9h2q

Stabilized complex of Chlamydia trachomatic efector CT622 in complex with human WD40 domain of ATG16L1

Method: ELECTRON MICROSCOPY Dmax: 96.1 Å Quality: GOOD

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

Maltose/maltodextrin-binding periplasmic protein,CHLPN 76 kD protein-like

Chlamydia trachomatis

UniProt A0A0H2X2S1

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 361–651 Not recorded Autophagy-related protein 16-1 × 1 (Q676U5) ELECTRON MICROSCOPY cryo-EM buffer:pH 6 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 3.80 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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name A0A0H2X2S1_CHLTA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 384–674; UniProt 361–651

Maltose/maltodextrin-binding periplasmic protein,CHLPN 76 kD protein-like

Chlamydia trachomatis

UniProt P0AEY0

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 27–395 Not recorded Autophagy-related protein 16-1 × 1 (Q676U5) ELECTRON MICROSCOPY cryo-EM buffer:pH 6 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 3.80 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.

109 other PDB entries and 148 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MALE_ECO57
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 7–375; UniProt 27–395

Autophagy-related protein 16-1

Homo sapiens

UniProt Q676U5

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 303–607 Not recorded Maltose/maltodextrin-binding periplasmic protein,CHLPN 76 kD protein-like × 1 (P0AEY0,A0A0H2X2S1) ELECTRON MICROSCOPY cryo-EM buffer:pH 6 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 3.80 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.

13 other PDB entries and 24 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A16L1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 5–309; UniProt 303–607

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 9h2q

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9h2q
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9h2q
Deposition date deposition_date2024-10-14
Structure title titleStabilized complex of Chlamydia trachomatic efector CT622 in complex with human WD40 domain of ATG16L1
Keywords keywordsEffector protein, autophagy, xenophagy, infection, PROTEIN TRANSPORT; PROTEIN TRANSPORT
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier28.45
Radius of gyration Rg (electron density) rg_electron28.17
Forward intensity I(0) i058017800.00
Molecular weight molecular_weight58324.0 kDa
Excluded volume excluded_volume72509 ų
Envelope volume envelope_volume91149 ų
Hydration-shell volume shell_volume28491 ų
Envelope diameter envelope_diameter99.0
Shell Rg shell_rg33.80
Envelope Rg envelope_rg28.26
Shape Rg shape_rg28.19
Total Rg total_rg28.68
Total atoms total_atoms4102
Residues n_residues542
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 dmax96.1
Rg (real space) rg_real28.71
Rg uncertainty (real space) rg_real_error0.82
I(0) (real space) i0_real5.8020e+07
I(0) uncertainty (real space) i0_real_error9.5180e+05
Rg (reciprocal space) rg_reciprocal28.63
I(0) (reciprocal space) i0_reciprocal58010000.0000
Solution quality estimate total_estimate0.8388
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.4
Skewness Skewness skewness0.534
Kurtosis Kurtosis kurtosis-0.281
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16160000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.769; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.823; Smooth: 0.771

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (2)

9. Files and Curves (10)