1lws

Crystal structure of the intein homing endonuclease PI-SceI bound to its recognition sequence

Method: X-RAY DIFFRACTION Dmax: 104.6 Å Quality: REASONABLE

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

ENDONUCLEASE PI-SCEI

Saccharomyces cerevisiae

UniProt P17255

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–DNA Monomer Protein × 1 DNA 2 PDB declaration: trimeric(3) Consistent with all polymer counts Chain A; UniProt 284–737 Non-standard monomer:Yes (specific site not provided by mmCIF) PI-SceI DNA recognition region top strand × 1 PI-SceI DNA recognition region bottom strand × 1 CA CALCIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;291 K;PEG 200, na hepes, calcium chloride, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 3.50 Å R-free 0.310

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.

15 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VATA_YEAST
Isoform
PDB entities 3
Chains and sequence ranges Author chain A; PDBConstruct 1–454; UniProt 284–737

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 1lws

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1lws
Deposition date deposition_date2002-06-03
Structure title titleCrystal structure of the intein homing endonuclease PI-SceI bound to its recognition sequence
Keywords keywordshoming endonuclease, intein, protein-DNA complex, endonuclease, HYDROLASE-DNA COMPLEX; HYDROLASE/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.89
Radius of gyration Rg (electron density) rg_electron28.67
Forward intensity I(0) i0111253000.00
Molecular weight molecular_weight69281.0 kDa
Excluded volume excluded_volume80446 ų
Envelope volume envelope_volume105740 ų
Hydration-shell volume shell_volume31870 ų
Envelope diameter envelope_diameter110.2
Shell Rg shell_rg34.51
Envelope Rg envelope_rg28.96
Shape Rg shape_rg28.59
Total Rg total_rg29.32
Total atoms total_atoms4756
Residues n_residues487
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 dmax104.6
Rg (real space) rg_real30.03
Rg uncertainty (real space) rg_real_error1.07
I(0) (real space) i0_real1.1130e+08
I(0) uncertainty (real space) i0_real_error1.7800e+06
Rg (reciprocal space) rg_reciprocal29.97
I(0) (reciprocal space) i0_reciprocal111200000.0000
Solution quality estimate total_estimate0.6623
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary33.6
Skewness Skewness skewness0.505
Kurtosis Kurtosis kurtosis-0.065
Angular range angular_range— – 0.2650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha9291000.0000
Real-space data points n_real_points54
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.792; Stabil: 1.000; Sysdev: 0.135; Positv: 1.000; Valcen: 0.910; Smooth: 0.915

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1lwsa1
Class classb — All beta proteins
Fold Fold foldb.86 — Hedgehog/intein (Hint) domain
Superfamily Superfamily superfamilyb.86.1 — Hedgehog/intein (Hint) domain
Family Family familyb.86.1.2 — Intein (protein splicing domain)
Domain ID domain_idd1lwsa2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.95 — Homing endonuclease-like
Superfamily Superfamily superfamilyd.95.2 — Homing endonucleases
Family Family familyd.95.2.2 — Intein endonuclease
Domain ID domain_idd1lwsa3
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.95 — Homing endonuclease-like
Superfamily Superfamily superfamilyd.95.2 — Homing endonucleases
Family Family familyd.95.2.2 — Intein endonuclease

CATH v4.4 (3 domains)

Domain ID domain_id1lwsA01
Class class2 — Mainly Beta
Architecture architecture170 — Beta Complex
Topology topology16 — Endonuclease - Pi-scei; Chain A, domain 1
Homologous superfamily homologous superfamily10 — Hedgehog/Intein (Hint) domain
Domain ID domain_id1lwsA02
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology28 — Endonuclease I-creI
Homologous superfamily homologous superfamily10 — Homing endonucleases
Domain ID domain_id1lwsA03
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology28 — Endonuclease I-creI
Homologous superfamily homologous superfamily10 — Homing endonucleases

8. Citations (2)

9. Files and Curves (10)