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- PDB-7yc7: Dark, fully reduced structure of the MmCPDII-DNA complex as produ... -

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Basic information

Entry
Database: PDB / ID: 7yc7
TitleDark, fully reduced structure of the MmCPDII-DNA complex as produced at SwissFEL
Components
  • CPD photolesion containing DNA
  • Deoxyribodipyrimidine photo-lyase
  • complementary oligonucleotide to the CPD containing DNA
KeywordsDNA BINDING PROTEIN / Flavoprotein / photolyase / light driven electron transfer / DNA repair / time-resolved serial crystallography.
Function / homology
Function and homology information


deoxyribodipyrimidine photo-lyase / deoxyribodipyrimidine photo-lyase activity / DNA repair / DNA binding
Similarity search - Function
DNA photolyase class 2 / : / DNA photolyase, N-terminal / Cryptochrome/photolyase, N-terminal domain superfamily / DNA photolyase / Photolyase/cryptochrome alpha/beta domain profile. / Cryptochrome/DNA photolyase, FAD-binding domain-like superfamily / Rossmann-like alpha/beta/alpha sandwich fold
Similarity search - Domain/homology
FLAVIN-ADENINE DINUCLEOTIDE / DNA / DNA (> 10) / Deoxyribodipyrimidine photo-lyase
Similarity search - Component
Biological speciesMethanosarcina mazei (archaea)
synthetic construct (others)
MethodX-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 1.95 Å
AuthorsMaestre-Reyna, M. / Wang, P.-H. / Nango, E. / Hosokawa, Y. / Saft, M. / Furrer, A. / Yang, C.-H. / Ngura Putu, E.P.G. / Wu, W.-J. / Emmerich, H.-J. ...Maestre-Reyna, M. / Wang, P.-H. / Nango, E. / Hosokawa, Y. / Saft, M. / Furrer, A. / Yang, C.-H. / Ngura Putu, E.P.G. / Wu, W.-J. / Emmerich, H.-J. / Engilberge, S. / Caramello, N. / Wranik, M. / Glover, H.L. / Franz-Badur, S. / Wu, H.-Y. / Lee, C.-C. / Huang, W.-C. / Huang, K.-F. / Chang, Y.-K. / Liao, J.-H. / Weng, J.-H. / Gad, W. / Chang, C.-W. / Pang, A.H. / Gashi, D. / Beale, E. / Ozerov, D. / Milne, C. / Cirelli, C. / Bacellar, C. / Sugahara, M. / Owada, S. / Joti, Y. / Yamashita, A. / Tanaka, R. / Tanaka, T. / Luo, F.J. / Tono, K. / Kiontke, S. / Spadaccini, R. / Royant, A. / Yamamoto, J. / Iwata, S. / Standfuss, J. / Essen, L.-O. / Bessho, Y. / Tsai, M.-D.
Funding support Taiwan, Japan, 3items
OrganizationGrant numberCountry
Ministry of Science and Technology (MoST, Taiwan)AS-KPQ-105-TPP Taiwan
Ministry of Science and Technology (MoST, Taiwan)AS-KPQ-109-TPP2 Taiwan
Japan Society for the Promotion of Science (JSPS)16K01942 Japan
CitationJournal: Science / Year: 2023
Title: Visualizing the DNA repair process by a photolyase at atomic resolution.
Authors: Maestre-Reyna, M. / Wang, P.H. / Nango, E. / Hosokawa, Y. / Saft, M. / Furrer, A. / Yang, C.H. / Gusti Ngurah Putu, E.P. / Wu, W.J. / Emmerich, H.J. / Caramello, N. / Franz-Badur, S. / Yang, ...Authors: Maestre-Reyna, M. / Wang, P.H. / Nango, E. / Hosokawa, Y. / Saft, M. / Furrer, A. / Yang, C.H. / Gusti Ngurah Putu, E.P. / Wu, W.J. / Emmerich, H.J. / Caramello, N. / Franz-Badur, S. / Yang, C. / Engilberge, S. / Wranik, M. / Glover, H.L. / Weinert, T. / Wu, H.Y. / Lee, C.C. / Huang, W.C. / Huang, K.F. / Chang, Y.K. / Liao, J.H. / Weng, J.H. / Gad, W. / Chang, C.W. / Pang, A.H. / Yang, K.C. / Lin, W.T. / Chang, Y.C. / Gashi, D. / Beale, E. / Ozerov, D. / Nass, K. / Knopp, G. / Johnson, P.J.M. / Cirelli, C. / Milne, C. / Bacellar, C. / Sugahara, M. / Owada, S. / Joti, Y. / Yamashita, A. / Tanaka, R. / Tanaka, T. / Luo, F. / Tono, K. / Zarzycka, W. / Muller, P. / Alahmad, M.A. / Bezold, F. / Fuchs, V. / Gnau, P. / Kiontke, S. / Korf, L. / Reithofer, V. / Rosner, C.J. / Seiler, E.M. / Watad, M. / Werel, L. / Spadaccini, R. / Yamamoto, J. / Iwata, S. / Zhong, D. / Standfuss, J. / Royant, A. / Bessho, Y. / Essen, L.O. / Tsai, M.D.
History
DepositionJul 1, 2022Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Nov 22, 2023Provider: repository / Type: Initial release
Revision 1.1Dec 13, 2023Group: Database references / Category: citation / citation_author
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_PubMed / _citation.title
Revision 1.2Mar 13, 2024Group: Source and taxonomy / Category: entity_src_gen
Item: _entity_src_gen.gene_src_strain / _entity_src_gen.pdbx_gene_src_ncbi_taxonomy_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Deoxyribodipyrimidine photo-lyase
B: Deoxyribodipyrimidine photo-lyase
C: CPD photolesion containing DNA
D: complementary oligonucleotide to the CPD containing DNA
E: CPD photolesion containing DNA
F: complementary oligonucleotide to the CPD containing DNA
hetero molecules


