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- PDB-2x1b: Structure of RNA15 RRM -

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Basic information

Entry
Database: PDB / ID: 2x1b
TitleStructure of RNA15 RRM
ComponentsMRNA 3'-END-PROCESSING PROTEIN RNA15
KeywordsTRANSCRIPTION / NUCLEUS / RNA-BINDING / MRNA PROCESSING
Function / homology
Function and homology information


mRNA cleavage stimulating factor complex / mRNA cleavage factor complex / mRNA cleavage and polyadenylation specificity factor complex / mRNA 3'-end processing / mRNA processing / molecular adaptor activity / mRNA binding
Similarity search - Function
Transcription termination and cleavage factor, C-terminal domain / Transcription termination and cleavage factor, C-terminal domain superfamily / Transcription termination and cleavage factor C-terminal / RRM (RNA recognition motif) domain / RNA recognition motif / RNA recognition motif / Eukaryotic RNA Recognition Motif (RRM) profile. / RNA recognition motif domain / RNA-binding domain superfamily / Nucleotide-binding alpha-beta plait domain superfamily ...Transcription termination and cleavage factor, C-terminal domain / Transcription termination and cleavage factor, C-terminal domain superfamily / Transcription termination and cleavage factor C-terminal / RRM (RNA recognition motif) domain / RNA recognition motif / RNA recognition motif / Eukaryotic RNA Recognition Motif (RRM) profile. / RNA recognition motif domain / RNA-binding domain superfamily / Nucleotide-binding alpha-beta plait domain superfamily / Alpha-Beta Plaits / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
PHOSPHATE ION / mRNA 3'-end-processing protein RNA15
Similarity search - Component
Biological speciesSACCHAROMYCES CEREVISIAE (brewer's yeast)
MethodX-RAY DIFFRACTION / OTHER / Resolution: 1.8 Å
AuthorsPancevac, C. / Goldstone, D.C. / Ramos, A. / Taylor, I.A.
CitationJournal: Nucleic Acids Res. / Year: 2010
Title: Structure of the RNA15 Rrm-RNA Complex Reveals the Molecular Basis of Gu Specificity in Transcriptional 3-End Processing Factors.
Authors: Pancevac, C. / Goldstone, D.C. / Ramos, A. / Taylor, I.A.
History
DepositionJan 6, 2010Deposition site: PDBE / Processing site: PDBE
Revision 1.0Feb 2, 2010Provider: repository / Type: Initial release
Revision 1.1May 8, 2011Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3May 8, 2024Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Other
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_database_status / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_database_status.status_code_sf / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: MRNA 3'-END-PROCESSING PROTEIN RNA15
hetero molecules


Theoretical massNumber of molelcules
Total (without water)10,8962
Polymers10,8011
Non-polymers951
Water2,648147
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)26.990, 36.795, 92.838
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

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Components

#1: Protein MRNA 3'-END-PROCESSING PROTEIN RNA15 / RNA15 RRM


Mass: 10800.948 Da / Num. of mol.: 1 / Fragment: RNA RECOGNITION MODULE, RESIDUES 16-111
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) SACCHAROMYCES CEREVISIAE (brewer's yeast)
Production host: ESCHERICHIA COLI (E. coli) / References: UniProt: P25299
#2: Chemical ChemComp-PO4 / PHOSPHATE ION


Mass: 94.971 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: PO4
#3: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 147 / 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: 2.13 Å3/Da / Density % sol: 42.36 % / Description: NONE

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: ROTATING ANODE / Wavelength: 1.5418
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.5418 Å / Relative weight: 1
ReflectionResolution: 1.8→20 Å / Num. obs: 9150 / % possible obs: 99.7 % / Observed criterion σ(I): 2 / Redundancy: 7.4 % / Biso Wilson estimate: 18.1 Å2 / Rmerge(I) obs: 0.06 / Net I/σ(I): 31.6

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Processing

SoftwareName: REFMAC / Version: 5.5.0088 / Classification: refinement
RefinementMethod to determine structure: OTHER / Resolution: 1.8→46.42 Å / Cor.coef. Fo:Fc: 0.951 / Cor.coef. Fo:Fc free: 0.935 / SU B: 2.295 / SU ML: 0.072 / Cross valid method: THROUGHOUT / ESU R: 0.132 / ESU R Free: 0.128 / Stereochemistry target values: MAXIMUM LIKELIHOOD
Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. U VALUES REFINED INDIVIDUALLY.
RfactorNum. reflection% reflectionSelection details
Rfree0.22565 431 4.8 %RANDOM
Rwork0.18301 ---
obs0.18499 8628 99.64 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: MASK
Displacement parametersBiso mean: 14.43 Å2
Baniso -1Baniso -2Baniso -3
1--0.07 Å20 Å20 Å2
2--0.09 Å20 Å2
3----0.02 Å2
Refinement stepCycle: LAST / Resolution: 1.8→46.42 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms670 0 5 147 822
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.010.022693
X-RAY DIFFRACTIONr_bond_other_d0.0140.02478
X-RAY DIFFRACTIONr_angle_refined_deg1.161.981936
X-RAY DIFFRACTIONr_angle_other_deg0.90531162
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.289588
X-RAY DIFFRACTIONr_dihedral_angle_2_deg36.03724.24233
X-RAY DIFFRACTIONr_dihedral_angle_3_deg10.73315117
X-RAY DIFFRACTIONr_dihedral_angle_4_deg9.455155
X-RAY DIFFRACTIONr_chiral_restr0.0760.299
X-RAY DIFFRACTIONr_gen_planes_refined0.0040.021782
X-RAY DIFFRACTIONr_gen_planes_other0.0010.02143
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_it0.6861.5432
X-RAY DIFFRACTIONr_mcbond_other0.1541.5179
X-RAY DIFFRACTIONr_mcangle_it1.3242693
X-RAY DIFFRACTIONr_mcangle_other
X-RAY DIFFRACTIONr_scbond_it2.3193261
X-RAY DIFFRACTIONr_scbond_other
X-RAY DIFFRACTIONr_scangle_it4.0414.5242
X-RAY DIFFRACTIONr_scangle_other
X-RAY DIFFRACTIONr_long_range_B_refined
X-RAY DIFFRACTIONr_long_range_B_other
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 1.8→1.847 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.243 31 -
Rwork0.363 597 -
obs--97.06 %

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