5b0u

Crystal structure of the mutated 19 kDa protein of Oplophorus luciferase (nanoKAZ)

Method: X-RAY DIFFRACTION Dmax: 110.1 Å Quality: REASONABLE

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

Oplophorus-luciferin 2-monooxygenase catalytic subunit

Oplophorus gracilirostris

UniProt Q9GV45

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 28–196 Mutation:A4E, Q11R, Q18L, L27V, A33N, K43R, V44I, A54I, F68D, L72Q, M75K,I90V, P115E, Q124K, Y138I, N166R No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;1.1 M di-ammonium tartrate Resolution 1.71 Å R-free 0.226
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 28–196 Mutation:A4E, Q11R, Q18L, L27V, A33N, K43R, V44I, A54I, F68D, L72Q, M75K,I90V, P115E, Q124K, Y138I, N166R No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;1.1 M di-ammonium tartrate Resolution 1.71 Å R-free 0.226

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.

21 other PDB entries and 44 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LUCI_OPLGR
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 23–191; UniProt 28–196 Author chain B; PDBConstruct 23–191; UniProt 28–196

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 5b0u

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5b0u
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id5b0u
Deposition date deposition_date2015-11-04
Structure title titleCrystal structure of the mutated 19 kDa protein of Oplophorus luciferase (nanoKAZ)
Keywords keywordsOplophorus luciferase, LUMINESCENT PROTEIN; LUMINESCENT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier35.24
Radius of gyration Rg (electron density) rg_electron34.84
Forward intensity I(0) i020876600.00
Molecular weight molecular_weight37979.0 kDa
Excluded volume excluded_volume48181 ų
Envelope volume envelope_volume70234 ų
Hydration-shell volume shell_volume16715 ų
Envelope diameter envelope_diameter103.6
Shell Rg shell_rg42.06
Envelope Rg envelope_rg33.03
Shape Rg shape_rg34.84
Total Rg total_rg35.46
Total atoms total_atoms2688
Residues n_residues338
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 dmax110.1
Rg (real space) rg_real35.52
Rg uncertainty (real space) rg_real_error1.12
I(0) (real space) i0_real2.0880e+07
I(0) uncertainty (real space) i0_real_error3.5790e+05
Rg (reciprocal space) rg_reciprocal35.36
I(0) (reciprocal space) i0_reciprocal20870000.0000
Solution quality estimate total_estimate0.6337
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary22.0
Skewness Skewness skewness0.158
Kurtosis Kurtosis kurtosis-1.352
Angular range angular_range— – 0.2250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3361000.0000
Real-space data points n_real_points46
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.030; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.156; Smooth: 0.989

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)