7nt3

Crystal structure of SARS CoV2 main protease in complex with FSCU015

Method: X-RAY DIFFRACTION Dmax: 82.4 Å Quality: EXCELLENT

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

3C-like proteinase

Severe acute respiratory syndrome coronavirus 2

UniProt P0DTC1

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 3264–3569 Chain B; UniProt 3264–3569 Not recorded DMS DIMETHYL SULFOXIDE × 4 UQZ ~{N}-[(1~{S})-2-(1,3-benzodioxol-5-ylmethylamino)-1-(3-hydroxyphenyl)-2-oxidanylidene-ethyl]-~{N}-propyl-prop-2-enamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.1 M MES pH 6.5 15% w/v PEG 6000 5% v/v MPD Compound stock FSP006 100 mM in 100% DMSO Crystals were soaked for 3 hours with final concentration of 10 mM FSCU015 by adding the stock to crystallisation drops in a 1/10 ratio yielding 10% (V/V) final DMSO concentration. Resolution 2.33 Å R-free 0.271

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.

440 other PDB entries and 508 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name R1A_SARS2
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–306; UniProt 3264–3569 Author chain B; PDBConstruct 1–306; UniProt 3264–3569

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 7nt3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7nt3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7nt3
Deposition date deposition_date2021-03-08
Structure title titleCrystal structure of SARS CoV2 main protease in complex with FSCU015
Keywords keywordsProtease, Complex, VIRAL PROTEIN; VIRAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.58
Radius of gyration Rg (electron density) rg_electron25.54
Forward intensity I(0) i076444500.00
Molecular weight molecular_weight67657.0 kDa
Excluded volume excluded_volume84323 ų
Envelope volume envelope_volume101600 ų
Hydration-shell volume shell_volume32749 ų
Envelope diameter envelope_diameter86.0
Shell Rg shell_rg33.17
Envelope Rg envelope_rg25.70
Shape Rg shape_rg25.53
Total Rg total_rg26.40
Total atoms total_atoms4736
Residues n_residues607
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 dmax82.4
Rg (real space) rg_real26.44
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real7.6440e+07
I(0) uncertainty (real space) i0_real_error1.1160e+06
Rg (reciprocal space) rg_reciprocal26.48
I(0) (reciprocal space) i0_reciprocal76450000.0000
Solution quality estimate total_estimate0.9079
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary35.7
Skewness Skewness skewness0.150
Kurtosis Kurtosis kurtosis-0.554
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha37880000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.940; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.983

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd7nt3a_
Class classb — All beta proteins
Fold Fold foldb.47 — Trypsin-like serine proteases
Superfamily Superfamily superfamilyb.47.1 — Trypsin-like serine proteases
Family Family familyb.47.1.4 — Viral cysteine protease of trypsin fold
Domain ID domain_idd7nt3b_
Class classb — All beta proteins
Fold Fold foldb.47 — Trypsin-like serine proteases
Superfamily Superfamily superfamilyb.47.1 — Trypsin-like serine proteases
Family Family familyb.47.1.4 — Viral cysteine protease of trypsin fold

CATH v4.4 (4 domains)

Domain ID domain_id7nt3A01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id7nt3A02
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1840 — main proteinase (3clpro) structure, domain 3
Homologous superfamily homologous superfamily10 — main proteinase (3clpro) structure, domain 3
Domain ID domain_id7nt3B01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id7nt3B02
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1840 — main proteinase (3clpro) structure, domain 3
Homologous superfamily homologous superfamily10 — main proteinase (3clpro) structure, domain 3

8. Citations (1)

9. Files and Curves (10)