1ye9

Crystal structure of proteolytically truncated catalase HPII from E. coli

Method: X-RAY DIFFRACTION Dmax: 187.8 Å Quality: REASONABLE

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

catalase HPII

Escherichia coli

UniProt P21179

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 homooligomer Homooligomer Protein × 8 PDB declaration: octameric(8) Consistent with protein copy count Chain A; UniProt 75–300 Chain B; UniProt 75–300 Chain C; UniProt 75–300 Chain D; UniProt 75–300 Chain E; UniProt 309–567 Chain F; UniProt 309–567 Chain G; UniProt 309–567 Chain H; UniProt 309–567 Fragment:proteolytic fragment, residues 75-300 Fragment:proteolytic fragment, residues 309-567 HDD CIS-HEME D HYDROXYCHLORIN GAMMA-SPIROLACTONE × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;298 K;50mM TrisHCl, 8% PEG 20000, 8% PEG MME 550, 0.2M KSCN, 0.1M dithiothreitol, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 2.80 Å R-free 0.269
2 Protein homooligomer Homooligomer Protein × 8 PDB declaration: octameric(8) Consistent with protein copy count Chain I; UniProt 75–300 Chain J; UniProt 75–300 Chain K; UniProt 75–300 Chain L; UniProt 75–300 Chain M; UniProt 309–567 Chain N; UniProt 309–567 Chain O; UniProt 309–567 Chain P; UniProt 309–567 Fragment:proteolytic fragment, residues 75-300 Fragment:proteolytic fragment, residues 309-567 HDD CIS-HEME D HYDROXYCHLORIN GAMMA-SPIROLACTONE × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;298 K;50mM TrisHCl, 8% PEG 20000, 8% PEG MME 550, 0.2M KSCN, 0.1M dithiothreitol, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 2.80 Å R-free 0.269

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.

46 other PDB entries and 47 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CATE_ECOLI
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–226; UniProt 75–300 Author chain B; PDBConstruct 1–226; UniProt 75–300 Author chain C; PDBConstruct 1–226; UniProt 75–300 Author chain D; PDBConstruct 1–226; UniProt 75–300 Author chain I; PDBConstruct 1–226; UniProt 75–300 Author chain J; PDBConstruct 1–226; UniProt 75–300 Author chain K; PDBConstruct 1–226; UniProt 75–300 Author chain L; PDBConstruct 1–226; UniProt 75–300 Author chain E; PDBConstruct 1–259; UniProt 309–567 Author chain F; PDBConstruct 1–259; UniProt 309–567 Author chain G; PDBConstruct 1–259; UniProt 309–567 Author chain H; PDBConstruct 1–259; UniProt 309–567 Author chain M; PDBConstruct 1–259; UniProt 309–567 Author chain N; PDBConstruct 1–259; UniProt 309–567 Author chain O; PDBConstruct 1–259; UniProt 309–567 Author chain P; PDBConstruct 1–259; UniProt 309–567

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 1ye9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1ye9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1ye9
Deposition date deposition_date2004-12-28
Structure title titleCrystal structure of proteolytically truncated catalase HPII from E. coli
Keywords keywordscatalase HPII, proteolytic truncation, beta barrel core, Oxidoreductase; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier63.72
Radius of gyration Rg (electron density) rg_electron64.36
Forward intensity I(0) i02757220000.00
Molecular weight molecular_weight443630.0 kDa
Excluded volume excluded_volume552920 ų
Envelope volume envelope_volume716550 ų
Hydration-shell volume shell_volume89422 ų
Envelope diameter envelope_diameter205.2
Shell Rg shell_rg69.47
Envelope Rg envelope_rg62.85
Shape Rg shape_rg64.35
Total Rg total_rg64.48
Total atoms total_atoms31472
Residues n_residues3832
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 dmax187.8
Rg (real space) rg_real64.25
Rg uncertainty (real space) rg_real_error1.52
I(0) (real space) i0_real2.7570e+09
I(0) uncertainty (real space) i0_real_error5.8820e+07
Rg (reciprocal space) rg_reciprocal63.14
I(0) (reciprocal space) i0_reciprocal2752000000.0000
Solution quality estimate total_estimate0.7475
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary45.1
Skewness Skewness skewness0.309
Kurtosis Kurtosis kurtosis-0.975
Angular range angular_range— – 0.1250 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha462800000.0000
Real-space data points n_real_points26
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.628; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.830; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 24 domains

CATH v4.4 (24 domains)

Domain ID domain_id1ye9A01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9A02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9A03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9B01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9B02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9B03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9C01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9C02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9C03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9D01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9D02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9D03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9I01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9I02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9I03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9J01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9J02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9J03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9K01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9K02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9K03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain
Domain ID domain_id1ye9L01
Class class6 — Special
Architecture architecture10 — Helix non-globular
Topology topology10 — Helicase, Ruva Protein; domain 3
Homologous superfamily homologous superfamily30 — Catalase hpii, N-terminal domain-like
Domain ID domain_id1ye9L02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology470 — catalase hpii fold
Homologous superfamily homologous superfamily10 — catalase hpii domain
Domain ID domain_id1ye9L03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily1060 — Catalase HPII, helical domain

8. Citations (1)

9. Files and Curves (10)