4zgn

Structure Cdc123 complexed with the C-terminal domain of eIF2gamma

Method: X-RAY DIFFRACTION Dmax: 92.5 Å Quality: GOOD

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

Cell division cycle protein 123

Schizosaccharomyces pombe

UniProt Q9P7N5

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 1–319 Not recorded Eukaryotic translation initiation factor 2 subunit gamma × 1 (P32481) ATP ADENOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8;298 K;25%PEG3350, 0.2MLiSO4, 0.1M TrispH8.0 Resolution 2.90 Å R-free 0.262

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 5 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CD123_SCHPO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 20–338; UniProt 1–319

Eukaryotic translation initiation factor 2 subunit gamma

Saccharomyces cerevisiae

UniProt P32481

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 410–527 Fragment:residues 410-527 Cell division cycle protein 123 × 1 (Q9P7N5) ATP ADENOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8;298 K;25%PEG3350, 0.2MLiSO4, 0.1M TrispH8.0 Resolution 2.90 Å R-free 0.262

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.

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

View Construct and Data Evidence
UniProt name IF2G_YEAST
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–118; UniProt 410–527

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 4zgn

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4zgn
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4zgn
Deposition date deposition_date2015-04-23
Structure title titleStructure Cdc123 complexed with the C-terminal domain of eIF2gamma
Keywords keywordsATP-grasp fold, cell cycle, eIF2 assembly; CELL CYCLE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.29
Radius of gyration Rg (electron density) rg_electron24.56
Forward intensity I(0) i031332000.00
Molecular weight molecular_weight44366.0 kDa
Excluded volume excluded_volume56090 ų
Envelope volume envelope_volume73037 ų
Hydration-shell volume shell_volume24925 ų
Envelope diameter envelope_diameter91.3
Shell Rg shell_rg31.38
Envelope Rg envelope_rg25.45
Shape Rg shape_rg24.54
Total Rg total_rg25.48
Total atoms total_atoms3125
Residues n_residues382
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 dmax92.5
Rg (real space) rg_real25.34
Rg uncertainty (real space) rg_real_error0.90
I(0) (real space) i0_real3.1330e+07
I(0) uncertainty (real space) i0_real_error4.5410e+05
Rg (reciprocal space) rg_reciprocal25.32
I(0) (reciprocal space) i0_reciprocal31330000.0000
Solution quality estimate total_estimate0.7577
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary26.4
Skewness Skewness skewness0.406
Kurtosis Kurtosis kurtosis-0.301
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8032000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.697; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.756; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id4zgnB00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology30 — Elongation Factor Tu (Ef-tu); domain 3
Homologous superfamily homologous superfamily10 — Translation factors

8. Citations (1)

9. Files and Curves (10)