9d55

Apo ACE full dimer 2 prepared by chameleon

Method: ELECTRON MICROSCOPY Dmax: 164.1 Å Quality: EXCELLENT

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

Angiotensin-converting enzyme

Homo sapiens

UniProt P12821

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Homooligomer Protein × 2 其他Polymer 12 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–1235 Chain B; UniProt 1–1235 Not recorded beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 ;beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose ; × 1 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 8 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 5 ELECTRON MICROSCOPY cryo-EM buffer:pH 5.5 cryo-EM vitrification conditions:Cryogen ETHANE;Grids prepared at NCCAT using Chameleon Resolution 3.15 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.

89 other PDB entries and 150 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ACE_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1235; UniProt 1–1235 Author chain B; PDBConstruct 1–1235; UniProt 1–1235

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 9d55

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9d55
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9d55
Deposition date deposition_date2024-08-13
Structure title titleApo ACE full dimer 2 prepared by chameleon
Keywords keywordshomodimer, zinc metalloprotease, HYDROLASE; HYDROLASE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier50.49
Radius of gyration Rg (electron density) rg_electron49.99
Forward intensity I(0) i01137480000.00
Molecular weight molecular_weight283240.0 kDa
Excluded volume excluded_volume354260 ų
Envelope volume envelope_volume493640 ų
Hydration-shell volume shell_volume79976 ų
Envelope diameter envelope_diameter158.5
Shell Rg shell_rg56.18
Envelope Rg envelope_rg48.72
Shape Rg shape_rg49.95
Total Rg total_rg50.31
Total atoms total_atoms20016
Residues n_residues2400
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 dmax164.1
Rg (real space) rg_real50.39
Rg uncertainty (real space) rg_real_error1.52
I(0) (real space) i0_real1.1370e+09
I(0) uncertainty (real space) i0_real_error2.4100e+07
Rg (reciprocal space) rg_reciprocal50.55
I(0) (reciprocal space) i0_reciprocal1138000000.0000
Solution quality estimate total_estimate0.9017
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary68.8
Skewness Skewness skewness0.129
Kurtosis Kurtosis kurtosis-0.758
Angular range angular_range— – 0.1550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha278200000.0000
Real-space data points n_real_points32
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.927; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.944

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (2)

9. Files and Curves (10)