8ygj

SpCas9-MMLV RT-pegRNA-target DNA complex (elongation 28-nt)

Method: ELECTRON MICROSCOPY Dmax: 161.4 Å Quality: GOOD

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

Gag-Pol polyprotein

Moloney murine leukemia virus

UniProt Q8UN00

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 2 DNA 3 RNA 1 PDB declaration: hexameric(6) Consistent with all polymer counts Chain E; UniProt 660–1155 Mutation:D200N, D209N, T306K, W313F, T330P, D335N RNA (137-MER) × 1 DNA (51-MER) × 1 ;DNA (5'-D(P*TP*GP*AP*TP*GP*GP*CP*AP*GP*AP*GP*TP*AP*CP*TP*AP*G)-3') ; × 1 DNA (62-MER) × 1 CRISPR-associated endonuclease Cas9/Csn1 × 1 (Q99ZW2) ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.20 Å

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.

12 other PDB entries and 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q8UN00_MLVMO
Isoform
PDB entities 4
Chains and sequence ranges Author chain E; PDBConstruct 1–496; UniProt 660–1155

CRISPR-associated endonuclease Cas9/Csn1

Streptococcus pyogenes serotype M1

UniProt Q99ZW2

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 2 DNA 3 RNA 1 PDB declaration: hexameric(6) Consistent with all polymer counts Chain A; UniProt 2–1368 Mutation:H10A, H840A RNA (137-MER) × 1 DNA (51-MER) × 1 ;DNA (5'-D(P*TP*GP*AP*TP*GP*GP*CP*AP*GP*AP*GP*TP*AP*CP*TP*AP*G)-3') ; × 1 Gag-Pol polyprotein × 1 (Q8UN00) DNA (62-MER) × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.20 Å

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.

134 other PDB entries and 146 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CAS9_STRP1
Isoform
PDB entities 6
Chains and sequence ranges Author chain A; PDBConstruct 1–1367; UniProt 2–1368

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 8ygj

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8ygj
Deposition date deposition_date2024-02-26
Structure title titleSpCas9-MMLV RT-pegRNA-target DNA complex (elongation 28-nt)
Keywords keywordsCRISPR-Cas, RNA BINDING PROTEIN-DNA-RNA COMPLEX; RNA BINDING PROTEIN/DNA/RNA
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier49.79
Radius of gyration Rg (electron density) rg_electron50.23
Forward intensity I(0) i01578570000.00
Molecular weight molecular_weight280720.0 kDa
Excluded volume excluded_volume330810 ų
Envelope volume envelope_volume519020 ų
Hydration-shell volume shell_volume88138 ų
Envelope diameter envelope_diameter169.4
Shell Rg shell_rg52.39
Envelope Rg envelope_rg48.92
Shape Rg shape_rg50.25
Total Rg total_rg50.25
Total atoms total_atoms19466
Residues n_residues2017
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 dmax161.4
Rg (real space) rg_real49.85
Rg uncertainty (real space) rg_real_error1.13
I(0) (real space) i0_real1.5790e+09
I(0) uncertainty (real space) i0_real_error2.9270e+07
Rg (reciprocal space) rg_reciprocal49.79
I(0) (reciprocal space) i0_reciprocal1578000000.0000
Solution quality estimate total_estimate0.8555
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary55.5
Skewness Skewness skewness0.373
Kurtosis Kurtosis kurtosis-0.361
Angular range angular_range— – 0.1600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha156000000.0000
Real-space data points n_real_points33
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.909; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.392

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)