5cqc

Crystal structure of the legionella pneumophila effector protein RavZ

Method: X-RAY DIFFRACTION Dmax: 84.0 Å Quality: GOOD

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

putative RavZ protein

Legionella pneumophila

UniProt Q5ZUV9

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 10–458 Not recorded BA BARIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.1;277.15 K;12% PEG 3350, 0.2 M BaCl2, 0.1 M MES Resolution 2.98 Å R-free 0.250

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.

7 other PDB entries and 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q5ZUV9_LEGPH
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–420; UniProt 10–458

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 5cqc

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id5cqc
Deposition date deposition_date2015-07-21
Structure title titleCrystal structure of the legionella pneumophila effector protein RavZ
Keywords keywordsUlp-family cysteine protease, autophagy inhibitor, PI3P binding domain, legionella pneumophila effector protein, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.09
Radius of gyration Rg (electron density) rg_electron23.46
Forward intensity I(0) i023806400.00
Molecular weight molecular_weight37054.0 kDa
Excluded volume excluded_volume46189 ų
Envelope volume envelope_volume56269 ų
Hydration-shell volume shell_volume21385 ų
Envelope diameter envelope_diameter91.8
Shell Rg shell_rg28.93
Envelope Rg envelope_rg23.81
Shape Rg shape_rg23.46
Total Rg total_rg24.17
Total atoms total_atoms2607
Residues n_residues352
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 dmax84.0
Rg (real space) rg_real24.24
Rg uncertainty (real space) rg_real_error0.72
I(0) (real space) i0_real2.3810e+07
I(0) uncertainty (real space) i0_real_error3.1760e+05
Rg (reciprocal space) rg_reciprocal24.20
I(0) (reciprocal space) i0_reciprocal23810000.0000
Solution quality estimate total_estimate0.7697
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.9
Skewness Skewness skewness0.515
Kurtosis Kurtosis kurtosis-0.177
Angular range angular_range— – 0.3300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4823000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.722; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.837; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)