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- PDB-3htx: Crystal structure of small RNA methyltransferase HEN1 -

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Basic information

Entry
Database: PDB / ID: 3htx
TitleCrystal structure of small RNA methyltransferase HEN1
Components
  • 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'
  • 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'
  • HEN1
KeywordsTRANSFERASE/RNA / HEN1 / small RNA methyltransferase / protein-RNA complex / SAM binding protein / TRANSFERASE-RNA COMPLEX
Function / homology
Function and homology information


: / : / specification of floral organ identity / leaf proximal/distal pattern formation / RNAi-mediated antiviral immune response / regulation of flower development / leaf vascular tissue pattern formation / miRNA-mediated gene silencing by mRNA destabilization / piRNA processing / RNA methyltransferase activity ...: / : / specification of floral organ identity / leaf proximal/distal pattern formation / RNAi-mediated antiviral immune response / regulation of flower development / leaf vascular tissue pattern formation / miRNA-mediated gene silencing by mRNA destabilization / piRNA processing / RNA methyltransferase activity / miRNA processing / siRNA processing / O-methyltransferase activity / RNA binding / nucleus / metal ion binding / cytoplasm
Similarity search - Function
Small RNA 2'-O-methyltransferase Hen1, La-motif C-terminal domain / HEN1, double-stranded RNA binding domain 2 / Double-stranded RNA binding domain 2 / Hen1 La-motif C-terminal domain / 3'-RNA ribose 2'-O-methyltransferase, Hen1 / La-type HTH domain / La-type HTH domain profile. / Methyltransferase domain / Methyltransferase domain / Double Stranded RNA Binding Domain - #20 ...Small RNA 2'-O-methyltransferase Hen1, La-motif C-terminal domain / HEN1, double-stranded RNA binding domain 2 / Double-stranded RNA binding domain 2 / Hen1 La-motif C-terminal domain / 3'-RNA ribose 2'-O-methyltransferase, Hen1 / La-type HTH domain / La-type HTH domain profile. / Methyltransferase domain / Methyltransferase domain / Double Stranded RNA Binding Domain - #20 / Double Stranded RNA Binding Domain / Vaccinia Virus protein VP39 / S-adenosyl-L-methionine-dependent methyltransferase superfamily / Rossmann fold / 2-Layer Sandwich / 3-Layer(aba) Sandwich / Alpha Beta
Similarity search - Domain/homology
S-ADENOSYL-L-HOMOCYSTEINE / RNA / RNA (> 10) / Small RNA 2'-O-methyltransferase / Small RNA 2'-O-methyltransferase
Similarity search - Component
Biological speciesArabidopsis thaliana (thale cress)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MAD / Resolution: 3.1 Å
AuthorsHuang, Y. / Ji, L.-J. / Huang, Q.-C. / Vassylyev, D.G. / Chen, X.-M. / Ma, J.-B.
CitationJournal: Nature / Year: 2009
Title: Structural insights into mechanisms of the small RNA methyltransferase HEN1.
Authors: Huang, Y. / Ji, L. / Huang, Q. / Vassylyev, D.G. / Chen, X. / Ma, J.B.
History
DepositionJun 12, 2009Deposition site: RCSB / Processing site: RCSB
Revision 1.0Sep 29, 2009Provider: repository / Type: Initial release
Revision 1.1Jul 13, 2011Group: Version format compliance
Revision 1.2Oct 13, 2021Group: Database references / Derived calculations
Category: database_2 / struct_conn ...database_2 / 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 / _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_conn.ptnr2_label_seq_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 1.3Feb 21, 2024Group: Data collection / Category: chem_comp_atom / chem_comp_bond

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: HEN1
B: 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'
C: 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'
D: HEN1
E: 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'
F: 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'
hetero molecules


Theoretical massNumber of molelcules
Total (without water)240,02510
Polymers239,2086
Non-polymers8174
Water66737
1
A: HEN1
B: 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'
C: 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'
hetero molecules


Theoretical massNumber of molelcules
Total (without water)120,0135
Polymers119,6043
Non-polymers4092
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area7380 Å2
ΔGint-51.3 kcal/mol
Surface area43330 Å2
MethodPISA
2
D: HEN1
E: 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'
F: 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'
hetero molecules


Theoretical massNumber of molelcules
Total (without water)120,0135
Polymers119,6043
Non-polymers4092
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area7160 Å2
ΔGint-54.5 kcal/mol
Surface area44090 Å2
MethodPISA
Unit cell
Length a, b, c (Å)96.995, 124.347, 101.376
Angle α, β, γ (deg.)90.000, 93.470, 90.000
Int Tables number4
Space group name H-MP1211

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Components

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Protein , 1 types, 2 molecules AD

