3plf

Reverse Binding Mode of MetRD peptide complexed with c-Cbl TKB domain

Method: X-RAY DIFFRACTION Dmax: 85.8 Å Quality: GOOD

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

E3 ubiquitin-protein ligase CBL

Homo sapiens

UniProt P22681

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 B; UniProt 25–351 Fragment:TKB domain MetRD peptide × 1 CA CALCIUM ION × 1 CL CHLORIDE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:hanging drop;pH 6.5;298 K;100mM Bis-tris propane, 50mM ammonium sulfate, pH 6.5, hanging drop, temperature 298K Resolution 1.92 Å R-free 0.180
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 25–351 Fragment:TKB domain MetRD peptide × 1 CA CALCIUM ION × 1 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:hanging drop;pH 6.5;298 K;100mM Bis-tris propane, 50mM ammonium sulfate, pH 6.5, hanging drop, temperature 298K Resolution 1.92 Å R-free 0.180

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.

32 other PDB entries and 59 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CBL_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–329; UniProt 25–351 Author chain D; PDBConstruct 3–329; UniProt 25–351

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 3plf

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3plf
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3plf
Deposition date deposition_date2010-11-15
Structure title titleReverse Binding Mode of MetRD peptide complexed with c-Cbl TKB domain
Keywords keywordsc-Cbl TKB domain, Met, reverse binding, PROTEIN BINDING-LIGASE complex; PROTEIN BINDING/LIGASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.46
Radius of gyration Rg (electron density) rg_electron25.17
Forward intensity I(0) i078549000.00
Molecular weight molecular_weight71441.0 kDa
Excluded volume excluded_volume90338 ų
Envelope volume envelope_volume108740 ų
Hydration-shell volume shell_volume35006 ų
Envelope diameter envelope_diameter81.0
Shell Rg shell_rg33.41
Envelope Rg envelope_rg24.98
Shape Rg shape_rg25.19
Total Rg total_rg26.01
Total atoms total_atoms5028
Residues n_residues608
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 dmax85.8
Rg (real space) rg_real26.26
Rg uncertainty (real space) rg_real_error0.49
I(0) (real space) i0_real7.8550e+07
I(0) uncertainty (real space) i0_real_error1.0850e+06
Rg (reciprocal space) rg_reciprocal26.33
I(0) (reciprocal space) i0_reciprocal78550000.0000
Solution quality estimate total_estimate0.8096
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary35.7
Skewness Skewness skewness0.071
Kurtosis Kurtosis kurtosis-0.532
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha42340000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.842; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 6 domains

CATH v4.4 (6 domains)

Domain ID domain_id3plfB01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology930 — Transcription Elongation Factor S-II; Chain A
Homologous superfamily homologous superfamily20 — Adaptor protein Cbl, N-terminal domain
Domain ID domain_id3plfB02
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand
Domain ID domain_id3plfB03
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology505 — SHC Adaptor Protein
Homologous superfamily homologous superfamily10 — SH2 domain
Domain ID domain_id3plfD01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology930 — Transcription Elongation Factor S-II; Chain A
Homologous superfamily homologous superfamily20 — Adaptor protein Cbl, N-terminal domain
Domain ID domain_id3plfD02
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand
Domain ID domain_id3plfD03
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)