3im2

Structure of the C-terminal Sec63 unit of yeast Brr2, P41212 Form

Method: X-RAY DIFFRACTION Dmax: 72.2 Å Quality: EXCELLENT

1. Protein Identity and Related Structures Protein Identity & Related Structures

Pre-mRNA-splicing helicase BRR2

Saccharomyces cerevisiae

UniProt P32639

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1839–2163 Fragment:Sec63 unit (UNP residues 1839-2163) PG4 TETRAETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;293 K;100mM sodium cacodylate, pH 6.0, 100mM Li2SO4, 15 % PEG 4000, VAPOR DIFFUSION, HANGING DROP, temperature 293K Resolution 1.99 Å R-free 0.237

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

17 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BRR2_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–328; UniProt 1839–2163

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 3im2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3im2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3im2
Deposition date deposition_date2009-08-09
Structure title titleStructure of the C-terminal Sec63 unit of yeast Brr2, P41212 Form
Keywords keywords;ATPase, RNA helicase, RNPase, RNA unwindase, molecular modeling, pre-mRNA splicing, spliceosome catalytic activation, U5-200K protein/Brr2, ATP-binding, Helicase, Hydrolase, mRNA processing, mRNA splicing, Nucleotide-binding, Nucleus, Phosphoprotein, Spliceosome ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier22.69
Radius of gyration Rg (electron density) rg_electron21.48
Forward intensity I(0) i021482200.00
Molecular weight molecular_weight36500.0 kDa
Excluded volume excluded_volume46330 ų
Envelope volume envelope_volume56306 ų
Hydration-shell volume shell_volume22131 ų
Envelope diameter envelope_diameter74.8
Shell Rg shell_rg27.91
Envelope Rg envelope_rg21.81
Shape Rg shape_rg21.46
Total Rg total_rg22.44
Total atoms total_atoms2573
Residues n_residues320
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax72.2
Rg (real space) rg_real22.63
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real2.1480e+07
I(0) uncertainty (real space) i0_real_error2.9090e+05
Rg (reciprocal space) rg_reciprocal22.65
I(0) (reciprocal space) i0_reciprocal21480000.0000
Solution quality estimate total_estimate0.9057
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.3
Skewness Skewness skewness0.235
Kurtosis Kurtosis kurtosis-0.502
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7635000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.924; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.998

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id3im2A01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3380 — Sec63 N-terminal domain-like fold
Homologous superfamily homologous superfamily10 — Sec63 N-terminal domain-like domain

8. Citations (1)

9. Files and Curves (10)