8tzf

Structure of full length LRRK2 bound to GZD-824 (I2020T mutant)

Method: ELECTRON MICROSCOPY Dmax: 142.6 Å Quality: REASONABLE

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

Leucine-rich repeat serine/threonine-protein kinase 2

Homo sapiens

UniProt Q5S007

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 1–2527 Mutation:I2020T designed ankyrin repeat proteins E11 × 1 GDP GUANOSINE-5'-DIPHOSPHATE × 1 T3X 4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}-3-[(1H-pyrazolo[3,4-b]pyridin-5-yl)ethynyl]benzamide × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.40 Å

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.

40 other PDB entries and 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LRRK2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–2527; UniProt 1–2527

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 8tzf

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8tzf
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8tzf
Deposition date deposition_date2023-08-26
Structure title titleStructure of full length LRRK2 bound to GZD-824 (I2020T mutant)
Keywords keywordsKinase inhibitors, Kinase, GTPases, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier43.88
Radius of gyration Rg (electron density) rg_electron42.91
Forward intensity I(0) i0445599000.00
Molecular weight molecular_weight172620.0 kDa
Excluded volume excluded_volume215920 ų
Envelope volume envelope_volume325680 ų
Hydration-shell volume shell_volume64153 ų
Envelope diameter envelope_diameter145.4
Shell Rg shell_rg47.36
Envelope Rg envelope_rg42.73
Shape Rg shape_rg42.98
Total Rg total_rg42.88
Total atoms total_atoms12170
Residues n_residues1673
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 dmax142.6
Rg (real space) rg_real43.89
Rg uncertainty (real space) rg_real_error1.04
I(0) (real space) i0_real4.4560e+08
I(0) uncertainty (real space) i0_real_error8.2830e+06
Rg (reciprocal space) rg_reciprocal43.88
I(0) (reciprocal space) i0_reciprocal445600000.0000
Solution quality estimate total_estimate0.6583
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary51.5
Skewness Skewness skewness0.305
Kurtosis Kurtosis kurtosis-0.484
Angular range angular_range— – 0.1800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha42000000.0000
Real-space data points n_real_points37
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.928; Stabil: 1.000; Sysdev: 0.032; Positv: 1.000; Valcen: 0.997; Smooth: 0.674

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)