4qqb

Structural basis for the assembly of the SXL-UNR translation regulatory complex

Method: X-RAY DIFFRACTION Dmax: 100.9 Å Quality: GOOD

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

Protein sex-lethal

Drosophila melanogaster

UniProt P19339

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–RNA Heteromer Protein × 2 RNA 1 PDB declaration: trimeric(3) Consistent with all polymer counts Chain A; UniProt 122–294 Fragment:RRM1-RRM2, UNP residues 122-294 msl2 mRNA × 1 Upstream of N-ras, isoform A × 1 (Q9VSK3) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;0.1 M LiSO4, PEG3350 1-5 %, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 2.80 Å R-free 0.236
2 Protein–RNA Heteromer Protein × 2 RNA 1 PDB declaration: trimeric(3) Consistent with all polymer counts Chain B; UniProt 122–294 Fragment:RRM1-RRM2, UNP residues 122-294 msl2 mRNA × 1 Upstream of N-ras, isoform A × 1 (Q9VSK3) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;0.1 M LiSO4, PEG3350 1-5 %, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 2.80 Å R-free 0.236

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.

4 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SXL_DROME
Isoform
PDB entities 2
Chains and sequence ranges Author chain A; PDBConstruct 4–176; UniProt 122–294 Author chain B; PDBConstruct 4–176; UniProt 122–294

Upstream of N-ras, isoform A

Drosophila melanogaster

UniProt Q9VSK3

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–RNA Heteromer Protein × 2 RNA 1 PDB declaration: trimeric(3) Consistent with all polymer counts Chain X; UniProt 185–252 Fragment:CSD1, UNP residues 185-252 msl2 mRNA × 1 Protein sex-lethal × 1 (P19339) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;0.1 M LiSO4, PEG3350 1-5 %, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 2.80 Å R-free 0.236
2 Protein–RNA Heteromer Protein × 2 RNA 1 PDB declaration: trimeric(3) Consistent with all polymer counts Chain Y; UniProt 185–252 Fragment:CSD1, UNP residues 185-252 msl2 mRNA × 1 Protein sex-lethal × 1 (P19339) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;0.1 M LiSO4, PEG3350 1-5 %, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 2.80 Å R-free 0.236

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.

6 other PDB entries and 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q9VSK3_DROME
Isoform
PDB entities 3
Chains and sequence ranges Author chain X; PDBConstruct 5–72; UniProt 185–252 Author chain Y; PDBConstruct 5–72; UniProt 185–252

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 4qqb

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4qqb
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4qqb
Deposition date deposition_date2014-06-27
Structure title titleStructural basis for the assembly of the SXL-UNR translation regulatory complex
Keywords keywords;RNA binding domains, RNA recognition motif, RRM, cold shock domain, CSD, RNA binding, translation regulation, dosage compensation, TRANSCRIPTION-RNA complex, TRANLATION-RNA complex ;; TRANLATION/RNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.01
Radius of gyration Rg (electron density) rg_electron29.93
Forward intensity I(0) i086967100.00
Molecular weight molecular_weight65459.0 kDa
Excluded volume excluded_volume78453 ų
Envelope volume envelope_volume106060 ų
Hydration-shell volume shell_volume30637 ų
Envelope diameter envelope_diameter110.3
Shell Rg shell_rg35.28
Envelope Rg envelope_rg29.97
Shape Rg shape_rg29.94
Total Rg total_rg30.36
Total atoms total_atoms4556
Residues n_residues516
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 dmax100.9
Rg (real space) rg_real30.10
Rg uncertainty (real space) rg_real_error1.02
I(0) (real space) i0_real8.6970e+07
I(0) uncertainty (real space) i0_real_error1.4920e+06
Rg (reciprocal space) rg_reciprocal30.06
I(0) (reciprocal space) i0_reciprocal86960000.0000
Solution quality estimate total_estimate0.8054
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary38.1
Skewness Skewness skewness0.396
Kurtosis Kurtosis kurtosis-0.312
Angular range angular_range— – 0.2650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha19730000.0000
Real-space data points n_real_points54
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.848; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.923; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 6 domains

CATH v4.4 (6 domains)

Domain ID domain_id4qqbA01
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain
Domain ID domain_id4qqbA02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain
Domain ID domain_id4qqbB01
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain
Domain ID domain_id4qqbB02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain
Domain ID domain_id4qqbX01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins
Domain ID domain_id4qqbY01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins

8. Citations (1)

9. Files and Curves (10)