Theoretical massNumber of molelcules
Total (without water)129,0399
Polymers127,3726
Non-polymers1,6673
Water5,260292
1
A: Deoxyribodipyrimidine photo-lyase
C: CPD photolesion containing DNA
D: complementary oligonucleotide to the CPD containing DNA
hetero molecules


Theoretical massNumber of molelcules
Total (without water)64,5685
Polymers63,6863
Non-polymers8822
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area5590 Å2
ΔGint-36 kcal/mol
Surface area21200 Å2
MethodPISA
2
B: Deoxyribodipyrimidine photo-lyase
E: CPD photolesion containing DNA
F: complementary oligonucleotide to the CPD containing DNA
hetero molecules


Theoretical massNumber of molelcules
Total (without water)64,4724
Polymers63,6863
Non-polymers7861
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area5520 Å2
ΔGint-17 kcal/mol
Surface area19880 Å2
MethodPISA
Unit cell
Length a, b, c (Å)72.440, 115.920, 169.230
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

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Components

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Protein , 1 types, 2 molecules AB

#1: Protein Deoxyribodipyrimidine photo-lyase / DNA photolyase


Mass: 55123.480 Da / Num. of mol.: 2 / Mutation: M377T
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Methanosarcina mazei (archaea)
Strain: (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88)
Gene: DU34_19720, DU35_15210, DU36_16165, DU37_08235, DU38_17340, DU39_00605, DU41_17975, DU42_05505, DU44_19145, DU46_16260, DU48_13210, DU49_01325, DU51_15440, DU57_04540, DU59_03190, DU60_01690, ...Gene: DU34_19720, DU35_15210, DU36_16165, DU37_08235, DU38_17340, DU39_00605, DU41_17975, DU42_05505, DU44_19145, DU46_16260, DU48_13210, DU49_01325, DU51_15440, DU57_04540, DU59_03190, DU60_01690, DU61_08490, DU62_04430, DU63_10745, DU65_18915, DU69_04700, DU71_05355, DU72_08110, DU74_09110, FQU78_02295
Production host: Escherichia coli BL21(DE3) (bacteria)
References: UniProt: A0A0F8I5V2, deoxyribodipyrimidine photo-lyase

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DNA chain , 2 types, 4 molecules CEDF

#2: DNA chain CPD photolesion containing DNA


Mass: 4256.768 Da / Num. of mol.: 2 / Source method: obtained synthetically / Details: TTD corresponds to a cyclobutane pyrimidine dimer / Source: (synth.) synthetic construct (others)
#3: DNA chain complementary oligonucleotide to the CPD containing DNA


Mass: 4305.805 Da / Num. of mol.: 2 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others)

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Non-polymers , 3 types, 295 molecules

#4: Chemical ChemComp-FAD / FLAVIN-ADENINE DINUCLEOTIDE


Mass: 785.550 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C27H33N9O15P2 / Feature type: SUBJECT OF INVESTIGATION / Comment: FAD*YM
#5: Chemical ChemComp-SO4 / SULFATE ION


Mass: 96.063 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: SO4
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 292 / Source method: isolated from a natural source / Formula: H2O

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Details

Has ligand of interestY

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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: 3.01 Å3/Da / Density % sol: 59.19 %
Crystal growTemperature: 296 K / Method: batch mode / pH: 4.6
Details: 100 mM Sodium Acetate pH 4.6 250 mM ammonium sulfate 4% PEG4000 (w/v) 50 mM DTT

