8wyu

Open Falcilysin, from MK-4815-treated dataset

Method: ELECTRON MICROSCOPY Dmax: 98.2 Å Quality: EXCELLENT

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

Falcilysin

Plasmodium falciparum 3D7

UniProt Q76NL8

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 61–1193 Not recorded ZN ZINC ION × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5;20 mM Na HEPES, 300 mM NaCl, 0.5 mM TCEP, pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.20 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.

14 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FCLN_PLAF7
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1133; UniProt 61–1193

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 8wyu

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8wyu
Deposition date deposition_date2023-10-31
Structure title titleOpen Falcilysin, from MK-4815-treated dataset
Keywords keywordsfalcilysin open conformation, HYDROLASE; HYDROLASE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier33.34
Radius of gyration Rg (electron density) rg_electron32.22
Forward intensity I(0) i0230180000.00
Molecular weight molecular_weight125020.0 kDa
Excluded volume excluded_volume158100 ų
Envelope volume envelope_volume204650 ų
Hydration-shell volume shell_volume51462 ų
Envelope diameter envelope_diameter104.0
Shell Rg shell_rg40.75
Envelope Rg envelope_rg31.06
Shape Rg shape_rg32.21
Total Rg total_rg32.98
Total atoms total_atoms8819
Residues n_residues1072
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 dmax98.2
Rg (real space) rg_real33.11
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real2.3020e+08
I(0) uncertainty (real space) i0_real_error3.5130e+06
Rg (reciprocal space) rg_reciprocal33.25
I(0) (reciprocal space) i0_reciprocal230200000.0000
Solution quality estimate total_estimate0.9000
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary48.1
Skewness Skewness skewness-0.008
Kurtosis Kurtosis kurtosis-0.519
Angular range angular_range— – 0.2350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha37930000.0000
Real-space data points n_real_points48
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.935; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.973; Smooth: 0.917

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)