4x1v

Crystal structure of the 2nd SH3 domain from human CD2AP (CMS) in complex with a proline-rich peptide (aa 76-91) from human ARAP1

Method: X-RAY DIFFRACTION Dmax: 41.2 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 109–168 Fragment:UNP residues 109-168 Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1 × 1 (Q96P48) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;0.1 M HEPES pH 7.5, 1.4 M tri-sodium citrate dehydrate Resolution 1.58 Å R-free 0.200

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 36 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 109–168

Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1

OrganismNot specified

UniProt Q96P48

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 76–91 Fragment:UNP residues 76-91 CD2-associated protein × 1 (Q9Y5K6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;0.1 M HEPES pH 7.5, 1.4 M tri-sodium citrate dehydrate Resolution 1.58 Å R-free 0.200

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name ARAP1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–16; UniProt 76–91

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 4x1v

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4x1v
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4x1v
Deposition date deposition_date2014-11-25
Structure title titleCrystal structure of the 2nd SH3 domain from human CD2AP (CMS) in complex with a proline-rich peptide (aa 76-91) from human ARAP1
Keywords keywordsEndocytosis adaptor protein, Protein-peptide binary complex, kidney, signaling protein, 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_guinier12.85
Radius of gyration Rg (electron density) rg_electron11.32
Forward intensity I(0) i01483940.00
Molecular weight molecular_weight8249.0 kDa
Excluded volume excluded_volume10373 ų
Envelope volume envelope_volume11573 ų
Hydration-shell volume shell_volume8823 ų
Envelope diameter envelope_diameter40.0
Shell Rg shell_rg16.88
Envelope Rg envelope_rg11.79
Shape Rg shape_rg11.25
Total Rg total_rg12.99
Total atoms total_atoms577
Residues n_residues73
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 dmax41.2
Rg (real space) rg_real12.77
Rg uncertainty (real space) rg_real_error0.23
I(0) (real space) i0_real1.4840e+06
I(0) uncertainty (real space) i0_real_error1.7640e+04
Rg (reciprocal space) rg_reciprocal12.78
I(0) (reciprocal space) i0_reciprocal1484000.0000
Solution quality estimate total_estimate0.8822
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary16.1
Skewness Skewness skewness0.170
Kurtosis Kurtosis kurtosis-0.257
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha530400.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.833; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.994; Smooth: 0.973

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id4x1vA00
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)