8eno

Homocitrate-deficient nitrogenase MoFe-protein from A. vinelandii nifV knockout in complex with NafT

Method: ELECTRON MICROSCOPY Dmax: 133.8 Å Quality: GOOD

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

Nitrogenase molybdenum-iron protein alpha chain

OrganismNot specified

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain A; UniProt 4–480 Chain C; UniProt 4–480 Not recorded Nitrogenase molybdenum-iron protein beta chain × 2 (C1DGZ8) nitrogenase-associated factor T × 1 (C1DH13) ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 CIT CITRIC ACID × 1 CLF FE(8)-S(7) CLUSTER × 2 1N7 CHAPSO × 2 FE FE (III) ION × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.8 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 2.71 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.

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 1–477; UniProt 4–480 Author chain C; PDBConstruct 1–477; UniProt 4–480

Nitrogenase molybdenum-iron protein beta chain

OrganismNot specified

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain B; UniProt 2–523 Chain D; UniProt 2–523 Not recorded Nitrogenase molybdenum-iron protein alpha chain × 2 (P07328) nitrogenase-associated factor T × 1 (C1DH13) ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 CIT CITRIC ACID × 1 CLF FE(8)-S(7) CLUSTER × 2 1N7 CHAPSO × 2 FE FE (III) ION × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.8 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 2.71 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.

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 1–522; UniProt 2–523 Author chain D; PDBConstruct 1–522; UniProt 2–523

nitrogenase-associated factor T

OrganismNot specified

UniProt C1DH13

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain E; UniProt 1–132 Not recorded Nitrogenase molybdenum-iron protein alpha chain × 2 (P07328) Nitrogenase molybdenum-iron protein beta chain × 2 (C1DGZ8) ICS iron-sulfur-molybdenum cluster with interstitial carbon × 2 CIT CITRIC ACID × 1 CLF FE(8)-S(7) CLUSTER × 2 1N7 CHAPSO × 2 FE FE (III) ION × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.8 cryo-EM vitrification conditions:Cryogen ETHANE-PROPANE Resolution 2.71 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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name C1DH13_AZOVD
Isoform
PDB entities 3
Chains and sequence ranges Author chain E; PDBConstruct 1–132; UniProt 1–132

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 8eno

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8eno
Deposition date deposition_date2022-09-30
Structure title titleHomocitrate-deficient nitrogenase MoFe-protein from A. vinelandii nifV knockout in complex with NafT
Keywords keywordsnitrogenase, nitrogen fixation, reductase, MoFe, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier39.48
Radius of gyration Rg (electron density) rg_electron39.26
Forward intensity I(0) i0830505000.00
Molecular weight molecular_weight236440.0 kDa
Excluded volume excluded_volume294980 ų
Envelope volume envelope_volume343040 ų
Hydration-shell volume shell_volume70572 ų
Envelope diameter envelope_diameter142.7
Shell Rg shell_rg46.50
Envelope Rg envelope_rg39.59
Shape Rg shape_rg39.26
Total Rg total_rg39.59
Total atoms total_atoms16485
Residues n_residues2047
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 dmax133.8
Rg (real space) rg_real39.53
Rg uncertainty (real space) rg_real_error1.11
I(0) (real space) i0_real8.3050e+08
I(0) uncertainty (real space) i0_real_error1.3470e+07
Rg (reciprocal space) rg_reciprocal39.50
I(0) (reciprocal space) i0_reciprocal830500000.0000
Solution quality estimate total_estimate0.8626
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary43.5
Skewness Skewness skewness0.435
Kurtosis Kurtosis kurtosis-0.141
Angular range angular_range— – 0.2000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha243900000.0000
Real-space data points n_real_points41
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.813; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.994; Smooth: 0.776

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)