7s48

PAK4cat in complex with Integrin beta5 760-770 peptide

Method: X-RAY DIFFRACTION Dmax: 63.6 Å Quality: GOOD

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

Serine/threonine-protein kinase PAK 4

Homo sapiens

UniProt O96013

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 109–426 Non-standard monomer:Yes (specific site not provided by mmCIF) Integrin beta-5 × 1 (P18084) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M Tris-HCl (pH 8.5) and 0.5 M tri-sodium citrate Resolution 1.90 Å R-free 0.222

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.

46 other PDB entries and 61 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PAK4_HUMAN
Isoform O96013-2
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 29–346; UniProt 109–426

Integrin beta-5

OrganismNot specified

UniProt P18084

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 760–770 Not recorded Serine/threonine-protein kinase PAK 4 × 1 (O96013) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M Tris-HCl (pH 8.5) and 0.5 M tri-sodium citrate Resolution 1.90 Å R-free 0.222

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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ITB5_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–11; UniProt 760–770

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 7s48

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7s48
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7s48
Deposition date deposition_date2021-09-08
Structure title titlePAK4cat in complex with Integrin beta5 760-770 peptide
Keywords keywordsserine/threonine kinase, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.21
Radius of gyration Rg (electron density) rg_electron19.19
Forward intensity I(0) i019041800.00
Molecular weight molecular_weight33591.0 kDa
Excluded volume excluded_volume42333 ų
Envelope volume envelope_volume48574 ų
Hydration-shell volume shell_volume21004 ų
Envelope diameter envelope_diameter62.6
Shell Rg shell_rg25.68
Envelope Rg envelope_rg19.35
Shape Rg shape_rg19.20
Total Rg total_rg20.05
Total atoms total_atoms2357
Residues n_residues296
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 dmax63.6
Rg (real space) rg_real20.11
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real1.9040e+07
I(0) uncertainty (real space) i0_real_error2.5180e+05
Rg (reciprocal space) rg_reciprocal20.13
I(0) (reciprocal space) i0_reciprocal19040000.0000
Solution quality estimate total_estimate0.8965
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.5
Skewness Skewness skewness0.201
Kurtosis Kurtosis kurtosis-0.395
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5472000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.891; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.985

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)