7t1u

Crystal structure of a superbinder Src SH2 domain (sSrcF) in complex with a high affinity phosphopeptide

Method: X-RAY DIFFRACTION Dmax: 74.9 Å Quality: GOOD

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

Proto-oncogene tyrosine-protein kinase Src

Homo sapiens

UniProt P12931

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 147–251 Fragment:SH2 domain Mutation:Residues 180 to 188 mutated from SETTKGAYC to GQSQPDYV and K206I (numbered as residue 205 in these coordinates) Synthetic phosphopeptide × 1 ZN ZINC ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4;293 K;80 uM Zinc Acetate, 12% PEG3350, 100 mM Sodium Acetate (pH 4.0), and 2% 1,3-butanediol Resolution 2.65 Å R-free 0.270
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 147–251 Fragment:SH2 domain Mutation:Residues 180 to 188 mutated from SETTKGAYC to GQSQPDYV and K206I (numbered as residue 205 in these coordinates) Synthetic phosphopeptide × 1 ZN ZINC ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4;293 K;80 uM Zinc Acetate, 12% PEG3350, 100 mM Sodium Acetate (pH 4.0), and 2% 1,3-butanediol Resolution 2.65 Å R-free 0.270

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.

76 other PDB entries and 100 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SRC_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–109; UniProt 147–251 Author chain B; PDBConstruct 6–109; UniProt 147–251

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 7t1u

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7t1u
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7t1u
Deposition date deposition_date2021-12-02
Structure title titleCrystal structure of a superbinder Src SH2 domain (sSrcF) in complex with a high affinity phosphopeptide
Keywords keywordsSrc Homology 2 (SH2), rationally engineered, phosphotyrosine, SIGNALING PROTEIN; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.04
Radius of gyration Rg (electron density) rg_electron19.92
Forward intensity I(0) i012179800.00
Molecular weight molecular_weight25338.0 kDa
Excluded volume excluded_volume31292 ų
Envelope volume envelope_volume38174 ų
Hydration-shell volume shell_volume16817 ų
Envelope diameter envelope_diameter74.4
Shell Rg shell_rg25.15
Envelope Rg envelope_rg19.97
Shape Rg shape_rg19.82
Total Rg total_rg20.97
Total atoms total_atoms1777
Residues n_residues224
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 dmax74.9
Rg (real space) rg_real21.11
Rg uncertainty (real space) rg_real_error0.62
I(0) (real space) i0_real1.2180e+07
I(0) uncertainty (real space) i0_real_error1.5000e+05
Rg (reciprocal space) rg_reciprocal21.10
I(0) (reciprocal space) i0_reciprocal12180000.0000
Solution quality estimate total_estimate0.8321
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.7
Skewness Skewness skewness0.423
Kurtosis Kurtosis kurtosis-0.356
Angular range angular_range— – 0.3800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2904000.0000
Real-space data points n_real_points70
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.649; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.868; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)