2lnw

Identification and structural basis for a novel interaction between Vav2 and Arap3

Method: SOLUTION NMR Dmax: 58.7 Å Quality: GOOD

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

Guanine nucleotide exchange factor VAV2

Homo sapiens

UniProt P52735

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 659–771 Fragment:UNP RESIDUES 659-771 Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3 × 1 (Q8WWN8) SOLUTION NMR NMR measurement conditions:pH 6.2;298 K;Ionic strength (raw mmCIF value) 120;Pressure ambient NMR sample composition:1 mM [U-100% 13C; U-100% 15N] entity_1-1, 3 mM entity_2-2, 5 mM potassium phosphate-3, 20 mM sodium phosphate-4, 5 mM DTT-5, 2 mM EDTA-6, 75 mM sodium chloride-7, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:1 mM [U-100% 13C; U-100% 15N] entity_1-8, 3 mM entity_2-9, 5 mM potassium phosphate-10, 75 mM sodium chloride-11, 5 mM DTT-12, 2 mM EDTA-13, 20 mM sodium phosphate-14, 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.

6 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VAV2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 10–122; UniProt 659–771

Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3

OrganismNot specified

UniProt Q8WWN8

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 1404–1412 Fragment:UNP RESIDUES 1404-1412 Non-standard monomer:Yes (specific site not provided by mmCIF) Guanine nucleotide exchange factor VAV2 × 1 (P52735) SOLUTION NMR NMR measurement conditions:pH 6.2;298 K;Ionic strength (raw mmCIF value) 120;Pressure ambient NMR sample composition:1 mM [U-100% 13C; U-100% 15N] entity_1-1, 3 mM entity_2-2, 5 mM potassium phosphate-3, 20 mM sodium phosphate-4, 5 mM DTT-5, 2 mM EDTA-6, 75 mM sodium chloride-7, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:1 mM [U-100% 13C; U-100% 15N] entity_1-8, 3 mM entity_2-9, 5 mM potassium phosphate-10, 75 mM sodium chloride-11, 5 mM DTT-12, 2 mM EDTA-13, 20 mM sodium phosphate-14, 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.

6 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ARAP3_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–9; UniProt 1404–1412

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 2lnw

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2lnw
Deposition date deposition_date2012-01-05
Structure title titleIdentification and structural basis for a novel interaction between Vav2 and Arap3
Keywords keywordsSIGNALING PROTEIN; SIGNALING PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier15.36
Radius of gyration Rg (electron density) rg_electron14.68
Forward intensity I(0) i01192320000.00
Molecular weight molecular_weight291710.0 kDa
Excluded volume excluded_volume364020 ų
Envelope volume envelope_volume45083 ų
Hydration-shell volume shell_volume19741 ų
Envelope diameter envelope_diameter64.8
Shell Rg shell_rg26.05
Envelope Rg envelope_rg20.27
Shape Rg shape_rg14.64
Total Rg total_rg15.03
Total atoms total_atoms40540
Residues n_residues2420
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 dmax58.7
Rg (real space) rg_real15.33
Rg uncertainty (real space) rg_real_error0.43
I(0) (real space) i0_real1.1920e+09
I(0) uncertainty (real space) i0_real_error1.3330e+07
Rg (reciprocal space) rg_reciprocal15.33
I(0) (reciprocal space) i0_reciprocal1192000000.0000
Solution quality estimate total_estimate0.7843
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.1
Skewness Skewness skewness0.395
Kurtosis Kurtosis kurtosis0.326
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha666800.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.428; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.918; Smooth: 0.988

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id2lnwA01
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)