3a20

L122K mutant of FMN-binding protein from Desulfovibrio vulgaris (Miyazaki F)

Method: X-RAY DIFFRACTION Dmax: 65.1 Å Quality: REASONABLE

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

FMN-binding protein

;Desulfovibrio vulgaris str. 'Miyazaki F' ;

UniProt Q46604

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 1–122 Chain B; UniProt 1–122 Mutation:L122K FMN FLAVIN MONONUCLEOTIDE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;PEG 6000, sodium acetate, Tris, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K Resolution 1.60 Å R-free 0.188

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.

12 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FMNB_DESVM
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–122; UniProt 1–122 Author chain B; PDBConstruct 1–122; UniProt 1–122

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 3a20

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3a20
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3a20
Deposition date deposition_date2009-04-27
Structure title titleL122K mutant of FMN-binding protein from Desulfovibrio vulgaris (Miyazaki F)
Keywords keywordsBETA SHEET, Cytoplasm, Electron transport, Flavoprotein, FMN, Transport; ELECTRON TRANSPORT
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.40
Radius of gyration Rg (electron density) rg_electron17.23
Forward intensity I(0) i013446000.00
Molecular weight molecular_weight27223.0 kDa
Excluded volume excluded_volume34020 ų
Envelope volume envelope_volume38111 ų
Hydration-shell volume shell_volume18302 ų
Envelope diameter envelope_diameter62.0
Shell Rg shell_rg23.66
Envelope Rg envelope_rg17.47
Shape Rg shape_rg17.24
Total Rg total_rg18.15
Total atoms total_atoms1916
Residues n_residues244
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 dmax65.1
Rg (real space) rg_real18.29
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real1.3450e+07
I(0) uncertainty (real space) i0_real_error1.8790e+05
Rg (reciprocal space) rg_reciprocal18.31
I(0) (reciprocal space) i0_reciprocal13450000.0000
Solution quality estimate total_estimate0.6203
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.0
Skewness Skewness skewness0.188
Kurtosis Kurtosis kurtosis-0.237
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4381000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.633; Stabil: 0.997; Sysdev: 0.391; Positv: 1.000; Valcen: 0.999; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3a20a_
Class classb — All beta proteins
Fold Fold foldb.45 — Split barrel-like
Superfamily Superfamily superfamilyb.45.1 — FMN-binding split barrel
Family Family familyb.45.1.1 — PNP-oxidase like
Domain ID domain_idd3a20b_
Class classb — All beta proteins
Fold Fold foldb.45 — Split barrel-like
Superfamily Superfamily superfamilyb.45.1 — FMN-binding split barrel
Family Family familyb.45.1.1 — PNP-oxidase like

CATH v4.4 (2 domains)

Domain ID domain_id3a20A00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology110 — Pnp Oxidase; Chain A
Homologous superfamily homologous superfamily10 — Electron Transport, Fmn-binding Protein; Chain A
Domain ID domain_id3a20B00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology110 — Pnp Oxidase; Chain A
Homologous superfamily homologous superfamily10 — Electron Transport, Fmn-binding Protein; Chain A

8. Citations (1)

9. Files and Curves (10)