5axw

Crystal structure of Staphylococcus aureus Cas9 in complex with sgRNA and target DNA (TTGGGT PAM)

Method: X-RAY DIFFRACTION Dmax: 120.7 Å Quality: GOOD

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

CRISPR-associated endonuclease Cas9

Staphylococcus aureus subsp. aureus

UniProt J7RUA5

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 Monomer Protein × 1 DNA 2 RNA 1 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain A; UniProt 1–1053 Mutation:N580A/C946A RNA (73-MER) × 1 DNA (28-MER) × 1 ;DNA (5'-D(*TP*TP*GP*GP*GP*TP*AP*G)-3') ; × 1 NA SODIUM ION × 4 PO4 PHOSPHATE ION × 1 EDO 1,2-ETHANEDIOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;PEG4000, NaCl, Na2HPO4, NaN3 Resolution 2.70 Å R-free 0.230

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 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name J7RUA5_STAAU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–1056; UniProt 1–1053

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 5axw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5axw
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5axw
Deposition date deposition_date2015-08-01
Structure title titleCrystal structure of Staphylococcus aureus Cas9 in complex with sgRNA and target DNA (TTGGGT PAM)
Keywords keywordsCRISPR-Cas9, genome engineering, HYDROLASE-RNA-DNA complex; HYDROLASE/RNA/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier37.13
Radius of gyration Rg (electron density) rg_electron37.12
Forward intensity I(0) i0474425000.00
Molecular weight molecular_weight153870.0 kDa
Excluded volume excluded_volume182630 ų
Envelope volume envelope_volume253930 ų
Hydration-shell volume shell_volume55966 ų
Envelope diameter envelope_diameter126.8
Shell Rg shell_rg44.34
Envelope Rg envelope_rg36.29
Shape Rg shape_rg37.16
Total Rg total_rg37.43
Total atoms total_atoms10705
Residues n_residues1152
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 dmax120.7
Rg (real space) rg_real37.03
Rg uncertainty (real space) rg_real_error1.12
I(0) (real space) i0_real4.7440e+08
I(0) uncertainty (real space) i0_real_error9.0490e+06
Rg (reciprocal space) rg_reciprocal37.09
I(0) (reciprocal space) i0_reciprocal474500000.0000
Solution quality estimate total_estimate0.8969
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary44.9
Skewness Skewness skewness0.228
Kurtosis Kurtosis kurtosis-0.477
Angular range angular_range— – 0.2150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha52150000.0000
Real-space data points n_real_points44
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.916; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.910

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd5axwa1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.55 — Ribonuclease H-like motif
Superfamily Superfamily superfamilyc.55.3 — Ribonuclease H-like
Family Family familyc.55.3.16 — RuvC-like domain from CRISPR-associated protein Cas9
Domain ID domain_idd5axwa2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.4 — His-Me finger endonucleases
Superfamily Superfamily superfamilyd.4.1 — His-Me finger endonucleases
Family Family familyd.4.1.8 — HNH domain from CRISPR-associated protein Cas9
Domain ID domain_idd5axwa3
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.393 — CRISPR-associated endonuclease Cas9/Csn1, Target recognition (REC) lobe
Superfamily Superfamily superfamilyd.393.1 — CRISPR-associated endonuclease Cas9/Csn1, Target recognition (REC) lobe
Family Family familyd.393.1.1 — CRISPR-associated endonuclease Cas9/Csn1, Target recognition (REC) lobe
Domain ID domain_idd5axwa4
Class classe — Multi-domain proteins (alpha and beta)
Fold Fold folde.80 — CRISPR-associated endonuclease Cas9/Csn1, Protospace-adjacent motif (PAM)-interacting domain
Superfamily Superfamily superfamilye.80.1 — CRISPR-associated endonuclease Cas9/Csn1, PAM-interacting (PI) domain
Family Family familye.80.1.1 — CRISPR-associated endonuclease Cas9/Csn1, PAM-interacting (PI) domain

8. Citations (1)

9. Files and Curves (10)