1jf9

Crystal Structure of selenocysteine lyase

Method: X-RAY DIFFRACTION Dmax: 80.2 Å Quality: GOOD

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

SELENOCYSTEINE LYASE

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–406 Not recorded PLP PYRIDOXAL-5'-PHOSPHATE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291 K;4M NACL, VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 2.00 Å R-free 0.207

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 3–408; UniProt 1–406

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 1jf9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1jf9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1jf9
Deposition date deposition_date2001-06-20
Structure title titleCrystal Structure of selenocysteine lyase
Keywords keywords;NIFS, SELENOCYSTEINE, CYSTEINE, PURSULFIDE, Structural Genomics, PSI, Protein Structure Initiative, New York SGX Research Center for Structural Genomics, NYSGXRC, LYASE ;; LYASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.16
Radius of gyration Rg (electron density) rg_electron22.14
Forward intensity I(0) i033636300.00
Molecular weight molecular_weight44523.0 kDa
Excluded volume excluded_volume55618 ų
Envelope volume envelope_volume64774 ų
Hydration-shell volume shell_volume24325 ų
Envelope diameter envelope_diameter82.5
Shell Rg shell_rg29.07
Envelope Rg envelope_rg22.60
Shape Rg shape_rg22.16
Total Rg total_rg22.92
Total atoms total_atoms3134
Residues n_residues405
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 dmax80.2
Rg (real space) rg_real23.11
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real3.3640e+07
I(0) uncertainty (real space) i0_real_error4.6970e+05
Rg (reciprocal space) rg_reciprocal23.12
I(0) (reciprocal space) i0_reciprocal33640000.0000
Solution quality estimate total_estimate0.8663
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.1
Skewness Skewness skewness0.306
Kurtosis Kurtosis kurtosis-0.326
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7913000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.775; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.983; Smooth: 0.949

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1jf9a_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.67 — PLP-dependent transferase-like
Superfamily Superfamily superfamilyc.67.1 — PLP-dependent transferases
Family Family familyc.67.1.3 — Cystathionine synthase-like

CATH v4.4 (2 domains)

Domain ID domain_id1jf9A01
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily10 — Aspartate Aminotransferase, domain 1
Domain ID domain_id1jf9A02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology640 — Aspartate Aminotransferase; domain 2
Homologous superfamily homologous superfamily10 — Type I PLP-dependent aspartate aminotransferase-like (Major domain)

8. Citations (1)

9. Files and Curves (10)