1h5g

X-ray induced reduction of horseradish peroxidase C1A Compound III (33-44% dose)

Method: X-RAY DIFFRACTION Dmax: 65.0 Å Quality: REASONABLE

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

PEROXIDASE C1A

ARMORACIA RUSTICANA

UniProt P00433

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 31–338 Not recorded HEM PROTOPORPHYRIN IX CONTAINING FE × 1 ACT ACETATE ION × 1 CA CALCIUM ION × 2 PEO HYDROGEN PEROXIDE × 4 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;20% (W/V) PEG 4000, 0.2 M CALCIUM ACETATE, 0.1 M CACODYLATE BUFFER, PH 6.5 Resolution 1.60 Å R-free 0.223

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.

31 other PDB entries and 34 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PERA_ARMRU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–308; UniProt 31–338

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 1h5g

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1h5g
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1h5g
Deposition date deposition_date2001-05-21
Structure title titleX-ray induced reduction of horseradish peroxidase C1A Compound III (33-44% dose)
Keywords keywordsOXIDOREDUCTASE, PEROXIDASE, HORSERADISH, COMPOUND III, OXYPEROXIDASE, X-RAY INDUCED REDUCTION; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.05
Radius of gyration Rg (electron density) rg_electron18.99
Forward intensity I(0) i021576200.00
Molecular weight molecular_weight34591.0 kDa
Excluded volume excluded_volume42922 ų
Envelope volume envelope_volume47228 ų
Hydration-shell volume shell_volume20644 ų
Envelope diameter envelope_diameter66.7
Shell Rg shell_rg25.55
Envelope Rg envelope_rg19.29
Shape Rg shape_rg18.97
Total Rg total_rg19.91
Total atoms total_atoms2426
Residues n_residues306
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 dmax65.0
Rg (real space) rg_real19.98
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real2.1580e+07
I(0) uncertainty (real space) i0_real_error2.4680e+05
Rg (reciprocal space) rg_reciprocal20.00
I(0) (reciprocal space) i0_reciprocal21580000.0000
Solution quality estimate total_estimate0.6760
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.1
Skewness Skewness skewness0.267
Kurtosis Kurtosis kurtosis-0.308
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5176000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.856; Stabil: 0.999; Sysdev: 0.406; Positv: 1.000; Valcen: 0.998; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1h5ga_
Class classa — All alpha proteins
Fold Fold folda.93 — Heme-dependent peroxidases
Superfamily Superfamily superfamilya.93.1 — Heme-dependent peroxidases
Family Family familya.93.1.1 — CCP-like

CATH v4.4 (2 domains)

Domain ID domain_id1h5gA01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology520 — Peroxidase; domain 1
Homologous superfamily homologous superfamily10
Domain ID domain_id1h5gA02
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology420 — Peroxidase; domain 2
Homologous superfamily homologous superfamily10 — Peroxidase, domain 2

8. Citations (4)

9. Files and Curves (10)