2vbl

Molecular basis of human XPC gene recognition and cleavage by engineered homing endonuclease heterodimers

Method: X-RAY DIFFRACTION Dmax: 90.5 Å Quality: REASONABLE

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

DNA ENDONUCLEASE I-CREI

CHLAMYDOMONAS REINHARDTII

UniProt P05725

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 Homooligomer Protein × 2 DNA 4 PDB declaration: hexameric(6) Consistent with all polymer counts Chain A; UniProt 1–153 Chain B; UniProt 1–153 Fragment:RESIDUES 1-153 ;5'-D(*DT*DC*DT*DG*DC*DC*DT*DT*DT*DT*DT*DT *DGP*DAP)-3' ; × 1 ;5'-D(*DT*DT*DA*DG*DG*DA*DT*DC*DC*DT*DT*DC *DAP*DAP)-3' ; × 1 5'-D(*DA*DA*DA*DA*DG*DG*DC*DA*DG*DAP)-3' × 1 5'-D(*DA*DG*DG*DA*DT*DC*DC*DT*DA*DAP)-3' × 1 MG MAGNESIUM ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;4 MG/ML PROTEIN, 35% METHANOL, 0.1M NACACODYLATE PH 6.5 Resolution 1.80 Å R-free 0.197

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.

27 other PDB entries and 30 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DNE1_CHLRE
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–153; UniProt 1–153 Author chain B; PDBConstruct 1–153; UniProt 1–153

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 2vbl

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2vbl
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id2vbl
Deposition date deposition_date2007-09-14
Structure title titleMolecular basis of human XPC gene recognition and cleavage by engineered homing endonuclease heterodimers
Keywords keywords;UV-INDUCED DNA DAMAGE, CUTTING DNA ENDONUCLEASES, PLASTID, NUCLEASE, HYDROLASE, CHLOROPLAST, ENDONUCLEASE, INTRON HOMING, AMEL3- 4_MAGNESIUM, DOUBLE STRAND BREAK (DSB), HOMING ENDONUCLEASES (HES) ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.80
Radius of gyration Rg (electron density) rg_electron24.17
Forward intensity I(0) i053828300.00
Molecular weight molecular_weight49490.0 kDa
Excluded volume excluded_volume58607 ų
Envelope volume envelope_volume70241 ų
Hydration-shell volume shell_volume25180 ų
Envelope diameter envelope_diameter88.1
Shell Rg shell_rg30.80
Envelope Rg envelope_rg24.65
Shape Rg shape_rg24.13
Total Rg total_rg24.92
Total atoms total_atoms3431
Residues n_residues352
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 dmax90.5
Rg (real space) rg_real25.00
Rg uncertainty (real space) rg_real_error0.78
I(0) (real space) i0_real5.3830e+07
I(0) uncertainty (real space) i0_real_error8.3590e+05
Rg (reciprocal space) rg_reciprocal24.96
I(0) (reciprocal space) i0_reciprocal53830000.0000
Solution quality estimate total_estimate0.6528
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.9
Skewness Skewness skewness0.561
Kurtosis Kurtosis kurtosis-0.161
Angular range angular_range— – 0.3200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6541000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.596; Stabil: 1.000; Sysdev: 0.338; Positv: 1.000; Valcen: 0.682; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd2vbla_
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.95.2.1 — Group I mobile intron endonuclease
Domain ID domain_idd2vblb_
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.95.2.1 — Group I mobile intron endonuclease

CATH v4.4 (2 domains)

Domain ID domain_id2vblA00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology28 — Endonuclease I-creI
Homologous superfamily homologous superfamily10 — Homing endonucleases
Domain ID domain_id2vblB00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology28 — Endonuclease I-creI
Homologous superfamily homologous superfamily10 — Homing endonucleases

8. Citations (1)

9. Files and Curves (10)