5iig

Structure of the SPX-TTM domain fragment of the yeast inorganic polyphophate polymerase Vtc4 (form A).

Method: X-RAY DIFFRACTION Dmax: 107.2 Å Quality: REASONABLE

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

Vacuolar transporter chaperone 4

Saccharomyces cerevisiae

UniProt P47075

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 2–480 Fragment:SPX domain, UNP residues 2-480 Mutation:E426N SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;298 K;0.1M HEPES, 1.5M Li2SO4 Resolution 2.99 Å R-free 0.273

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 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VTC4_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–483; UniProt 2–480

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 5iig

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5iig
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5iig
Deposition date deposition_date2016-03-01
Structure title titleStructure of the SPX-TTM domain fragment of the yeast inorganic polyphophate polymerase Vtc4 (form A).
Keywords keywordshelical bundle, alpha-helical hairpin, inositol phosphate binding, protein-protein interaction, chaperone, transferase; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.83
Radius of gyration Rg (electron density) rg_electron31.02
Forward intensity I(0) i048603900.00
Molecular weight molecular_weight54779.0 kDa
Excluded volume excluded_volume68749 ų
Envelope volume envelope_volume91157 ų
Hydration-shell volume shell_volume27497 ų
Envelope diameter envelope_diameter112.6
Shell Rg shell_rg33.93
Envelope Rg envelope_rg31.18
Shape Rg shape_rg31.03
Total Rg total_rg31.31
Total atoms total_atoms3871
Residues n_residues467
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 dmax107.2
Rg (real space) rg_real31.36
Rg uncertainty (real space) rg_real_error1.06
I(0) (real space) i0_real4.8600e+07
I(0) uncertainty (real space) i0_real_error8.3880e+05
Rg (reciprocal space) rg_reciprocal31.13
I(0) (reciprocal space) i0_reciprocal48590000.0000
Solution quality estimate total_estimate0.7422
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.3
Skewness Skewness skewness0.705
Kurtosis Kurtosis kurtosis-0.191
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12970000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.513; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.452; Smooth: 0.653

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id5iigA02
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology100 — mRNA Triphosphatase Cet1; Chain A
Homologous superfamily homologous superfamily30 — VTC, catalytic tunnel domain

8. Citations (1)

9. Files and Curves (10)