1g2a

THE CRYSTAL STRUCTURE OF E.COLI PEPTIDE DEFORMYLASE COMPLEXED WITH ACTINONIN

Method: X-RAY DIFFRACTION Dmax: 92.8 Å Quality: GOOD

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

POLYPEPTIDE DEFORMYLASE

Escherichia coli

UniProt P0A6K3

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 1–168 Not recorded NI NICKEL (II) ION × 1 BB2 ACTINONIN × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;290 K;10mg/ml PDF, 20mM actinonin, 50mM HEPES, pH 7.5 + 25-32% PEG 4000, 0.1M sodium citrate, pH 5.6, 0.2M ammonium acetate, VAPOR DIFFUSION, HANGING DROP at 290K Resolution 1.75 Å R-free 0.250
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1–168 Not recorded NI NICKEL (II) ION × 1 BB2 ACTINONIN × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;290 K;10mg/ml PDF, 20mM actinonin, 50mM HEPES, pH 7.5 + 25-32% PEG 4000, 0.1M sodium citrate, pH 5.6, 0.2M ammonium acetate, VAPOR DIFFUSION, HANGING DROP at 290K Resolution 1.75 Å R-free 0.250
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 1–168 Not recorded NI NICKEL (II) ION × 1 BB2 ACTINONIN × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;290 K;10mg/ml PDF, 20mM actinonin, 50mM HEPES, pH 7.5 + 25-32% PEG 4000, 0.1M sodium citrate, pH 5.6, 0.2M ammonium acetate, VAPOR DIFFUSION, HANGING DROP at 290K Resolution 1.75 Å R-free 0.250

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.

30 other PDB entries and 53 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DEF_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–168; UniProt 1–168 Author chain B; PDBConstruct 1–168; UniProt 1–168 Author chain C; PDBConstruct 1–168; UniProt 1–168

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 1g2a

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1g2a
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1g2a
Deposition date deposition_date2000-10-18
Structure title titleTHE CRYSTAL STRUCTURE OF E.COLI PEPTIDE DEFORMYLASE COMPLEXED WITH ACTINONIN
Keywords keywordsactinonin, inhibition, Polypeptide deformylase, hydrolase; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.35
Radius of gyration Rg (electron density) rg_electron27.80
Forward intensity I(0) i053870800.00
Molecular weight molecular_weight57567.0 kDa
Excluded volume excluded_volume72420 ų
Envelope volume envelope_volume92997 ų
Hydration-shell volume shell_volume28454 ų
Envelope diameter envelope_diameter94.7
Shell Rg shell_rg34.28
Envelope Rg envelope_rg27.58
Shape Rg shape_rg27.80
Total Rg total_rg28.47
Total atoms total_atoms4029
Residues n_residues492
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 dmax92.8
Rg (real space) rg_real28.38
Rg uncertainty (real space) rg_real_error0.68
I(0) (real space) i0_real5.3870e+07
I(0) uncertainty (real space) i0_real_error8.0840e+05
Rg (reciprocal space) rg_reciprocal28.37
I(0) (reciprocal space) i0_reciprocal53870000.0000
Solution quality estimate total_estimate0.8920
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary33.1
Skewness Skewness skewness0.321
Kurtosis Kurtosis kurtosis-0.411
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10850000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.917; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.957; Smooth: 0.884

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1g2aa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.167 — Peptide deformylase
Superfamily Superfamily superfamilyd.167.1 — Peptide deformylase
Family Family familyd.167.1.1 — Peptide deformylase
Domain ID domain_idd1g2ab_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.167 — Peptide deformylase
Superfamily Superfamily superfamilyd.167.1 — Peptide deformylase
Family Family familyd.167.1.1 — Peptide deformylase
Domain ID domain_idd1g2ac_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.167 — Peptide deformylase
Superfamily Superfamily superfamilyd.167.1 — Peptide deformylase
Family Family familyd.167.1.1 — Peptide deformylase

CATH v4.4 (3 domains)

Domain ID domain_id1g2aA00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology45 — Peptide Deformylase
Homologous superfamily homologous superfamily10 — Peptide deformylase
Domain ID domain_id1g2aB00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology45 — Peptide Deformylase
Homologous superfamily homologous superfamily10 — Peptide deformylase
Domain ID domain_id1g2aC00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology45 — Peptide Deformylase
Homologous superfamily homologous superfamily10 — Peptide deformylase

8. Citations (1)

9. Files and Curves (10)