7tpv

Selenium-free nitrogenase Fe protein (Av2) from A. vinelandii (5mM KSeCN Soaked)

Method: X-RAY DIFFRACTION Dmax: 64.8 Å Quality: GOOD

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

Nitrogenase iron protein 1

OrganismNot specified

UniProt P00459

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 1–290 Not recorded ADP ADENOSINE-5'-DIPHOSPHATE × 2 SF4 IRON/SULFUR CLUSTER × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;36-41% PEG400, 0.1-0.3 M sodium chloride, 0.1 M HEPES, pH 7.5, 2.5 mM dithionite, 0.17 mM Cymal-7, 5 mM potassium selenocyanate Resolution 1.49 Å R-free 0.199

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.

47 other PDB entries and 52 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NIFH1_AZOVI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–290; UniProt 1–290

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 7tpv

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7tpv
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id7tpv
Deposition date deposition_date2022-01-26
Structure title titleSelenium-free nitrogenase Fe protein (Av2) from A. vinelandii (5mM KSeCN Soaked)
Keywords keywordsnitrogenase, metalloprotein, iron sulfur cluster, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.33
Radius of gyration Rg (electron density) rg_electron18.18
Forward intensity I(0) i017621700.00
Molecular weight molecular_weight30724.0 kDa
Excluded volume excluded_volume38004 ų
Envelope volume envelope_volume42952 ų
Hydration-shell volume shell_volume19499 ų
Envelope diameter envelope_diameter65.1
Shell Rg shell_rg24.88
Envelope Rg envelope_rg18.62
Shape Rg shape_rg18.18
Total Rg total_rg19.08
Total atoms total_atoms2142
Residues n_residues277
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 dmax64.8
Rg (real space) rg_real19.23
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real1.7620e+07
I(0) uncertainty (real space) i0_real_error1.9870e+05
Rg (reciprocal space) rg_reciprocal19.25
I(0) (reciprocal space) i0_reciprocal17620000.0000
Solution quality estimate total_estimate0.8740
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.7
Skewness Skewness skewness0.246
Kurtosis Kurtosis kurtosis-0.258
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4343000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.794; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.979

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)