7c41

KRAS G12V and H-REV107 peptide complex

Method: X-RAY DIFFRACTION Dmax: 113.1 Å Quality: GOOD

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

GTPase KRas

Homo sapiens

UniProt P01116

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–168 Mutation:G12V HRAS-like suppressor 3 × 1 (P53816) GDP GUANOSINE-5'-DIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;polyethylene glycol 3350, 0.2 M potassium nitrate at pH 6.8 Resolution 2.28 Å R-free 0.283
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain J; UniProt 1–168 Mutation:G12V GDP GUANOSINE-5'-DIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;polyethylene glycol 3350, 0.2 M potassium nitrate at pH 6.8 Resolution 2.28 Å R-free 0.283
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain M; UniProt 1–168 Mutation:G12V GDP GUANOSINE-5'-DIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;polyethylene glycol 3350, 0.2 M potassium nitrate at pH 6.8 Resolution 2.28 Å R-free 0.283
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain G; UniProt 1–168 Mutation:G12V GDP GUANOSINE-5'-DIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;polyethylene glycol 3350, 0.2 M potassium nitrate at pH 6.8 Resolution 2.28 Å R-free 0.283

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.

445 other PDB entries and 801 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RASK_HUMAN
Isoform P01116-2
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–168; UniProt 1–168 Author chain G; PDBConstruct 1–168; UniProt 1–168 Author chain J; PDBConstruct 1–168; UniProt 1–168 Author chain M; PDBConstruct 1–168; UniProt 1–168

HRAS-like suppressor 3

OrganismNot specified

UniProt P53816

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 65–74 Not recorded GTPase KRas × 1 (P01116) GDP GUANOSINE-5'-DIPHOSPHATE × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;polyethylene glycol 3350, 0.2 M potassium nitrate at pH 6.8 Resolution 2.28 Å R-free 0.283

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.

6 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PLAT3_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain D; PDBConstruct 1–10; UniProt 65–74

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 7c41

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7c41
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7c41
Deposition date deposition_date2020-05-14
Structure title titleKRAS G12V and H-REV107 peptide complex
Keywords keywordsKRAS G12V, H-REV107, inhibitor, STRUCTURAL PROTEIN, ONCOPROTEIN-HYDROLASE complex; ONCOPROTEIN/HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier34.25
Radius of gyration Rg (electron density) rg_electron34.04
Forward intensity I(0) i0104824000.00
Molecular weight molecular_weight79112.0 kDa
Excluded volume excluded_volume97894 ų
Envelope volume envelope_volume126310 ų
Hydration-shell volume shell_volume33366 ų
Envelope diameter envelope_diameter111.9
Shell Rg shell_rg37.80
Envelope Rg envelope_rg33.99
Shape Rg shape_rg34.04
Total Rg total_rg34.30
Total atoms total_atoms5543
Residues n_residues682
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 dmax113.1
Rg (real space) rg_real34.44
Rg uncertainty (real space) rg_real_error0.96
I(0) (real space) i0_real1.0480e+08
I(0) uncertainty (real space) i0_real_error1.6020e+06
Rg (reciprocal space) rg_reciprocal34.33
I(0) (reciprocal space) i0_reciprocal104800000.0000
Solution quality estimate total_estimate0.8642
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary29.5
Skewness Skewness skewness0.407
Kurtosis Kurtosis kurtosis-0.607
Angular range angular_range— – 0.2300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha31100000.0000
Real-space data points n_real_points47
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.824; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.842; Smooth: 0.916

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id7c41A01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases
Domain ID domain_id7c41G01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases
Domain ID domain_id7c41J01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases
Domain ID domain_id7c41M01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases

8. Citations (1)

9. Files and Curves (10)