2c3y

CRYSTAL STRUCTURE OF THE RADICAL FORM OF PYRUVATE:FERREDOXIN OXIDOREDUCTASE FROM Desulfovibrio africanus

Method: X-RAY DIFFRACTION Dmax: 125.5 Å Quality: GOOD

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

PYRUVATE-FERREDOXIN OXIDOREDUCTASE

OrganismNot specified

UniProt P94692

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 2–1232 Chain B; UniProt 2–1232 Not recorded SF4 IRON/SULFUR CLUSTER × 6 HTL 2-ACETYL-THIAMINE DIPHOSPHATE × 2 MG MAGNESIUM ION × 2 CA CALCIUM ION × 2 CO2 CARBON DIOXIDE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 9;10% PEG6000, 100MM MGCL2, 100MM TRIS-HCL PH 9 Resolution 1.93 Å R-free 0.228

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.

10 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name P94692_DESAF
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1231; UniProt 2–1232 Author chain B; PDBConstruct 1–1231; UniProt 2–1232

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 2c3y

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2c3y
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2c3y
Deposition date deposition_date2005-10-13
Structure title titleCRYSTAL STRUCTURE OF THE RADICAL FORM OF PYRUVATE:FERREDOXIN OXIDOREDUCTASE FROM Desulfovibrio africanus
Keywords keywords;OXIDOREDUCTASE, 4FE-4S, IRON, IRON-SULFUR, IRON-SULFUR CLUSTER, PYRUVATE CATABOLISM, TPP-DEPENDENT ENZYME, METAL-BINDING, ELECTRON TRANSPORT ;; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.91
Radius of gyration Rg (electron density) rg_electron38.48
Forward intensity I(0) i01097890000.00
Molecular weight molecular_weight269210.0 kDa
Excluded volume excluded_volume335050 ų
Envelope volume envelope_volume399670 ų
Hydration-shell volume shell_volume80564 ų
Envelope diameter envelope_diameter134.3
Shell Rg shell_rg47.78
Envelope Rg envelope_rg39.09
Shape Rg shape_rg38.47
Total Rg total_rg38.97
Total atoms total_atoms18804
Residues n_residues2461
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 dmax125.5
Rg (real space) rg_real38.74
Rg uncertainty (real space) rg_real_error0.85
I(0) (real space) i0_real1.0980e+09
I(0) uncertainty (real space) i0_real_error1.8990e+07
Rg (reciprocal space) rg_reciprocal38.85
I(0) (reciprocal space) i0_reciprocal1098000000.0000
Solution quality estimate total_estimate0.8730
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks0
Primary peak position r_peak_primary
Skewness Skewness skewness0.292
Kurtosis Kurtosis kurtosis-0.250
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha301100000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.852; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.982; Smooth: 0.807

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

7. Fold Classification (SCOP + CATH) 24 domains

SCOP 2.08 (10 domains)

Domain ID domain_idd2c3ya1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.36 — Thiamin diphosphate-binding fold (THDP-binding)
Superfamily Superfamily superfamilyc.36.1 — Thiamin diphosphate-binding fold (THDP-binding)
Family Family familyc.36.1.8 — PFOR Pyr module
Domain ID domain_idd2c3ya2
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.36 — Thiamin diphosphate-binding fold (THDP-binding)
Superfamily Superfamily superfamilyc.36.1 — Thiamin diphosphate-binding fold (THDP-binding)
Family Family familyc.36.1.12 — PFOR PP module
Domain ID domain_idd2c3ya3
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.48 — TK C-terminal domain-like
Superfamily Superfamily superfamilyc.48.1 — TK C-terminal domain-like
Family Family familyc.48.1.3 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain II
Domain ID domain_idd2c3ya4
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.64 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Superfamily Superfamily superfamilyc.64.1 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Family Family familyc.64.1.1 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Domain ID domain_idd2c3ya5
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.58.1.5 — Ferredoxin domains from multidomain proteins
Domain ID domain_idd2c3yb1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.36 — Thiamin diphosphate-binding fold (THDP-binding)
Superfamily Superfamily superfamilyc.36.1 — Thiamin diphosphate-binding fold (THDP-binding)
Family Family familyc.36.1.8 — PFOR Pyr module
Domain ID domain_idd2c3yb2
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.36 — Thiamin diphosphate-binding fold (THDP-binding)
Superfamily Superfamily superfamilyc.36.1 — Thiamin diphosphate-binding fold (THDP-binding)
Family Family familyc.36.1.12 — PFOR PP module
Domain ID domain_idd2c3yb3
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.48 — TK C-terminal domain-like
Superfamily Superfamily superfamilyc.48.1 — TK C-terminal domain-like
Family Family familyc.48.1.3 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain II
Domain ID domain_idd2c3yb4
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.64 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Superfamily Superfamily superfamilyc.64.1 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Family Family familyc.64.1.1 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Domain ID domain_idd2c3yb5
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.58.1.5 — Ferredoxin domains from multidomain proteins

CATH v4.4 (14 domains)

Domain ID domain_id2c3yA01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily970 — Thiamin diphosphate (ThDP)-binding fold, Pyr/PP domains
Domain ID domain_id2c3yA02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily920
Domain ID domain_id2c3yA03
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology920 — Pyruvate-ferredoxin Oxidoreductase; domain 3
Homologous superfamily homologous superfamily10 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Domain ID domain_id2c3yA04
Class class4 — Few Secondary Structures
Architecture architecture10 — Irregular
Topology topology780 — Pyruvate-ferredoxin Oxidoreductase; domain 4
Homologous superfamily homologous superfamily10 — Pyruvate-flavodoxin oxidoreductase, EKR domain
Domain ID domain_id2c3yA05
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily20
Domain ID domain_id2c3yA06
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily970 — Thiamin diphosphate (ThDP)-binding fold, Pyr/PP domains
Domain ID domain_id2c3yA07
Class class4 — Few Secondary Structures
Architecture architecture10 — Irregular
Topology topology790 — Pyruvate-ferredoxin Oxidoreductase; domain 7
Homologous superfamily homologous superfamily10 — Pyruvate-ferredoxin Oxidoreductase; domain 7
Domain ID domain_id2c3yB01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily970 — Thiamin diphosphate (ThDP)-binding fold, Pyr/PP domains
Domain ID domain_id2c3yB02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily920
Domain ID domain_id2c3yB03
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology920 — Pyruvate-ferredoxin Oxidoreductase; domain 3
Homologous superfamily homologous superfamily10 — Pyruvate-ferredoxin oxidoreductase, PFOR, domain III
Domain ID domain_id2c3yB04
Class class4 — Few Secondary Structures
Architecture architecture10 — Irregular
Topology topology780 — Pyruvate-ferredoxin Oxidoreductase; domain 4
Homologous superfamily homologous superfamily10 — Pyruvate-flavodoxin oxidoreductase, EKR domain
Domain ID domain_id2c3yB05
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily20
Domain ID domain_id2c3yB06
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily970 — Thiamin diphosphate (ThDP)-binding fold, Pyr/PP domains
Domain ID domain_id2c3yB07
Class class4 — Few Secondary Structures
Architecture architecture10 — Irregular
Topology topology790 — Pyruvate-ferredoxin Oxidoreductase; domain 7
Homologous superfamily homologous superfamily10 — Pyruvate-ferredoxin Oxidoreductase; domain 7

8. Citations (2)

9. Files and Curves (10)