7m55

B6 Fab fragment bound to the MERS-CoV spike stem helix peptide

Method: X-RAY DIFFRACTION Dmax: 80.7 Å Quality: EXCELLENT

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

Spike glycoprotein stem helix peptide

OrganismNot specified

UniProt K9N5Q8

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1230–1244 Fragment:residues 1230-1244 of the spike glycoprotein B6 antigen binding fragment (Fab) heavy chain × 1 B6 antigen binding fragment (Fab) light chain × 1 GOL GLYCEROL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.2 M Magnesium Chloride and 20% (w/v) PEG3350 Resolution 1.40 Å R-free 0.200

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.

12 other PDB entries and 21 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPIKE_MERS1
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–15; UniProt 1230–1244

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 7m55

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7m55
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id7m55
Deposition date deposition_date2021-03-22
Structure title titleB6 Fab fragment bound to the MERS-CoV spike stem helix peptide
Keywords keywords;Broadly neutralizing antibody, Structural genomics, SSGCID, Center for Structural Genomics of Infectious Diseases, CSGID, ANTIVIRAL PROTEIN, Seattle Structural Genomics Center for Infectious Disease, IMMUNE SYSTEM ;; ANTIVIRAL PROTEIN, IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.25
Radius of gyration Rg (electron density) rg_electron24.32
Forward intensity I(0) i039944200.00
Molecular weight molecular_weight48295.0 kDa
Excluded volume excluded_volume60060 ų
Envelope volume envelope_volume71873 ų
Hydration-shell volume shell_volume24904 ų
Envelope diameter envelope_diameter82.9
Shell Rg shell_rg31.22
Envelope Rg envelope_rg24.06
Shape Rg shape_rg24.32
Total Rg total_rg25.10
Total atoms total_atoms3400
Residues n_residues449
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 dmax80.7
Rg (real space) rg_real25.24
Rg uncertainty (real space) rg_real_error0.52
I(0) (real space) i0_real3.9940e+07
I(0) uncertainty (real space) i0_real_error5.6670e+05
Rg (reciprocal space) rg_reciprocal25.25
I(0) (reciprocal space) i0_reciprocal39940000.0000
Solution quality estimate total_estimate0.9050
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.2
Skewness Skewness skewness0.314
Kurtosis Kurtosis kurtosis-0.450
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8287000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.933; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.973; Smooth: 0.987

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id7m55H01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins
Domain ID domain_id7m55H02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins
Domain ID domain_id7m55L01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins
Domain ID domain_id7m55L02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins

8. Citations (1)

9. Files and Curves (10)