4wci

Crystal structure of the 1st SH3 domain from human CD2AP (CMS) in complex with a proline-rich peptide (aa 378-393) from human RIN3

Method: X-RAY DIFFRACTION Dmax: 63.4 Å Quality: GOOD

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

CD2-associated protein

Homo sapiens

UniProt Q9Y5K6

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 1–60 Fragment:UNP residues 1-60 Ras and Rab interactor 3 × 1 (Q8TB24) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 1–60 Fragment:UNP residues 1-60 Ras and Rab interactor 3 × 1 (Q8TB24) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219
3 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 1–60 Fragment:UNP residues 1-60 Ras and Rab interactor 3 × 1 (Q8TB24) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219

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.

11 other PDB entries and 34 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CD2AP_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–65; UniProt 1–60 Author chain C; PDBConstruct 6–65; UniProt 1–60 Author chain E; PDBConstruct 6–65; UniProt 1–60

Ras and Rab interactor 3

OrganismNot specified

UniProt Q8TB24

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 378–393 Not recorded CD2-associated protein × 1 (Q9Y5K6) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 378–393 Not recorded CD2-associated protein × 1 (Q9Y5K6) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219
3 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain F; UniProt 378–393 Not recorded CD2-associated protein × 1 (Q9Y5K6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Ca(ac) pH 4.2, 0.2 M Li2SO4 and 25% PEG 10 000 Resolution 1.65 Å R-free 0.219

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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RIN3_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–16; UniProt 378–393 Author chain D; PDBConstruct 1–16; UniProt 378–393 Author chain F; PDBConstruct 1–16; UniProt 378–393

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 4wci

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4wci
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id4wci
Deposition date deposition_date2014-09-04
Structure title titleCrystal structure of the 1st SH3 domain from human CD2AP (CMS) in complex with a proline-rich peptide (aa 378-393) from human RIN3
Keywords keywords;Endocytosis Adaptor protein Protein-peptide binary complex Kidney, signaling protein, Structural Genomics, Structural Genomics Consortium, SGC ;; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.69
Radius of gyration Rg (electron density) rg_electron18.77
Forward intensity I(0) i011745800.00
Molecular weight molecular_weight24820.0 kDa
Excluded volume excluded_volume30823 ų
Envelope volume envelope_volume38141 ų
Hydration-shell volume shell_volume17283 ų
Envelope diameter envelope_diameter64.8
Shell Rg shell_rg24.65
Envelope Rg envelope_rg19.26
Shape Rg shape_rg18.79
Total Rg total_rg19.62
Total atoms total_atoms1747
Residues n_residues216
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 dmax63.4
Rg (real space) rg_real19.64
Rg uncertainty (real space) rg_real_error0.44
I(0) (real space) i0_real1.1750e+07
I(0) uncertainty (real space) i0_real_error1.4410e+05
Rg (reciprocal space) rg_reciprocal19.65
I(0) (reciprocal space) i0_reciprocal11750000.0000
Solution quality estimate total_estimate0.8173
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.2
Skewness Skewness skewness0.249
Kurtosis Kurtosis kurtosis-0.431
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4674000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.878; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.988; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id4wciA00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology30 — SH3 type barrels.
Homologous superfamily homologous superfamily40 — SH3 Domains
Domain ID domain_id4wciC00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology30 — SH3 type barrels.
Homologous superfamily homologous superfamily40 — SH3 Domains
Domain ID domain_id4wciE00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology30 — SH3 type barrels.
Homologous superfamily homologous superfamily40 — SH3 Domains

8. Citations (1)

9. Files and Curves (10)