2j18

Chloroperoxidase mixture of ferric and ferrous states (low dose data set)

Method: X-RAY DIFFRACTION Dmax: 61.2 Å Quality: GOOD

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

CHLOROPEROXIDASE

CALDARIOMYCES FUMAGO

UniProt P04963

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 Monomer Protein × 1 其他Polymer 3 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 22–319 Fragment:RESIDUES 22-319 Non-standard monomer:Yes (specific site not provided by mmCIF) alpha-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose × 1 MN MANGANESE (II) ION × 1 HEM PROTOPORPHYRIN IX CONTAINING FE × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 MAN alpha-D-mannopyranose × 9 BR BROMIDE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:pH 3.4;50MM KBR, 20% PEG3000, 0.1 M SODIUM CITRATE PH3.4, pH 3.40 Resolution 1.75 Å R-free 0.206

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 13 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PRXC_CALFU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–299; UniProt 22–319

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 2j18

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2j18
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2j18
Deposition date deposition_date2006-08-09
Structure title titleChloroperoxidase mixture of ferric and ferrous states (low dose data set)
Keywords keywordsOXIDOREDUCTASE, PYRROLIDONE CARBOXYLIC ACID, GLYCOPROTEIN, METAL-BINDING, IRON, HEME, CHLORIDE, MANGANESE, PEROXIDASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.75
Radius of gyration Rg (electron density) rg_electron18.52
Forward intensity I(0) i024030100.00
Molecular weight molecular_weight36591.0 kDa
Excluded volume excluded_volume45132 ų
Envelope volume envelope_volume49905 ų
Hydration-shell volume shell_volume21730 ų
Envelope diameter envelope_diameter64.3
Shell Rg shell_rg25.74
Envelope Rg envelope_rg18.92
Shape Rg shape_rg18.48
Total Rg total_rg19.55
Total atoms total_atoms2565
Residues n_residues298
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 dmax61.2
Rg (real space) rg_real19.59
Rg uncertainty (real space) rg_real_error0.30
I(0) (real space) i0_real2.4030e+07
I(0) uncertainty (real space) i0_real_error2.9850e+05
Rg (reciprocal space) rg_reciprocal19.61
I(0) (reciprocal space) i0_reciprocal24030000.0000
Solution quality estimate total_estimate0.8190
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary25.9
Skewness Skewness skewness0.100
Kurtosis Kurtosis kurtosis-0.452
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6354000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.887; Stabil: 0.997; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (10)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd2j18a1
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.3 — Cloroperoxidase
Family Family familya.39.3.1 — Cloroperoxidase
Domain ID domain_idd2j18a2
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.3 — Cloroperoxidase
Family Family familya.39.3.1 — Cloroperoxidase

CATH v4.4 (1 domains)

Domain ID domain_id2j18A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology489 — Chloroperoxidase
Homologous superfamily homologous superfamily10 — Chloroperoxidase-like

8. Citations (1)

9. Files and Curves (10)