1akr

G61A OXIDIZED FLAVODOXIN MUTANT

Method: X-RAY DIFFRACTION Dmax: 48.3 Å Quality: GOOD

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

FLAVODOXIN

Desulfovibrio vulgaris subsp. vulgaris str. Hildenborough

UniProt P00323

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 2–148 Mutation:G61A FMN FLAVIN MONONUCLEOTIDE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;60-70% AMMONIUM SULFATE, 100MM TRIS-HCL, pH 7.0 Resolution 1.58 Å

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.

39 other PDB entries and 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FLAV_DESVH
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–147; UniProt 2–148

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 1akr

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1akr
Deposition date deposition_date1997-05-27
Structure title titleG61A OXIDIZED FLAVODOXIN MUTANT
Keywords keywordsELECTRON TRANSPORT, ELECTRON TRANSFER, FLAVOPROTEIN, FMN, FLAVODOXIN, MUTANT; ELECTRON TRANSPORT
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.58
Radius of gyration Rg (electron density) rg_electron14.08
Forward intensity I(0) i05526500.00
Molecular weight molecular_weight16143.0 kDa
Excluded volume excluded_volume19795 ų
Envelope volume envelope_volume21982 ų
Hydration-shell volume shell_volume13092 ų
Envelope diameter envelope_diameter47.6
Shell Rg shell_rg20.11
Envelope Rg envelope_rg14.36
Shape Rg shape_rg14.11
Total Rg total_rg15.13
Total atoms total_atoms1136
Residues n_residues147
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 dmax48.3
Rg (real space) rg_real15.46
Rg uncertainty (real space) rg_real_error0.25
I(0) (real space) i0_real5.5270e+06
I(0) uncertainty (real space) i0_real_error5.7670e+04
Rg (reciprocal space) rg_reciprocal15.48
I(0) (reciprocal space) i0_reciprocal5527000.0000
Solution quality estimate total_estimate0.8953
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.8
Skewness Skewness skewness0.077
Kurtosis Kurtosis kurtosis-0.415
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha960000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.892; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.988; Smooth: 0.973

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1akra_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.5 — Flavoproteins
Family Family familyc.23.5.1 — Flavodoxin-related

CATH v4.4 (1 domains)

Domain ID domain_id1akrA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily360 — Flavodoxin domain

8. Citations (6)

9. Files and Curves (10)