2quq

Crystal Structure of the Essential Inner Kinetochore Protein Cep3p

Method: X-RAY DIFFRACTION Dmax: 81.8 Å Quality: GOOD

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

Centromere DNA-binding protein complex CBF3 subunit B

Saccharomyces cerevisiae

UniProt P40969

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 47–608 Fragment:residues 47-608 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;298 K;100 mM HEPES, 5% PEG 4000, 500 mM NaCl, pH 7.5, vapor diffusion, hanging drop, temperature 298K Resolution 2.80 Å R-free 0.285

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.

10 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CBF3B_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–562; UniProt 47–608

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 2quq

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2quq
Deposition date deposition_date2007-08-06
Structure title titleCrystal Structure of the Essential Inner Kinetochore Protein Cep3p
Keywords keywords;dimer, Centromere, Chromosomal protein, DNA-binding, Metal-binding, Nucleus, Phosphorylation, Zinc, PROTEIN BINDING, CELL CYCLE, DNA BINDING PROTEIN, STRUCTURAL PROTEIN ;; DNA BINDING PROTEIN, STRUCTURAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.36
Radius of gyration Rg (electron density) rg_electron24.24
Forward intensity I(0) i054821300.00
Molecular weight molecular_weight60787.0 kDa
Excluded volume excluded_volume77343 ų
Envelope volume envelope_volume91837 ų
Hydration-shell volume shell_volume30932 ų
Envelope diameter envelope_diameter85.0
Shell Rg shell_rg32.05
Envelope Rg envelope_rg24.63
Shape Rg shape_rg24.24
Total Rg total_rg25.11
Total atoms total_atoms4292
Residues n_residues517
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 dmax81.8
Rg (real space) rg_real25.28
Rg uncertainty (real space) rg_real_error0.47
I(0) (real space) i0_real5.4820e+07
I(0) uncertainty (real space) i0_real_error7.6680e+05
Rg (reciprocal space) rg_reciprocal25.31
I(0) (reciprocal space) i0_reciprocal54820000.0000
Solution quality estimate total_estimate0.8912
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary31.2
Skewness Skewness skewness0.283
Kurtosis Kurtosis kurtosis-0.286
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha11940000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.867; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.980

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)