2fei

Solution structure of the second SH3 domain of Human CMS protein

Method: SOLUTION NMR Dmax: 48.0 Å Quality: REASONABLE

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 111–166 Fragment:The second SH3 domain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.85;295 K;Pressure 1 NMR sample composition:1.0-2.0mM 15N, 13C-labeled CMS SH3 domain, 20mM phosphate buffer (pH 6.85), 50mM sodium chloride, 90% H2O, 10% D2O | 90% H2O/10% D2O NMR sample composition:1.0-2.0mM 15N, 13C-labeled CMS SH3 domain, 20mM phosphate buffer (pH 6.85), 50mM sodium chloride, 100% D2O | 100% D2O Resolution not provided

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 2–57; UniProt 111–166

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 2fei

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2fei
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2fei
Deposition date deposition_date2005-12-15
Structure title titleSolution structure of the second SH3 domain of Human CMS protein
Keywords keywordsCMS SH3 domain, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier12.03
Radius of gyration Rg (electron density) rg_electron11.72
Forward intensity I(0) i0270136000.00
Molecular weight molecular_weight141080.0 kDa
Excluded volume excluded_volume177020 ų
Envelope volume envelope_volume19673 ų
Hydration-shell volume shell_volume11885 ų
Envelope diameter envelope_diameter50.0
Shell Rg shell_rg19.82
Envelope Rg envelope_rg15.06
Shape Rg shape_rg11.70
Total Rg total_rg12.00
Total atoms total_atoms19560
Residues n_residues1200
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 dmax48.0
Rg (real space) rg_real12.05
Rg uncertainty (real space) rg_real_error0.67
I(0) (real space) i0_real2.7010e+08
I(0) uncertainty (real space) i0_real_error3.4490e+06
Rg (reciprocal space) rg_reciprocal12.05
I(0) (reciprocal space) i0_reciprocal270100000.0000
Solution quality estimate total_estimate0.7489
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary15.2
Skewness Skewness skewness0.465
Kurtosis Kurtosis kurtosis0.495
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha109100.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.306; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.850; Smooth: 0.968

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd2feia1
Class classb — All beta proteins
Fold Fold foldb.34 — SH3-like barrel
Superfamily Superfamily superfamilyb.34.2 — SH3-domain
Family Family familyb.34.2.0 — automated matches
Domain ID domain_idd2feia2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd2feia3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id2feiA00
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)