1kc2

structure of the triple (Lys(beta)D3Ala, Asp(beta)C8Ala, AspCD2Ala) mutant of the Src SH2 domain bound to the PQpYEEIPI peptide

Method: X-RAY DIFFRACTION Dmax: 46.4 Å Quality: GOOD

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

Src Tyrosine kinase

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 145–247 Fragment:SH2 domain Mutation:D190A, D192A, K200A PQpYEEIPI peptide × 1 CO COBALT (II) ION × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.10 Å R-free 0.267

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 1–103; UniProt 145–247

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 1kc2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1kc2
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1kc2
Deposition date deposition_date2001-11-07
Structure title titlestructure of the triple (Lys(beta)D3Ala, Asp(beta)C8Ala, AspCD2Ala) mutant of the Src SH2 domain bound to the PQpYEEIPI peptide
Keywords keywordsSH2 domain, phosphotyrosine, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier14.23
Radius of gyration Rg (electron density) rg_electron12.72
Forward intensity I(0) i03060860.00
Molecular weight molecular_weight11886.0 kDa
Excluded volume excluded_volume14733 ų
Envelope volume envelope_volume16299 ų
Hydration-shell volume shell_volume10891 ų
Envelope diameter envelope_diameter44.2
Shell Rg shell_rg18.50
Envelope Rg envelope_rg13.08
Shape Rg shape_rg12.67
Total Rg total_rg14.12
Total atoms total_atoms834
Residues n_residues103
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 dmax46.4
Rg (real space) rg_real14.12
Rg uncertainty (real space) rg_real_error0.28
I(0) (real space) i0_real3.0610e+06
I(0) uncertainty (real space) i0_real_error3.3970e+04
Rg (reciprocal space) rg_reciprocal14.13
I(0) (reciprocal space) i0_reciprocal3061000.0000
Solution quality estimate total_estimate0.8737
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary19.4
Skewness Skewness skewness0.113
Kurtosis Kurtosis kurtosis-0.315
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha711300.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.790; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.987

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1kc2a_
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_id1kc2A00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology505 — SHC Adaptor Protein
Homologous superfamily homologous superfamily10 — SH2 domain

8. Citations (1)

9. Files and Curves (10)