 180
Rwork0.223 3052
Refinement
*PLUS
Highest resolution: 2.3 Å / Lowest resolution: 50 Å / Rfactor Rfree: 0.239 / Rfactor Rwork: 0.199
Solvent computation
*PLUS
Displacement parameters
*PLUS
Refine LS restraints
*PLUS
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONr_bond_d0.011
X-RAY DIFFRACTIONr_angle_d
X-RAY DIFFRACTIONr_angle_deg1.241

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