9hb9

A. vinelandii nitrogenase MoFe protein Anc1a

Method: X-RAY DIFFRACTION Dmax: 124.4 Å Quality: GOOD

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

Nitrogenase molybdenum-iron protein beta chain

OrganismNot specified

UniProt P07329

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 Not recorded MoFe nitrogenase subunit D × 2 ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 HCA 3-HYDROXY-3-CARBOXY-ADIPIC ACID × 2 CLF FE(8)-S(7) CLUSTER × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.2 M LiSO4 x 1 H2O, 0.1 M bis-Tris/HCl at pH 6.5, 25%(w/v) of polyethylene glycol 3350 Resolution 2.66 Å R-free 0.220

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.

74 other PDB entries and 81 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NIFK_AZOVI
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 9hb9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9hb9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9hb9
Deposition date deposition_date2024-11-05
Structure title titleA. vinelandii nitrogenase MoFe protein Anc1a
Keywords keywordsNitrogen fixation, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.38
Radius of gyration Rg (electron density) rg_electron37.70
Forward intensity I(0) i0802988000.00
Molecular weight molecular_weight229950.0 kDa
Excluded volume excluded_volume285870 ų
Envelope volume envelope_volume329460 ų
Hydration-shell volume shell_volume69448 ų
Envelope diameter envelope_diameter125.2
Shell Rg shell_rg46.07
Envelope Rg envelope_rg37.72
Shape Rg shape_rg37.71
Total Rg total_rg38.09
Total atoms total_atoms16038
Residues n_residues1998
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 dmax124.4
Rg (real space) rg_real38.27
Rg uncertainty (real space) rg_real_error0.73
I(0) (real space) i0_real8.0300e+08
I(0) uncertainty (real space) i0_real_error1.2720e+07
Rg (reciprocal space) rg_reciprocal38.34
I(0) (reciprocal space) i0_reciprocal803000000.0000
Solution quality estimate total_estimate0.8960
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary42.5
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_alpha268400000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.897; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.956

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (2)

9. Files and Curves (10)