5tzo

Computationally Designed Fentanyl Binder - Fen49*-Complex

Method: X-RAY DIFFRACTION Dmax: 79.4 Å Quality: EXCELLENT

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

Endo-1,4-beta-xylanase A

Bacillus subtilis (strain 168)

UniProt P18429

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 30–213 Fragment:UNP residues 30-213 7V7 N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide × 2 K POTASSIUM ION × 2 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;0.8M sodium phosphate, 0.8M potassium phosphate, 0.1M HEPES pH 7.5 Resolution 1.67 Å R-free 0.203
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 30–213 Fragment:UNP residues 30-213 7V7 N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide × 2 K POTASSIUM ION × 1 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;0.8M sodium phosphate, 0.8M potassium phosphate, 0.1M HEPES pH 7.5 Resolution 1.67 Å R-free 0.203
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 30–213 Fragment:UNP residues 30-213 7V7 N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide × 2 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;0.8M sodium phosphate, 0.8M potassium phosphate, 0.1M HEPES pH 7.5 Resolution 1.67 Å R-free 0.203

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 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name XYNA_BACSU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–188; UniProt 30–213 Author chain B; PDBConstruct 5–188; UniProt 30–213 Author chain C; PDBConstruct 5–188; UniProt 30–213

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 5tzo

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5tzo
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id5tzo
Deposition date deposition_date2016-11-22
Structure title titleComputationally Designed Fentanyl Binder - Fen49*-Complex
Keywords keywordsComputational Design, Fentanyl, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.46
Radius of gyration Rg (electron density) rg_electron25.38
Forward intensity I(0) i063507700.00
Molecular weight molecular_weight62047.0 kDa
Excluded volume excluded_volume77229 ų
Envelope volume envelope_volume88707 ų
Hydration-shell volume shell_volume29190 ų
Envelope diameter envelope_diameter81.9
Shell Rg shell_rg32.58
Envelope Rg envelope_rg25.29
Shape Rg shape_rg25.35
Total Rg total_rg26.24
Total atoms total_atoms8458
Residues n_residues555
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 dmax79.4
Rg (real space) rg_real26.36
Rg uncertainty (real space) rg_real_error0.52
I(0) (real space) i0_real6.3510e+07
I(0) uncertainty (real space) i0_real_error9.1910e+05
Rg (reciprocal space) rg_reciprocal26.39
I(0) (reciprocal space) i0_reciprocal63510000.0000
Solution quality estimate total_estimate0.9146
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.8
Skewness Skewness skewness0.152
Kurtosis Kurtosis kurtosis-0.667
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12700000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.972; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.976

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id5tzoA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain
Domain ID domain_id5tzoB00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain
Domain ID domain_id5tzoC00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain

8. Citations (1)

9. Files and Curves (10)