3im3

Crystal structure of PKA RI alpha dimerization/docking domain

Method: X-RAY DIFFRACTION Dmax: 52.0 Å Quality: GOOD

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

cAMP-dependent protein kinase type I-alpha regulatory subunit

Bos taurus

UniProt P00514

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 13–62 Fragment:Dimerization and docking domain: UNP residues 13-62 FMT FORMIC ACID × 4 X-RAY DIFFRACTION X-ray crystallization conditions:MICROBATCH;pH 9;298 K;30% PEG 3350, 0.2 mM Sodium formate, 0.1 M Bis-Tris propane pH 9.0, MICROBATCH, temperature 298K Resolution 2.00 Å R-free 0.249

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.

25 other PDB entries and 46 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KAP0_BOVIN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–50; UniProt 13–62

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 3im3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3im3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3im3
Deposition date deposition_date2009-08-09
Structure title titleCrystal structure of PKA RI alpha dimerization/docking domain
Keywords keywords;helix-turn-helix, Acetylation, cAMP, cAMP-binding, Disulfide bond, Nucleotide-binding, Phosphoprotein, STRUCTURAL PROTEIN, SIGNALING PROTEIN ;; STRUCTURAL PROTEIN, SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier14.93
Radius of gyration Rg (electron density) rg_electron13.62
Forward intensity I(0) i0881323.00
Molecular weight molecular_weight6071.0 kDa
Excluded volume excluded_volume7623 ų
Envelope volume envelope_volume9961 ų
Hydration-shell volume shell_volume6988 ų
Envelope diameter envelope_diameter50.3
Shell Rg shell_rg17.71
Envelope Rg envelope_rg14.07
Shape Rg shape_rg13.55
Total Rg total_rg14.94
Total atoms total_atoms425
Residues n_residues50
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 dmax52.0
Rg (real space) rg_real14.99
Rg uncertainty (real space) rg_real_error0.42
I(0) (real space) i0_real8.8130e+05
I(0) uncertainty (real space) i0_real_error9.9060e+03
Rg (reciprocal space) rg_reciprocal14.98
I(0) (reciprocal space) i0_reciprocal881300.0000
Solution quality estimate total_estimate0.8724
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary15.8
Skewness Skewness skewness0.283
Kurtosis Kurtosis kurtosis-0.457
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha67610.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.880; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.789; Smooth: 0.907

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd3im3a_
Class classa — All alpha proteins
Fold Fold folda.31 — Dimerization-anchoring domain of cAMP-dependent PK regulatory subunit
Superfamily Superfamily superfamilya.31.1 — Dimerization-anchoring domain of cAMP-dependent PK regulatory subunit
Family Family familya.31.1.1 — Dimerization-anchoring domain of cAMP-dependent PK regulatory subunit

CATH v4.4 (1 domains)

Domain ID domain_id3im3A00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology890 — cAMP-dependent Protein Kinase, Chain A
Homologous superfamily homologous superfamily10 — cAMP-dependent protein kinase regulatory subunit, dimerization-anchoring domain

8. Citations (1)

9. Files and Curves (10)