5tvy

Computationally Designed Fentanyl Binder - Fen49

Method: X-RAY DIFFRACTION Dmax: 72.3 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 XPE 3,6,9,12,15,18,21,24,27-NONAOXANONACOSANE-1,29-DIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 3.5;293.15 K;1ul of protein at 20mg/ml mixed with 1ul of mother liquor, plus 0.2ul of a seed stock made from a previous crystallization drop. Crystallization condition is 0.1M Citric Acid pH 3.5, 25% PEG 3350. Resolution 1.00 Å R-free 0.121
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 XPE 3,6,9,12,15,18,21,24,27-NONAOXANONACOSANE-1,29-DIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 3.5;293.15 K;1ul of protein at 20mg/ml mixed with 1ul of mother liquor, plus 0.2ul of a seed stock made from a previous crystallization drop. Crystallization condition is 0.1M Citric Acid pH 3.5, 25% PEG 3350. Resolution 1.00 Å R-free 0.121

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 27 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

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 5tvy

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5tvy
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5tvy
Deposition date deposition_date2016-11-10
Structure title titleComputationally Designed Fentanyl Binder - Fen49
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_guinier23.15
Radius of gyration Rg (electron density) rg_electron22.35
Forward intensity I(0) i029989900.00
Molecular weight molecular_weight41464.0 kDa
Excluded volume excluded_volume51348 ų
Envelope volume envelope_volume58138 ų
Hydration-shell volume shell_volume22087 ų
Envelope diameter envelope_diameter73.5
Shell Rg shell_rg28.59
Envelope Rg envelope_rg22.25
Shape Rg shape_rg22.33
Total Rg total_rg23.13
Total atoms total_atoms5652
Residues n_residues375
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 dmax72.3
Rg (real space) rg_real23.15
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real2.9990e+07
I(0) uncertainty (real space) i0_real_error3.6000e+05
Rg (reciprocal space) rg_reciprocal23.15
I(0) (reciprocal space) i0_reciprocal29990000.0000
Solution quality estimate total_estimate0.9014
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.6
Skewness Skewness skewness0.316
Kurtosis Kurtosis kurtosis-0.541
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5880000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.909; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.993; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id5tvyA00
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_id5tvyB00
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)