3myt

Crystal structure of Ketosteroid Isomerase D38HD99N from Pseudomonas testosteroni (tKSI)

Method: X-RAY DIFFRACTION Dmax: 93.4 Å Quality: GOOD

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

Steroid Delta-isomerase

Comamonas testosteroni

UniProt P00947

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–125 Chain C; UniProt 1–125 Mutation:D38HD99N SO4 SULFATE ION × 6 EQU EQUILENIN × 2 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:sitting drop;pH 7.2;298 K;1.2 M ammonium sulfate, 40 mM potassium phosphate, 1 mM EDTA, 2mM DTT, 1.8mM equilenin, pH 7.2, sitting drop, temperature 298K Resolution 1.96 Å R-free 0.282
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 1–125 Chain D; UniProt 1–125 Mutation:D38HD99N SO4 SULFATE ION × 9 EQU EQUILENIN × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:sitting drop;pH 7.2;298 K;1.2 M ammonium sulfate, 40 mM potassium phosphate, 1 mM EDTA, 2mM DTT, 1.8mM equilenin, pH 7.2, sitting drop, temperature 298K Resolution 1.96 Å R-free 0.282
3 Protein homooligomer Homooligomer Protein × 8 PDB declaration: octameric(8) Consistent with protein copy count Chain A; UniProt 1–125 Chain B; UniProt 1–125 Chain C; UniProt 1–125 Chain D; UniProt 1–125 Mutation:D38HD99N SO4 SULFATE ION × 30 EQU EQUILENIN × 6 GOL GLYCEROL × 8 X-RAY DIFFRACTION X-ray crystallization conditions:sitting drop;pH 7.2;298 K;1.2 M ammonium sulfate, 40 mM potassium phosphate, 1 mM EDTA, 2mM DTT, 1.8mM equilenin, pH 7.2, sitting drop, temperature 298K Resolution 1.96 Å R-free 0.282
4 Protein homooligomer Homooligomer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–125 Chain B; UniProt 1–125 Chain C; UniProt 1–125 Chain D; UniProt 1–125 Mutation:D38HD99N SO4 SULFATE ION × 15 EQU EQUILENIN × 3 GOL GLYCEROL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:sitting drop;pH 7.2;298 K;1.2 M ammonium sulfate, 40 mM potassium phosphate, 1 mM EDTA, 2mM DTT, 1.8mM equilenin, pH 7.2, sitting drop, temperature 298K Resolution 1.96 Å R-free 0.282

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.

22 other PDB entries and 40 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SDIS_COMTE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–125; UniProt 1–125 Author chain B; PDBConstruct 1–125; UniProt 1–125 Author chain C; PDBConstruct 1–125; UniProt 1–125 Author chain D; PDBConstruct 1–125; UniProt 1–125

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 3myt

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3myt
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3myt
Deposition date deposition_date2010-05-11
Structure title titleCrystal structure of Ketosteroid Isomerase D38HD99N from Pseudomonas testosteroni (tKSI)
Keywords keywordsISOMERASE, lipid metabolism, steroid metabolism; ISOMERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.13
Radius of gyration Rg (electron density) rg_electron27.41
Forward intensity I(0) i055224100.00
Molecular weight molecular_weight56009.0 kDa
Excluded volume excluded_volume69310 ų
Envelope volume envelope_volume89563 ų
Hydration-shell volume shell_volume27794 ų
Envelope diameter envelope_diameter102.9
Shell Rg shell_rg33.99
Envelope Rg envelope_rg27.21
Shape Rg shape_rg27.40
Total Rg total_rg28.14
Total atoms total_atoms3929
Residues n_residues498
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 dmax93.4
Rg (real space) rg_real28.15
Rg uncertainty (real space) rg_real_error0.70
I(0) (real space) i0_real5.5220e+07
I(0) uncertainty (real space) i0_real_error8.5760e+05
Rg (reciprocal space) rg_reciprocal28.15
I(0) (reciprocal space) i0_reciprocal55220000.0000
Solution quality estimate total_estimate0.8933
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.4
Skewness Skewness skewness0.317
Kurtosis Kurtosis kurtosis-0.496
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha11950000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.887; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.951; Smooth: 0.997

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 8 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd3myta_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.17 — Cystatin-like
Superfamily Superfamily superfamilyd.17.4 — NTF2-like
Family Family familyd.17.4.3 — Ketosteroid isomerase-like
Domain ID domain_idd3mytb_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.17 — Cystatin-like
Superfamily Superfamily superfamilyd.17.4 — NTF2-like
Family Family familyd.17.4.3 — Ketosteroid isomerase-like
Domain ID domain_idd3mytc_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.17 — Cystatin-like
Superfamily Superfamily superfamilyd.17.4 — NTF2-like
Family Family familyd.17.4.3 — Ketosteroid isomerase-like
Domain ID domain_idd3mytd_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.17 — Cystatin-like
Superfamily Superfamily superfamilyd.17.4 — NTF2-like
Family Family familyd.17.4.3 — Ketosteroid isomerase-like

CATH v4.4 (4 domains)

Domain ID domain_id3mytA00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology450 — Nuclear Transport Factor 2; Chain: A,
Homologous superfamily homologous superfamily50
Domain ID domain_id3mytB00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology450 — Nuclear Transport Factor 2; Chain: A,
Homologous superfamily homologous superfamily50
Domain ID domain_id3mytC00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology450 — Nuclear Transport Factor 2; Chain: A,
Homologous superfamily homologous superfamily50
Domain ID domain_id3mytD00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology450 — Nuclear Transport Factor 2; Chain: A,
Homologous superfamily homologous superfamily50

8. Citations (1)

9. Files and Curves (10)