2c23

14-3-3 Protein Beta (Human) in complex with exoenzyme S peptide

Method: X-RAY DIFFRACTION Dmax: 65.7 Å Quality: REASONABLE

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

14-3-3 BETA/ALPHA

HOMO SAPIENS

UniProt P31946

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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–238 Not recorded EXOENZYME S PEPTIDE × 2 (Q51451) X-RAY DIFFRACTION X-ray crystallization conditions:pH 8;0.05M MGCL2,0.1M HEPES PH7.5, 30% PEG MME 550, pH 8.00 Resolution 2.65 Å R-free 0.286

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.

16 other PDB entries and 24 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name 1433B_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–239; UniProt 1–238

EXOENZYME S PEPTIDE

OrganismNot specified

UniProt Q51451

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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain P; UniProt 421–431 Fragment:14-3-3 BINDING REGION, RESIDUES 421-431 14-3-3 BETA/ALPHA × 2 (P31946) X-RAY DIFFRACTION X-ray crystallization conditions:pH 8;0.05M MGCL2,0.1M HEPES PH7.5, 30% PEG MME 550, pH 8.00 Resolution 2.65 Å R-free 0.286

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 Q51451_PSEAE
Isoform
PDB entities 2
Chains and sequence ranges Author chain P; PDBConstruct 1–11; UniProt 421–431

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 2c23

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2c23
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2c23
Deposition date deposition_date2005-09-26
Structure title title14-3-3 Protein Beta (Human) in complex with exoenzyme S peptide
Keywords keywords;SIGNALING PROTEIN, 14-3-3, YWHAB, EXOS, EXOENZYME S, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, ACETYLATION, ALTERNATIVE INITIATION, PHOSPHORYLATION, CELL REGULATOR PROTEIN ;; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.31
Radius of gyration Rg (electron density) rg_electron18.22
Forward intensity I(0) i012530200.00
Molecular weight molecular_weight26167.0 kDa
Excluded volume excluded_volume32616 ų
Envelope volume envelope_volume37669 ų
Hydration-shell volume shell_volume17554 ų
Envelope diameter envelope_diameter67.8
Shell Rg shell_rg24.13
Envelope Rg envelope_rg18.62
Shape Rg shape_rg18.20
Total Rg total_rg19.17
Total atoms total_atoms1839
Residues n_residues236
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 dmax65.7
Rg (real space) rg_real19.87
Rg uncertainty (real space) rg_real_error0.17
I(0) (real space) i0_real1.2460e+07
I(0) uncertainty (real space) i0_real_error1.3210e+05
Rg (reciprocal space) rg_reciprocal19.25
I(0) (reciprocal space) i0_reciprocal12530000.0000
Solution quality estimate total_estimate0.6683
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary23.1
Skewness Skewness skewness0.405
Kurtosis Kurtosis kurtosis-0.012
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha5.9640
Highest regularization parameter α highest_alpha2755000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.848; Stabil: 0.909; Sysdev: 0.000; Positv: 1.000; Valcen: 0.984; Smooth: 0.475

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2c23a_
Class classa — All alpha proteins
Fold Fold folda.118 — alpha-alpha superhelix
Superfamily Superfamily superfamilya.118.7 — 14-3-3 protein
Family Family familya.118.7.1 — 14-3-3 protein

CATH v4.4 (1 domains)

Domain ID domain_id2c23A00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology190 — Delta-Endotoxin; domain 1
Homologous superfamily homologous superfamily20 — 14-3-3 domain

8. Citations (1)

9. Files and Curves (10)