1ctd

DETERMINATION OF THE SOLUTION STRUCTURE OF A SYNTHETIC TWO-SITE CALCIUM-BINDING HOMODIMERIC PROTEIN DOMAIN BY NMR SPECTROSCOPY

Method: SOLUTION NMR Dmax: 45.8 Å Quality: REASONABLE

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

TROPONIN C SITE III - SITE III HOMODIMER

OrganismNot specified

UniProt P02588

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 93–126 Chain B; UniProt 93–126 Non-standard monomer:Yes (specific site not provided by mmCIF) CA CALCIUM ION × 2 SOLUTION NMR mmCIF provides none of the parsed experimental conditions 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.

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

View Construct and Data Evidence
UniProt name TPCS_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–35; UniProt 93–126 Author chain B; PDBConstruct 2–35; UniProt 93–126

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 1ctd

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1ctd
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1ctd
Deposition date deposition_date1992-11-12
Structure title titleDETERMINATION OF THE SOLUTION STRUCTURE OF A SYNTHETIC TWO-SITE CALCIUM-BINDING HOMODIMERIC PROTEIN DOMAIN BY NMR SPECTROSCOPY
Keywords keywordsMUSCLE PROTEIN; MUSCLE PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier12.42
Radius of gyration Rg (electron density) rg_electron11.74
Forward intensity I(0) i046488900.00
Molecular weight molecular_weight54674.0 kDa
Excluded volume excluded_volume67855 ų
Envelope volume envelope_volume19412 ų
Hydration-shell volume shell_volume12011 ų
Envelope diameter envelope_diameter51.0
Shell Rg shell_rg19.60
Envelope Rg envelope_rg14.24
Shape Rg shape_rg11.71
Total Rg total_rg12.35
Total atoms total_atoms4662
Residues n_residues476
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 dmax45.8
Rg (real space) rg_real12.38
Rg uncertainty (real space) rg_real_error0.42
I(0) (real space) i0_real4.6490e+07
I(0) uncertainty (real space) i0_real_error5.3600e+05
Rg (reciprocal space) rg_reciprocal12.38
I(0) (reciprocal space) i0_reciprocal46490000.0000
Solution quality estimate total_estimate0.7445
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary16.2
Skewness Skewness skewness0.235
Kurtosis Kurtosis kurtosis-0.017
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha89440.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.577; Stabil: 0.996; Sysdev: 1.000; Positv: 1.000; Valcen: 0.954; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1ctda_
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_idd1ctdb_
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

8. Citations (1)

9. Files and Curves (10)