8vbs

E. coli cysteine desulfurase SufS bound to SufE C51A

Method: X-RAY DIFFRACTION Dmax: 109.4 Å Quality: GOOD

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

Cysteine desulfurase

Escherichia coli

UniProt P77444

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–406 Chain B; UniProt 1–406 Non-standard monomer:Yes (specific site not provided by mmCIF) Cysteine desulfuration protein SufE × 2 (J7Q7S7) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;24.5-31.5% w/v PEG2000 MME, 0.1 M KSCN Resolution 3.31 Å R-free 0.272

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.

16 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SUFS_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–406; UniProt 1–406 Author chain B; PDBConstruct 1–406; UniProt 1–406

Cysteine desulfuration protein SufE

Escherichia coli

UniProt J7Q7S7

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 1–138 Chain D; UniProt 1–138 Mutation:C51A, E107C Cysteine desulfurase × 2 (P77444) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;24.5-31.5% w/v PEG2000 MME, 0.1 M KSCN Resolution 3.31 Å R-free 0.272

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name J7Q7S7_ECOLX
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–138; UniProt 1–138 Author chain D; PDBConstruct 1–138; UniProt 1–138

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 8vbs

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8vbs
Deposition date deposition_date2023-12-12
Structure title titleE. coli cysteine desulfurase SufS bound to SufE C51A
Keywords keywords;pyridoxal 5'-phosphate, cysteine desulfurase, transpersulfurase, iron-sulfur cluster, persulfide, TRANSFERASE ;; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.20
Radius of gyration Rg (electron density) rg_electron31.57
Forward intensity I(0) i0220607000.00
Molecular weight molecular_weight119030.0 kDa
Excluded volume excluded_volume149050 ų
Envelope volume envelope_volume184100 ų
Hydration-shell volume shell_volume47572 ų
Envelope diameter envelope_diameter117.5
Shell Rg shell_rg39.43
Envelope Rg envelope_rg31.97
Shape Rg shape_rg31.56
Total Rg total_rg32.21
Total atoms total_atoms8374
Residues n_residues1067
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 dmax109.4
Rg (real space) rg_real32.17
Rg uncertainty (real space) rg_real_error0.83
I(0) (real space) i0_real2.2060e+08
I(0) uncertainty (real space) i0_real_error3.5660e+06
Rg (reciprocal space) rg_reciprocal32.18
I(0) (reciprocal space) i0_reciprocal220600000.0000
Solution quality estimate total_estimate0.8700
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary38.0
Skewness Skewness skewness0.379
Kurtosis Kurtosis kurtosis-0.151
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha160500000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.798; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.916

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)