1c4c

BINDING OF EXOGENOUSLY ADDED CARBON MONOXIDE AT THE ACTIVE SITE OF THE FE-ONLY HYDROGENASE (CPI) FROM CLOSTRIDIUM PASTEURIANUM

Method: X-RAY DIFFRACTION Dmax: 83.4 Å Quality: GOOD

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

PROTEIN (FE-ONLY HYDROGENASE)

OrganismNot specified

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 1–574 Not recorded HC0 2 IRON/2 SULFUR/6 CARBONYL/1 WATER INORGANIC CLUSTER × 1 SF4 IRON/SULFUR CLUSTER × 4 FES FE2/S2 (INORGANIC) CLUSTER × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5;pH 5.0 Resolution 2.40 Å R-free 0.240

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 61 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 1–574; UniProt 1–574

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 1c4c

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1c4c
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1c4c
Deposition date deposition_date1999-08-16
Structure title titleBINDING OF EXOGENOUSLY ADDED CARBON MONOXIDE AT THE ACTIVE SITE OF THE FE-ONLY HYDROGENASE (CPI) FROM CLOSTRIDIUM PASTEURIANUM
Keywords keywordsMETALLOPROTEINS, [FES] CLUSTERS, HYDROGEN OXIDATION, PROTON REDUCTION, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.48
Radius of gyration Rg (electron density) rg_electron25.00
Forward intensity I(0) i077749000.00
Molecular weight molecular_weight65772.0 kDa
Excluded volume excluded_volume80753 ų
Envelope volume envelope_volume94955 ų
Hydration-shell volume shell_volume31298 ų
Envelope diameter envelope_diameter84.0
Shell Rg shell_rg32.73
Envelope Rg envelope_rg25.47
Shape Rg shape_rg25.14
Total Rg total_rg25.34
Total atoms total_atoms4514
Residues n_residues574
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 dmax83.4
Rg (real space) rg_real25.49
Rg uncertainty (real space) rg_real_error0.42
I(0) (real space) i0_real7.7750e+07
I(0) uncertainty (real space) i0_real_error1.0660e+06
Rg (reciprocal space) rg_reciprocal25.49
I(0) (reciprocal space) i0_reciprocal77750000.0000
Solution quality estimate total_estimate0.8853
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary28.3
Skewness Skewness skewness0.394
Kurtosis Kurtosis kurtosis-0.272
Angular range angular_range— – 0.3100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha27020000.0000
Real-space data points n_real_points63
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.858; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.936

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 5 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1c4ca1
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_idd1c4ca2
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.15.4.2 — 2Fe-2S ferredoxin domains from multidomain proteins
Domain ID domain_idd1c4ca3
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 (2 domains)

Domain ID domain_id1c4cA01
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily740
Domain ID domain_id1c4cA02
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)