#1: Protein HEN1


Mass: 105542.500 Da / Num. of mol.: 2 / Mutation: L604P, R640K
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Arabidopsis thaliana (thale cress) / Gene: HEN1 / Plasmid: pET28a / Production host: Escherichia coli (E. coli) / Strain (production host): BL21(DE3) / References: UniProt: Q945R3, UniProt: Q9C5Q8*PLUS

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RNA chain , 2 types, 4 molecules BECF

#2: RNA chain 5'-R(*GP*AP*UP*UP*UP*CP*UP*CP*UP*CP*UP*GP*CP*AP*AP*GP*CP*GP*AP*AP*AP*G)-3'


Mass: 7019.211 Da / Num. of mol.: 2 / Source method: obtained synthetically
#3: RNA chain 5'-R(P*UP*UP*CP*GP*CP*UP*UP*GP*CP*AP*GP*AP*GP*AP*GP*AP*AP*AP*UP*CP*AP*C)-3'


Mass: 7042.251 Da / Num. of mol.: 2 / Source method: obtained synthetically

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Non-polymers , 3 types, 41 molecules

#4: Chemical ChemComp-MG / MAGNESIUM ION


Mass: 24.305 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Mg
#5: Chemical ChemComp-SAH / S-ADENOSYL-L-HOMOCYSTEINE


Type: L-peptide linking / Mass: 384.411 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C14H20N6O5S
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 37 / 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: 2.55 Å3/Da / Density % sol: 51.78 %
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop / pH: 4.8
Details: 0.1 M Phosphate-citrate pH 4.8, 15% PEG 3350, 0.2 M NaCl, 0.01M NaBr, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Components of the solutions
IDNameCrystal-IDSol-ID
1Phosphate-citrate11
2PEG 335011
3NaCl11
4NaBr11
5Phosphate-citrate12
6PEG 335012
7NaCl12
8NaBr12

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Data collection

Diffraction
IDMean temperature (K)Crystal-ID
11001
21001
Diffraction source
SourceSiteBeamlineIDWavelength (Å)
SYNCHROTRONAPS 19-BM10.9793
SYNCHROTRONAPS 23-ID-B20.97950, 0.97967, 0.94950
Detector
TypeIDDetectorDate
MARMOSAIC 300 mm CCD1CCDNov 17, 2008
ADSC QUANTUM 210r2CCDJun 6, 2008
Radiation
IDProtocolMonochromatic (M) / Laue (L)Scattering typeWavelength-ID
1SINGLE WAVELENGTHMx-ray1
2MADMx-ray1
Radiation wavelength
IDWavelength (Å)Relative weight
10.97931
20.97951
30.979671
40.94951
ReflectionResolution: 3.1→20 Å / Num. all: 40959 / Num. obs: 40959 / % possible obs: 92.8 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 3 % / Rmerge(I) obs: 0.097 / Net I/σ(I): 8.7
Reflection shellResolution: 3.1→3.21 Å / Redundancy: 2 % / Rmerge(I) obs: 0.489 / Mean I/σ(I) obs: 1.8 / Num. unique all: 3559 / % possible all: 81.8

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Processing

Software
NameVersionClassificationNB
CNSrefinement
PDB_EXTRACT3.005data extraction
ADSCQuantumdata collection
HKL-2000data reduction
HKL-2000data scaling
SOLVEphasing
RefinementMethod to determine structure: MAD / Resolution: 3.1→20 Å / Occupancy max: 1 / Occupancy min: 1
RfactorNum. reflection% reflection
Rfree0.288 2023 4.6 %
Rwork0.26 --
obs0.26 40394 92.8 %
Solvent computationBsol: 15.34 Å2
Displacement parametersBiso max: 199.86 Å2 / Biso mean: 106.353 Å2 / Biso min: 15.66 Å2
Baniso -1Baniso -2Baniso -3
1--11.426 Å20 Å23.371 Å2
2--4.743 Å20 Å2
3---6.683 Å2
Refinement stepCycle: LAST / Resolution: 3.1→20 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms12310 1868 54 37 14269
Refine LS restraints
Refine-IDTypeDev idealDev ideal target
X-RAY DIFFRACTIONc_mcbond_it1.6981.5
X-RAY DIFFRACTIONc_scbond_it2.8382
X-RAY DIFFRACTIONc_mcangle_it3.1262
X-RAY DIFFRACTIONc_scangle_it3.6612.5
Xplor file
Refine-IDSerial noParam file
X-RAY DIFFRACTION1CNS_TOPPAR:protein_rep.param
X-RAY DIFFRACTION2CNS_TOPPAR:dna-rna_rep.param
X-RAY DIFFRACTION3sah_par.txt
X-RAY DIFFRACTION4CNS_TOPPAR:ion.param
X-RAY DIFFRACTION5CNS_TOPPAR:water_rep.param

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