9iis

GDP-fucose pyrophosphorylase part of FKP with a SUMO tag

Method: X-RAY DIFFRACTION Dmax: 93.6 Å Quality: REASONABLE

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

Ubiquitin-like protein SMT3,L-fucokinase/L-fucose-1-P guanylyltransferase

Bacteroides fragilis

UniProt Q12306

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–98 Not recorded EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;295 K;PEG 3350, ammonium acetate, HEPES Resolution 2.36 Å R-free 0.254

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.

95 other PDB entries and 116 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SMT3_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 22–119; UniProt 1–98

Ubiquitin-like protein SMT3,L-fucokinase/L-fucose-1-P guanylyltransferase

Bacteroides fragilis

UniProt Q58T34

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–496 Not recorded EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;295 K;PEG 3350, ammonium acetate, HEPES Resolution 2.36 Å R-free 0.254

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 Q58T34_BACFG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 122–617; UniProt 1–496

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 9iis

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9iis
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9iis
Deposition date deposition_date2024-06-21
Structure title titleGDP-fucose pyrophosphorylase part of FKP with a SUMO tag
Keywords keywordsGDP-fucose, pyrophosphorylase, HEPES, beta-helix, SUMO, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.94
Radius of gyration Rg (electron density) rg_electron27.04
Forward intensity I(0) i062327200.00
Molecular weight molecular_weight62295.0 kDa
Excluded volume excluded_volume78301 ų
Envelope volume envelope_volume98677 ų
Hydration-shell volume shell_volume31159 ų
Envelope diameter envelope_diameter97.5
Shell Rg shell_rg33.67
Envelope Rg envelope_rg27.09
Shape Rg shape_rg27.02
Total Rg total_rg27.82
Total atoms total_atoms4390
Residues n_residues551
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 dmax93.6
Rg (real space) rg_real27.93
Rg uncertainty (real space) rg_real_error0.61
I(0) (real space) i0_real6.2330e+07
I(0) uncertainty (real space) i0_real_error9.0770e+05
Rg (reciprocal space) rg_reciprocal27.93
I(0) (reciprocal space) i0_reciprocal62330000.0000
Solution quality estimate total_estimate0.6773
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.9
Skewness Skewness skewness0.320
Kurtosis Kurtosis kurtosis-0.334
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha15940000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.870; Stabil: 1.000; Sysdev: 0.075; Positv: 1.000; Valcen: 0.983; Smooth: 0.982

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)