9ms8

PTCH1 in complex with Fab6H3

Method: ELECTRON MICROSCOPY Dmax: 127.6 Å Quality: GOOD

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

Protein patched homolog 1

Homo sapiens

UniProt Q13635

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 1–618 Chain A; UniProt 721–1188 Not recorded 6H3 Fab light chain × 1 6H3 Fab heavy chain × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.73 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.

15 other PDB entries and 17 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PTC1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–618; UniProt 1–618 Author chain A; PDBConstruct 619–1086; UniProt 721–1188

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 9ms8

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9ms8
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9ms8
Deposition date deposition_date2025-01-09
Structure title titlePTCH1 in complex with Fab6H3
Keywords keywordsPTCH1, Antibody, hedgehog signaling, cryo-EM, membrane protein., MEMBRANE PROTEIN-IMMUNE SYSTEM complex; MEMBRANE PROTEIN/IMMUNE SYSTEM
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier39.24
Radius of gyration Rg (electron density) rg_electron39.09
Forward intensity I(0) i0241164000.00
Molecular weight molecular_weight131750.0 kDa
Excluded volume excluded_volume167040 ų
Envelope volume envelope_volume221520 ų
Hydration-shell volume shell_volume48421 ų
Envelope diameter envelope_diameter132.7
Shell Rg shell_rg43.29
Envelope Rg envelope_rg39.09
Shape Rg shape_rg39.05
Total Rg total_rg39.51
Total atoms total_atoms9290
Residues n_residues1189
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 dmax127.6
Rg (real space) rg_real39.37
Rg uncertainty (real space) rg_real_error0.86
I(0) (real space) i0_real2.4120e+08
I(0) uncertainty (real space) i0_real_error3.8590e+06
Rg (reciprocal space) rg_reciprocal39.30
I(0) (reciprocal space) i0_reciprocal241100000.0000
Solution quality estimate total_estimate0.8727
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary38.3
Skewness Skewness skewness0.342
Kurtosis Kurtosis kurtosis-0.558
Angular range angular_range— – 0.2000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha35900000.0000
Real-space data points n_real_points41
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.922; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.951; Smooth: 0.624

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)