1skj

COCRYSTAL STRUCTURE OF UREA-SUBSTITUTED PHOSPHOPEPTIDE COMPLEX

Method: X-RAY DIFFRACTION Dmax: 49.9 Å Quality: GOOD

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

PP60 V-SRC TYROSINE KINASE TRANSFORMING PROTEIN

Rous sarcoma virus

UniProt P00524

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 142–252 Fragment:SH2 DOMAIN Mutation:N-TERMINAL INS(GS) AND C-TERMINAL INS(EFIVTD) UR2 4-[3-CARBOXYMETHYL-3-(4-PHOSPHONOOXY-BENZYL)-UREIDO]-4-[(3-CYCLOHEXYL-PROPYL)-METHYL-CARBAMOYL]BUTYRIC ACID × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;20% PEG 6K, 0.1M ODIUM CACODYLATE PH 6, HANGING DROP EXPERIMENT, PROTEIN 29 MG/ ML, INHIBITOR 4 MG/ML, 4:4:2 RATIO (WELL:PROT:INHIB), pH 6.0, vapor diffusion - hanging drop Resolution 2.00 Å R-free 0.275

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.

10 other PDB entries and 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SRC_RSVSA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–112; UniProt 142–252

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 1skj

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1skj
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1skj
Deposition date deposition_date1997-09-18
Structure title titleCOCRYSTAL STRUCTURE OF UREA-SUBSTITUTED PHOSPHOPEPTIDE COMPLEX
Keywords keywordsTYROSINE-PROTEIN KINASE, V-SRC SH2 DOMAIN, PHOSPHOTYROSINE RECOGNITION DOMAIN, PP60 SRC SH2 DOMAIN, PEPTIDOMIMETIC, UREIDO; TYROSINE-PROTEIN KINASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier14.55
Radius of gyration Rg (electron density) rg_electron13.17
Forward intensity I(0) i03095530.00
Molecular weight molecular_weight12182.0 kDa
Excluded volume excluded_volume15190 ų
Envelope volume envelope_volume16748 ų
Hydration-shell volume shell_volume10979 ų
Envelope diameter envelope_diameter50.1
Shell Rg shell_rg18.84
Envelope Rg envelope_rg13.55
Shape Rg shape_rg13.16
Total Rg total_rg14.43
Total atoms total_atoms1095
Residues n_residues102
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 dmax49.9
Rg (real space) rg_real14.48
Rg uncertainty (real space) rg_real_error0.30
I(0) (real space) i0_real3.0960e+06
I(0) uncertainty (real space) i0_real_error3.5010e+04
Rg (reciprocal space) rg_reciprocal14.49
I(0) (reciprocal space) i0_reciprocal3096000.0000
Solution quality estimate total_estimate0.8608
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.9
Skewness Skewness skewness0.226
Kurtosis Kurtosis kurtosis-0.172
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha498100.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.735; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.987

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1skja_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.93 — SH2-like
Superfamily Superfamily superfamilyd.93.1 — SH2 domain
Family Family familyd.93.1.1 — SH2 domain

CATH v4.4 (1 domains)

Domain ID domain_id1skjA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology505 — SHC Adaptor Protein
Homologous superfamily homologous superfamily10 — SH2 domain

8. Citations (2)

9. Files and Curves (10)