6gm0

[FeFe]-hydrogenase CpI from Clostridium pasteurianum, variant E279Q

Method: X-RAY DIFFRACTION Dmax: 103.8 Å Quality: GOOD

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

Iron hydrogenase 1

Clostridium pasteurianum

UniProt P29166

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 2–574 Mutation:E279Q 402 dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+) × 1 SF4 IRON/SULFUR CLUSTER × 4 FES FE2/S2 (INORGANIC) CLUSTER × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;20% PEG 4000, 0.4 M MgCl2,0.1 M MES, 20 % glycerol Resolution 2.11 Å R-free 0.228
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 2–574 Mutation:E279Q 402 dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+) × 1 SF4 IRON/SULFUR CLUSTER × 4 FES FE2/S2 (INORGANIC) CLUSTER × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;277 K;20% PEG 4000, 0.4 M MgCl2,0.1 M MES, 20 % glycerol Resolution 2.11 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.

35 other PDB entries and 60 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PHF1_CLOPA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–574; UniProt 2–574 Author chain B; PDBConstruct 2–574; UniProt 2–574

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 6gm0

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6gm0
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6gm0
Deposition date deposition_date2018-05-24
Structure title title[FeFe]-hydrogenase CpI from Clostridium pasteurianum, variant E279Q
Keywords keywordsHydrogenase, H-cluster, OXIDOREDUCTASE, semisynthetic enzyme; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.22
Radius of gyration Rg (electron density) rg_electron31.92
Forward intensity I(0) i0298850000.00
Molecular weight molecular_weight132030.0 kDa
Excluded volume excluded_volume162070 ų
Envelope volume envelope_volume198260 ų
Hydration-shell volume shell_volume50305 ų
Envelope diameter envelope_diameter107.8
Shell Rg shell_rg40.11
Envelope Rg envelope_rg31.76
Shape Rg shape_rg32.09
Total Rg total_rg31.96
Total atoms total_atoms9066
Residues n_residues1153
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 dmax103.8
Rg (real space) rg_real32.13
Rg uncertainty (real space) rg_real_error0.53
I(0) (real space) i0_real2.9890e+08
I(0) uncertainty (real space) i0_real_error4.0850e+06
Rg (reciprocal space) rg_reciprocal32.17
I(0) (reciprocal space) i0_reciprocal298900000.0000
Solution quality estimate total_estimate0.8881
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary38.1
Skewness Skewness skewness0.294
Kurtosis Kurtosis kurtosis-0.343
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha82970000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.895; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.857

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 12 domains

SCOP 2.08 (8 domains)

Domain ID domain_idd6gm0a1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.15 — beta-Grasp (ubiquitin-like)
Superfamily Superfamily superfamilyd.15.4 — 2Fe-2S ferredoxin-like
Family Family familyd.15.4.0 — automated matches
Domain ID domain_idd6gm0a2
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.58.1.0 — automated matches
Domain ID domain_idd6gm0a3
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.96 — Fe-only hydrogenase
Superfamily Superfamily superfamilyc.96.1 — Fe-only hydrogenase
Family Family familyc.96.1.1 — Fe-only hydrogenase
Domain ID domain_idd6gm0a4
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd6gm0b1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.15 — beta-Grasp (ubiquitin-like)
Superfamily Superfamily superfamilyd.15.4 — 2Fe-2S ferredoxin-like
Family Family familyd.15.4.0 — automated matches
Domain ID domain_idd6gm0b2
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.58.1.0 — automated matches
Domain ID domain_idd6gm0b3
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.96 — Fe-only hydrogenase
Superfamily Superfamily superfamilyc.96.1 — Fe-only hydrogenase
Family Family familyc.96.1.1 — Fe-only hydrogenase
Domain ID domain_idd6gm0b4
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (4 domains)

Domain ID domain_id6gm0A01
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily740
Domain ID domain_id6gm0A02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily20
Domain ID domain_id6gm0B01
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily740
Domain ID domain_id6gm0B02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily20

8. Citations (1)

9. Files and Curves (10)