2kn4

The structure of the RRM domain of SC35

Method: SOLUTION NMR Dmax: 103.5 Å Quality: REASONABLE

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

Immunoglobulin G-binding protein G,Serine/arginine-rich splicing factor 2

Homo sapiens

UniProt P19909

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 304–357 Fragment:UNP residues 304-357 from P19909, UNP residues 9-101 from Q01130 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.8;305 K;Ionic strength (raw mmCIF value) 100;Pressure ambient NMR sample composition:0.5 mM [U-100% 13C; U-100% 15N] SC35-1, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.5 mM [U-100% 13C; U-100% 15N] SC35-2, 100% D2O | 100% D2O NMR sample composition:0.5 mM [U-100% 15N] SC35-3, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.5 mM SC35-4, 100% D2O | 100% D2O Resolution not provided

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.

76 other PDB entries and 116 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPG2_STRSG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–56; UniProt 304–357

Immunoglobulin G-binding protein G,Serine/arginine-rich splicing factor 2

Homo sapiens

UniProt Q01130

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 9–101 Fragment:UNP residues 304-357 from P19909, UNP residues 9-101 from Q01130 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.8;305 K;Ionic strength (raw mmCIF value) 100;Pressure ambient NMR sample composition:0.5 mM [U-100% 13C; U-100% 15N] SC35-1, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.5 mM [U-100% 13C; U-100% 15N] SC35-2, 100% D2O | 100% D2O NMR sample composition:0.5 mM [U-100% 15N] SC35-3, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.5 mM SC35-4, 100% D2O | 100% D2O Resolution not provided

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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SRSF2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 66–158; UniProt 9–101

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 2kn4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2kn4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2kn4
Deposition date deposition_date2009-08-14
Structure title titleThe structure of the RRM domain of SC35
Keywords keywords;RRM domain, Cell wall, IgG-binding protein, Peptidoglycan-anchor, Secreted, mRNA processing, mRNA splicing, Nucleus, Phosphoprotein, RNA-binding, RNA BINDING PROTEIN ;; RNA BINDING PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier25.63
Radius of gyration Rg (electron density) rg_electron26.01
Forward intensity I(0) i02112180000.00
Molecular weight molecular_weight361940.0 kDa
Excluded volume excluded_volume442530 ų
Envelope volume envelope_volume205060 ų
Hydration-shell volume shell_volume48700 ų
Envelope diameter envelope_diameter118.7
Shell Rg shell_rg41.10
Envelope Rg envelope_rg36.51
Shape Rg shape_rg26.00
Total Rg total_rg26.46
Total atoms total_atoms49620
Residues n_residues3160
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 dmax103.5
Rg (real space) rg_real26.06
Rg uncertainty (real space) rg_real_error1.24
I(0) (real space) i0_real2.1120e+09
I(0) uncertainty (real space) i0_real_error3.5670e+07
Rg (reciprocal space) rg_reciprocal25.93
I(0) (reciprocal space) i0_reciprocal2112000000.0000
Solution quality estimate total_estimate0.6846
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.0
Skewness Skewness skewness0.682
Kurtosis Kurtosis kurtosis-0.086
Angular range angular_range— – 0.3100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3917000.0000
Real-space data points n_real_points63
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.268; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.102; Smooth: 0.990

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id2kn4A01
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily10
Domain ID domain_id2kn4A02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain

8. Citations (1)

9. Files and Curves (10)