4bme

Crystal structure of the N terminal domain of human Galectin 8, F19Y mutant

Method: X-RAY DIFFRACTION Dmax: 76.3 Å Quality: GOOD

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

GALECTIN-8

HOMO SAPIENS

UniProt O00214

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Monomer Protein × 1 其他Polymer 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 4–155 Fragment:N TERMINAL DOMAIN, RESIDUES 4-155 Mutation:YES beta-D-galactopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:30% W/V PEG 4000, 100 MM MES SODIUM SALT (PH 6.5) Resolution 2.00 Å R-free 0.241
2 Other combination Monomer Protein × 1 其他Polymer 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 4–155 Fragment:N TERMINAL DOMAIN, RESIDUES 4-155 Mutation:YES beta-D-galactopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:30% W/V PEG 4000, 100 MM MES SODIUM SALT (PH 6.5) Resolution 2.00 Å R-free 0.241

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.

36 other PDB entries and 54 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LEG8_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–152; UniProt 4–155 Author chain B; PDBConstruct 1–152; UniProt 4–155

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 4bme

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4bme
Deposition date deposition_date2013-05-07
Structure title titleCrystal structure of the N terminal domain of human Galectin 8, F19Y mutant
Keywords keywordsSUGAR BINDING PROTEIN, CARBOHYDRATE RECOGNITION; SUGAR BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.77
Radius of gyration Rg (electron density) rg_electron21.86
Forward intensity I(0) i018741200.00
Molecular weight molecular_weight33833.0 kDa
Excluded volume excluded_volume42804 ų
Envelope volume envelope_volume50811 ų
Hydration-shell volume shell_volume20106 ų
Envelope diameter envelope_diameter78.0
Shell Rg shell_rg27.80
Envelope Rg envelope_rg22.03
Shape Rg shape_rg21.84
Total Rg total_rg22.74
Total atoms total_atoms2388
Residues n_residues293
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 dmax76.3
Rg (real space) rg_real22.83
Rg uncertainty (real space) rg_real_error0.49
I(0) (real space) i0_real1.8740e+07
I(0) uncertainty (real space) i0_real_error2.3310e+05
Rg (reciprocal space) rg_reciprocal22.82
I(0) (reciprocal space) i0_reciprocal18740000.0000
Solution quality estimate total_estimate0.8740
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.1
Skewness Skewness skewness0.407
Kurtosis Kurtosis kurtosis-0.432
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4270000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.802; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.957; Smooth: 0.994

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4bmea_
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.0 — automated matches
Domain ID domain_idd4bmeb_
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.0 — automated matches

CATH v4.4 (2 domains)

Domain ID domain_id4bmeA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily200
Domain ID domain_id4bmeB00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily200

8. Citations (1)

9. Files and Curves (10)