2fd2

CRYSTALLOGRAPHIC ANALYSIS OF TWO SITE-DIRECTED MUTANTS OF AZOTOBACTER VINELANDII FERREDOXIN

Method: X-RAY DIFFRACTION Dmax: 42.6 Å Quality: REASONABLE

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

FERREDOXIN

Azotobacter vinelandii

UniProt P00214

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 1–106 Not recorded SF4 IRON/SULFUR CLUSTER × 1 F3S FE3-S4 CLUSTER × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 1.90 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.

31 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FER1_AZOVI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–106; UniProt 1–106

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 2fd2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2fd2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2fd2
Deposition date deposition_date1990-08-20
Structure title titleCRYSTALLOGRAPHIC ANALYSIS OF TWO SITE-DIRECTED MUTANTS OF AZOTOBACTER VINELANDII FERREDOXIN
Keywords keywordsELECTRON TRANSFER(IRON-SULFUR PROTEIN); ELECTRON TRANSFER(IRON-SULFUR PROTEIN)
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier13.54
Radius of gyration Rg (electron density) rg_electron12.39
Forward intensity I(0) i03730590.00
Molecular weight molecular_weight12648.0 kDa
Excluded volume excluded_volume15253 ų
Envelope volume envelope_volume16073 ų
Hydration-shell volume shell_volume10878 ų
Envelope diameter envelope_diameter40.8
Shell Rg shell_rg18.40
Envelope Rg envelope_rg12.79
Shape Rg shape_rg12.50
Total Rg total_rg13.34
Total atoms total_atoms855
Residues n_residues106
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 dmax42.6
Rg (real space) rg_real13.45
Rg uncertainty (real space) rg_real_error0.17
I(0) (real space) i0_real3.7310e+06
I(0) uncertainty (real space) i0_real_error3.2760e+04
Rg (reciprocal space) rg_reciprocal13.46
I(0) (reciprocal space) i0_reciprocal3731000.0000
Solution quality estimate total_estimate0.7489
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary16.7
Skewness Skewness skewness0.127
Kurtosis Kurtosis kurtosis-0.395
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha504300.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.888; Stabil: 1.000; Sysdev: 0.368; Positv: 1.000; Valcen: 0.994; Smooth: 0.970

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2fd2a_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.58 — Ferredoxin-like
Superfamily Superfamily superfamilyd.58.1 — 4Fe-4S ferredoxins
Family Family familyd.58.1.2 — 7-Fe ferredoxin

CATH v4.4 (1 domains)

Domain ID domain_id2fd2A00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily20

8. Citations (12)

9. Files and Curves (10)