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Data collection

DiffractionMean temperature: 298 K / Serial crystal experiment: Y
Diffraction sourceSource: FREE ELECTRON LASER / Site: SwissFEL ARAMIS / Beamline: ESA / Wavelength: 1.0875 Å
DetectorType: PSI JUNGFRAU 16M / Detector: PIXEL / Date: Sep 20, 2021
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.0875 Å / Relative weight: 1
ReflectionResolution: 1.93→17.08 Å / Num. obs: 107711 / % possible obs: 99.99 % / Redundancy: 2102.1 % / CC1/2: 0.997 / Net I/σ(I): 13.28
Reflection shellResolution: 1.93→1.95 Å / Redundancy: 441.2 % / Mean I/σ(I) obs: 1.84 / Num. unique obs: 5332 / CC1/2: 0.503 / % possible all: 100
Serial crystallography measurementXFEL pulse repetition rate: 100 Hz
Serial crystallography sample deliveryMethod: injection
Serial crystallography sample delivery injectionCarrier solvent: Grease matrix / Description: SwissFEL injector / Filter size: 20 µm / Flow rate: 4.2 µL/min / Injector diameter: 75 µm / Injector temperature: 298 K
Serial crystallography data reductionFrames indexed: 257381

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Processing

Software
NameVersionClassification
PHENIX(1.20.1_4487: ???)refinement
CrystFELdata reduction
pointlessdata scaling
REFMACphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 7YE0

7ye0


Resolution: 1.95→17.08 Å / SU ML: 0.17 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 16.63 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.175 5118 4.91 %
Rwork0.1541 --
obs0.1551 104265 100 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Refinement stepCycle: LAST / Resolution: 1.95→17.08 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms7044 1021 111 292 8468
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0168592
X-RAY DIFFRACTIONf_angle_d1.43811909
X-RAY DIFFRACTIONf_dihedral_angle_d19.8923183
X-RAY DIFFRACTIONf_chiral_restr0.0921258
X-RAY DIFFRACTIONf_plane_restr0.0121357
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.95-1.970.28711590.27133280X-RAY DIFFRACTION100
1.97-20.27521660.25423275X-RAY DIFFRACTION100
2-2.020.25181480.23933276X-RAY DIFFRACTION100
2.02-2.050.23031570.22913276X-RAY DIFFRACTION100
2.05-2.070.26942070.22533287X-RAY DIFFRACTION100
2.07-2.10.23571570.20853216X-RAY DIFFRACTION100
2.1-2.130.22191680.20233284X-RAY DIFFRACTION100
2.13-2.160.21391850.18883256X-RAY DIFFRACTION100
2.16-2.20.21141810.18853267X-RAY DIFFRACTION100
2.2-2.230.20451520.17843274X-RAY DIFFRACTION100
2.23-2.270.20261750.17793282X-RAY DIFFRACTION100
2.27-2.310.19171840.17113263X-RAY DIFFRACTION100
2.31-2.360.18322000.16723269X-RAY DIFFRACTION100
2.36-2.40.20421780.16593243X-RAY DIFFRACTION100
2.4-2.460.16991740.15993272X-RAY DIFFRACTION100
2.46-2.510.20191490.1623330X-RAY DIFFRACTION100
2.51-2.580.19131810.16453269X-RAY DIFFRACTION100
2.58-2.640.19411770.16563288X-RAY DIFFRACTION100
2.64-2.720.19131640.16373288X-RAY DIFFRACTION100
2.72-2.810.20011710.1713311X-RAY DIFFRACTION100
2.81-2.910.17031720.16513322X-RAY DIFFRACTION100
2.91-3.030.18681520.16463329X-RAY DIFFRACTION100
3.03-3.160.19121860.16053280X-RAY DIFFRACTION100
3.16-3.330.19831660.1553332X-RAY DIFFRACTION100
3.33-3.530.17421450.14463351X-RAY DIFFRACTION100
3.53-3.80.15291770.13113338X-RAY DIFFRACTION100
3.8-4.180.12091430.11933383X-RAY DIFFRACTION100
4.18-4.780.14591950.1243337X-RAY DIFFRACTION100
4.78-5.970.16861750.14243429X-RAY DIFFRACTION100
5.97-17.080.161740.15993540X-RAY DIFFRACTION100
Refinement TLS params.Method: refined / Origin x: -22.2966 Å / Origin y: -0.7825 Å / Origin z: -14.9096 Å
111213212223313233
T0.2445 Å20.012 Å20.0045 Å2-0.3135 Å20.0237 Å2--0.2541 Å2
L0.6184 °20.4808 °20.0519 °2-1.5789 °20.2262 °2--0.5882 °2
S-0.0712 Å °0.1007 Å °0.0324 Å °-0.1672 Å °0.1029 Å °0.0071 Å °0.082 Å °0.0472 Å °-0.0296 Å °
Refinement TLS groupSelection details: all

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