5sbu

CD44 PanDDA analysis group deposition -- The hyaluronan-binding domain of CD44 in complex with Z839988838

Method: X-RAY DIFFRACTION Dmax: 51.2 Å Quality: REASONABLE

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

CD44 antigen

Mus musculus

UniProt P15379

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 23–172 Not recorded 8C2 N-[(3,5-dimethyl-1H-pyrazol-4-yl)methyl]cyclohexanamine × 1 PGE TRIETHYLENE GLYCOL × 1 DMS DIMETHYL SULFOXIDE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;200mM ammonium sulphate, 100mM MES, 24% PEG 5,000 MME Resolution 1.04 Å R-free 0.179

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.

52 other PDB entries and 52 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CD44_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–152; UniProt 23–172

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 5sbu

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id5sbu
Deposition date deposition_date2021-09-14
Structure title titleCD44 PanDDA analysis group deposition -- The hyaluronan-binding domain of CD44 in complex with Z839988838
Keywords keywordsSGC - Diamond I04-1 fragment screening, PanDDA, XChemExplorer, antigen, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.87
Radius of gyration Rg (electron density) rg_electron14.76
Forward intensity I(0) i06074700.00
Molecular weight molecular_weight17199.0 kDa
Excluded volume excluded_volume21222 ų
Envelope volume envelope_volume23404 ų
Hydration-shell volume shell_volume13420 ų
Envelope diameter envelope_diameter51.0
Shell Rg shell_rg20.57
Envelope Rg envelope_rg15.07
Shape Rg shape_rg14.73
Total Rg total_rg15.86
Total atoms total_atoms1204
Residues n_residues150
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 dmax51.2
Rg (real space) rg_real15.77
Rg uncertainty (real space) rg_real_error0.23
I(0) (real space) i0_real6.0750e+06
I(0) uncertainty (real space) i0_real_error7.0870e+04
Rg (reciprocal space) rg_reciprocal15.78
I(0) (reciprocal space) i0_reciprocal6075000.0000
Solution quality estimate total_estimate0.7131
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.1
Skewness Skewness skewness0.173
Kurtosis Kurtosis kurtosis-0.337
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1105000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.837; Stabil: 1.000; Sysdev: 0.256; Positv: 1.000; Valcen: 0.998; Smooth: 0.988

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)