3bxk

Crystal structure of the P/Q-type calcium channel (CaV2.1) IQ domain and CA2+calmodulin complex

Method: X-RAY DIFFRACTION Dmax: 76.0 Å Quality: EXCELLENT

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

Calmodulin

Rattus norvegicus

UniProt P62161

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 2–149 Not recorded Voltage-dependent P/Q-type calcium channel subunit alpha-1A peptide × 1 (O00555) CA CALCIUM ION × 4 SO4 SULFATE ION × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.55 Å R-free 0.267
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 2–149 Not recorded Voltage-dependent P/Q-type calcium channel subunit alpha-1A peptide × 1 (O00555) CA CALCIUM ION × 4 SO4 SULFATE ION × 2 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.55 Å R-free 0.267

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.

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

View Construct and Data Evidence
UniProt name CALM_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–148; UniProt 2–149 Author chain C; PDBConstruct 1–148; UniProt 2–149

Voltage-dependent P/Q-type calcium channel subunit alpha-1A peptide

OrganismNot specified

UniProt O00555

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 1955–1975 Not recorded Calmodulin × 1 (P62161) CA CALCIUM ION × 4 SO4 SULFATE ION × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.55 Å R-free 0.267
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 1955–1975 Not recorded Calmodulin × 1 (P62161) CA CALCIUM ION × 4 SO4 SULFATE ION × 2 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.55 Å R-free 0.267

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 CAC1A_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–21; UniProt 1955–1975 Author chain D; PDBConstruct 1–21; UniProt 1955–1975

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 3bxk

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id3bxk
Deposition date deposition_date2008-01-14
Structure title titleCrystal structure of the P/Q-type calcium channel (CaV2.1) IQ domain and CA2+calmodulin complex
Keywords keywords;ION CHANNEL, CALMODULIN, CALCIUM CHANNEL, IQ DOMAIN, FACILLITATION, INACTIVATION, CALCIUM-DEPENDENT, VOLTAGE-GATED, ROBETTA, SIMULATIONS; Acetylation, Methylation, Phosphoprotein, Calcium transport, Glycoprotein, Ion transport, Ionic channel, Membrane, Transmembrane, Transport, Voltage-gated channel, MEMBRANE PROTEIN, SIGNALING PROTEIN ;; MEMBRANE PROTEIN, SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.55
Radius of gyration Rg (electron density) rg_electron22.60
Forward intensity I(0) i025428100.00
Molecular weight molecular_weight36516.0 kDa
Excluded volume excluded_volume44740 ų
Envelope volume envelope_volume56148 ų
Hydration-shell volume shell_volume21389 ų
Envelope diameter envelope_diameter75.0
Shell Rg shell_rg28.63
Envelope Rg envelope_rg22.46
Shape Rg shape_rg22.59
Total Rg total_rg23.37
Total atoms total_atoms2531
Residues n_residues315
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 dmax76.0
Rg (real space) rg_real23.53
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real2.5430e+07
I(0) uncertainty (real space) i0_real_error3.3250e+05
Rg (reciprocal space) rg_reciprocal23.54
I(0) (reciprocal space) i0_reciprocal25430000.0000
Solution quality estimate total_estimate0.9006
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.7
Skewness Skewness skewness0.281
Kurtosis Kurtosis kurtosis-0.531
Angular range angular_range— – 0.3350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5439000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.910; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.977; Smooth: 0.996

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3bxka_
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.1 — EF-hand
Family Family familya.39.1.5 — Calmodulin-like
Domain ID domain_idd3bxkc_
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.1 — EF-hand
Family Family familya.39.1.5 — Calmodulin-like

CATH v4.4 (2 domains)

Domain ID domain_id3bxkA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand
Domain ID domain_id3bxkC00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand

8. Citations (1)

9. Files and Curves (10)