9nc1

MicroED structure of papain-E-64 complex from microcrystals soaked with protease inhibitor cocktail

Method: ELECTRON CRYSTALLOGRAPHY Dmax: 52.1 Å Quality: REASONABLE

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

Papain

OrganismNot specified

UniProt P00784

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 134–345 Not recorded E64 N-[N-[1-HYDROXYCARBOXYETHYL-CARBONYL]LEUCYLAMINO-BUTYL]-GUANIDINE × 1 ELECTRON CRYSTALLOGRAPHY cryo-EM buffer:pH 7 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.40 Å R-free 0.261

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.

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

View Construct and Data Evidence
UniProt name PAPA1_CARPA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–212; UniProt 134–345

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 9nc1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9nc1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9nc1
Deposition date deposition_date2025-02-14
Structure title titleMicroED structure of papain-E-64 complex from microcrystals soaked with protease inhibitor cocktail
Keywords keywordsInhibitor, Complex, MicroED, Cocktail, HYDROLASE-INHIBITOR complex; HYDROLASE/INHIBITOR
Experimental Method methodELECTRON CRYSTALLOGRAPHY

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

Radius of gyration Rg (Guinier) rg_guinier17.37
Radius of gyration Rg (electron density) rg_electron16.18
Forward intensity I(0) i010470300.00
Molecular weight molecular_weight23795.0 kDa
Excluded volume excluded_volume29633 ų
Envelope volume envelope_volume32248 ų
Hydration-shell volume shell_volume16473 ų
Envelope diameter envelope_diameter55.9
Shell Rg shell_rg22.56
Envelope Rg envelope_rg16.53
Shape Rg shape_rg16.17
Total Rg total_rg17.24
Total atoms total_atoms1680
Residues n_residues212
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 dmax52.1
Rg (real space) rg_real17.31
Rg uncertainty (real space) rg_real_error0.07
I(0) (real space) i0_real1.0140e+07
I(0) uncertainty (real space) i0_real_error8.0970e+04
Rg (reciprocal space) rg_reciprocal17.28
I(0) (reciprocal space) i0_reciprocal10470000.0000
Solution quality estimate total_estimate0.6997
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary21.9
Skewness Skewness skewness0.197
Kurtosis Kurtosis kurtosis-0.357
Angular range angular_range— – 0.4600 −1
Current regularization parameter α current_alpha10.9000
Highest regularization parameter α highest_alpha2667000.0000
Real-space data points n_real_points77
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.946; Stabil: 0.921; Sysdev: 0.000; Positv: 1.000; Valcen: 0.988; Smooth: 0.526

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (2)

9. Files and Curves (10)