8e3t

Gallium-reconstituted nitrogenase MoFeP mutant S188A from Azotobacter vinelandii after IDS oxidation

Method: X-RAY DIFFRACTION Dmax: 123.2 Å Quality: GOOD

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

Nitrogenase molybdenum-iron protein alpha chain

Azotobacter vinelandii DJ

UniProt P07328

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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–492 Chain C; UniProt 1–492 Not recorded Nitrogenase molybdenum-iron protein beta chain × 2 (C1DGZ8) HCA 3-HYDROXY-3-CARBOXY-ADIPIC ACID × 2 ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 UFF FE(7)-S(7) CLUSTER × 2 FE FE (III) ION × 2 NA SODIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.5;293 K;20% PEG 8000, 100 mM Tris pH 8.5, 500 mM NaCl, 10 mM dithionite Resolution 2.20 Å R-free 0.243

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.

83 other PDB entries and 89 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NIFD_AZOVI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–492; UniProt 1–492 Author chain C; PDBConstruct 1–492; UniProt 1–492

Nitrogenase molybdenum-iron protein beta chain

Azotobacter vinelandii DJ

UniProt C1DGZ8

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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 1–523 Chain D; UniProt 1–523 Mutation:S188A Nitrogenase molybdenum-iron protein alpha chain × 2 (P07328) HCA 3-HYDROXY-3-CARBOXY-ADIPIC ACID × 2 ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 UFF FE(7)-S(7) CLUSTER × 2 FE FE (III) ION × 2 NA SODIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.5;293 K;20% PEG 8000, 100 mM Tris pH 8.5, 500 mM NaCl, 10 mM dithionite Resolution 2.20 Å R-free 0.243

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 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name C1DGZ8_AZOVD
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–523; UniProt 1–523 Author chain D; PDBConstruct 1–523; UniProt 1–523

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 8e3t

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8e3t
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8e3t
Deposition date deposition_date2022-08-17
Structure title titleGallium-reconstituted nitrogenase MoFeP mutant S188A from Azotobacter vinelandii after IDS oxidation
Keywords keywordsMoFeP, MoFe-protein, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.19
Radius of gyration Rg (electron density) rg_electron37.55
Forward intensity I(0) i0783141000.00
Molecular weight molecular_weight227070.0 kDa
Excluded volume excluded_volume282150 ų
Envelope volume envelope_volume324880 ų
Hydration-shell volume shell_volume68744 ų
Envelope diameter envelope_diameter123.4
Shell Rg shell_rg46.07
Envelope Rg envelope_rg37.59
Shape Rg shape_rg37.55
Total Rg total_rg37.94
Total atoms total_atoms31003
Residues n_residues1994
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 dmax123.2
Rg (real space) rg_real38.08
Rg uncertainty (real space) rg_real_error0.73
I(0) (real space) i0_real7.8310e+08
I(0) uncertainty (real space) i0_real_error1.1830e+07
Rg (reciprocal space) rg_reciprocal38.16
I(0) (reciprocal space) i0_reciprocal783200000.0000
Solution quality estimate total_estimate0.8966
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary42.1
Skewness Skewness skewness0.255
Kurtosis Kurtosis kurtosis-0.541
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha251800000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.902; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.948

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)