9r9v

[FeFe]-hydrogenase from Nitratidesulfovibrio vulgaris str. Hildenborough at pH 7.00

Method: X-RAY DIFFRACTION Dmax: 67.5 Å Quality: GOOD

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

Periplasmic [Fe] hydrogenase small subunit

Nitratidesulfovibrio vulgaris str. Hildenborough

UniProt P07603

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 36–123 Not recorded Periplasmic [Fe] hydrogenase large subunit × 1 (P07598) IRON/SULFUR CLUSTER × 3 dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+) × 1 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 DI(HYDROXYETHYL)ETHER × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 1.25 Å R-free 0.153

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.

26 other PDB entries and 29 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PHFS_NITV2
Isoform
PDB entities 1
Chains and sequence ranges Author chain B; PDBConstruct 1–88; UniProt 36–123

Periplasmic [Fe] hydrogenase large subunit

Nitratidesulfovibrio vulgaris str. Hildenborough

UniProt P07598

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 2–395 Not recorded Periplasmic [Fe] hydrogenase small subunit × 1 (P07603) IRON/SULFUR CLUSTER × 3 dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+) × 1 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 DI(HYDROXYETHYL)ETHER × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 1.25 Å R-free 0.153

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.

26 other PDB entries and 29 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PHFL_NITV2
Isoform
PDB entities 2
Chains and sequence ranges Author chain A; PDBConstruct 1–394; UniProt 2–395

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 9r9v

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9r9v
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9r9v
Deposition date deposition_date2025-05-20
最后修订 last_revision2026-06-03
Structure title title[FeFe]-hydrogenase from Nitratidesulfovibrio vulgaris str. Hildenborough at pH 7.00
Keywords keywords[FeFe] hydrogenase, holo hydrogenase, iron-sulfur cluster, metalloenzyme, hydrogen production, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.78
Radius of gyration Rg (electron density) rg_electron20.96
Forward intensity I(0) i052093800.00
Molecular weight molecular_weight54770.0 kDa
Excluded volume excluded_volume67713 ų
Envelope volume envelope_volume74845 ų
Hydration-shell volume shell_volume28147 ų
Envelope diameter envelope_diameter70.4
Shell Rg shell_rg29.21
Envelope Rg envelope_rg21.45
Shape Rg shape_rg21.02
Total Rg total_rg21.66
Total atoms total_atoms7498
Residues n_residues482
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 dmax67.5
Rg (real space) rg_real21.63
Rg uncertainty (real space) rg_real_error0.27
I(0) (real space) i0_real5.2090e+07
I(0) uncertainty (real space) i0_real_error6.1110e+05
Rg (reciprocal space) rg_reciprocal21.66
I(0) (reciprocal space) i0_reciprocal52090000.0000
Solution quality estimate total_estimate0.8967
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.2
Skewness Skewness skewness0.168
Kurtosis Kurtosis kurtosis-0.452
Angular range angular_range— – 0.3650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16510000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.900; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.990; Smooth: 0.963

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)