9jmj

Cryo-EM structure of the GD-BatCoV (BtCoV/Ii/GD/2014-422) RBD in complex with human DPP4

Method: ELECTRON MICROSCOPY Dmax: 138.7 Å Quality: GOOD

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

Dipeptidyl peptidase 4 soluble form,Isoform 1 of Immunoglobulin heavy constant gamma 1

Homo sapiens

UniProt P01857

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 3 其他Polymer 8 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 99–330 Chain B; UniProt 99–330 Chain C; UniProt 99–330 Fragment:RBD,RBD 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 7 beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 8 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.40 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.

134 other PDB entries and 162 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IGHG1_HUMAN
Isoform P01857-1
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 767–998; UniProt 99–330 Author chain C; PDBConstruct 767–998; UniProt 99–330 Author chain B; PDBConstruct 271–502; UniProt 99–330

Dipeptidyl peptidase 4 soluble form,Isoform 1 of Immunoglobulin heavy constant gamma 1

Homo sapiens

UniProt P27487

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 3 其他Polymer 8 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 39–766 Chain C; UniProt 39–766 Not recorded Spike glycoprotein,Isoform 1 of Immunoglobulin heavy constant gamma 1 × 1 (A0A2R4KP93,P01857) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 7 beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 8 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.40 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.

113 other PDB entries and 169 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DPP4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 25–752; UniProt 39–766 Author chain C; PDBConstruct 25–752; UniProt 39–766

Spike glycoprotein,Isoform 1 of Immunoglobulin heavy constant gamma 1

Homo sapiens

UniProt A0A2R4KP93

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 3 其他Polymer 8 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 371–610 Fragment:RBD,RBD Dipeptidyl peptidase 4 soluble form,Isoform 1 of Immunoglobulin heavy constant gamma 1 × 2 (P27487,P01857) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 7 beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 8 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.40 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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A2R4KP93_MERS
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 17–256; UniProt 371–610

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 9jmj

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9jmj
Deposition date deposition_date2024-09-20
Structure title titleCryo-EM structure of the GD-BatCoV (BtCoV/Ii/GD/2014-422) RBD in complex with human DPP4
Keywords keywordscomplex, VIRAL PROTEIN; VIRAL PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier42.69
Radius of gyration Rg (electron density) rg_electron42.39
Forward intensity I(0) i0557216000.00
Molecular weight molecular_weight195700.0 kDa
Excluded volume excluded_volume244920 ų
Envelope volume envelope_volume333900 ų
Hydration-shell volume shell_volume64991 ų
Envelope diameter envelope_diameter144.7
Shell Rg shell_rg48.22
Envelope Rg envelope_rg41.96
Shape Rg shape_rg42.32
Total Rg total_rg42.90
Total atoms total_atoms13813
Residues n_residues1656
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 dmax138.7
Rg (real space) rg_real42.69
Rg uncertainty (real space) rg_real_error0.93
I(0) (real space) i0_real5.5720e+08
I(0) uncertainty (real space) i0_real_error9.5090e+06
Rg (reciprocal space) rg_reciprocal42.69
I(0) (reciprocal space) i0_reciprocal557200000.0000
Solution quality estimate total_estimate0.8828
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary45.0
Skewness Skewness skewness0.302
Kurtosis Kurtosis kurtosis-0.565
Angular range angular_range— – 0.1850 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha67630000.0000
Real-space data points n_real_points38
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.897; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.781

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)