4n3z

Crystal structure of Rabex-5delta and Rabaptin-5C21 complex

Method: X-RAY DIFFRACTION Dmax: 93.4 Å Quality: GOOD

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

Rab5 GDP/GTP exchange factor

Homo sapiens

UniProt Q9UJ41

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 132–455 Fragment:UNP residues, isoform 2, 132-455 Mutation:residues 387-408 deletion mutant Rab GTPase-binding effector protein 1 × 2 (Q15276) PO4 PHOSPHATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;289 K;2.0M NaH2PO4/K2HPO4, 0.05% n-octyl-beta-D-galactopyranoside, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 3.10 Å R-free 0.315

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.

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

View Construct and Data Evidence
UniProt name RABX5_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 9–310; UniProt 132–455

Rab GTPase-binding effector protein 1

Homo sapiens

UniProt Q15276

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 552–642 Chain C; UniProt 552–642 Fragment:UNP residues 552-642 Rab5 GDP/GTP exchange factor × 1 (Q9UJ41) PO4 PHOSPHATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;289 K;2.0M NaH2PO4/K2HPO4, 0.05% n-octyl-beta-D-galactopyranoside, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 3.10 Å R-free 0.315

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.

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

View Construct and Data Evidence
UniProt name RABE1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 2–92; UniProt 552–642 Author chain C; PDBConstruct 2–92; UniProt 552–642

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 4n3z

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4n3z
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4n3z
Deposition date deposition_date2013-10-08
Structure title titleCrystal structure of Rabex-5delta and Rabaptin-5C21 complex
Keywords keywordsRab5, Rabex-5, Rabaptin-5, GEF activity, endocytosis, early endosome; ENDOCYTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.87
Radius of gyration Rg (electron density) rg_electron27.34
Forward intensity I(0) i035908300.00
Molecular weight molecular_weight44000.0 kDa
Excluded volume excluded_volume54266 ų
Envelope volume envelope_volume75816 ų
Hydration-shell volume shell_volume24785 ų
Envelope diameter envelope_diameter95.1
Shell Rg shell_rg32.40
Envelope Rg envelope_rg27.60
Shape Rg shape_rg27.29
Total Rg total_rg28.04
Total atoms total_atoms3074
Residues n_residues403
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 dmax93.4
Rg (real space) rg_real27.95
Rg uncertainty (real space) rg_real_error0.91
I(0) (real space) i0_real3.5910e+07
I(0) uncertainty (real space) i0_real_error5.3410e+05
Rg (reciprocal space) rg_reciprocal27.93
I(0) (reciprocal space) i0_reciprocal35910000.0000
Solution quality estimate total_estimate0.8926
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.8
Skewness Skewness skewness0.374
Kurtosis Kurtosis kurtosis-0.339
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3358000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.898; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.940; Smooth: 0.971

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4n3zb_
Class classh — Coiled coil proteins
Fold Fold foldh.1 — Parallel coiled-coil
Superfamily Superfamily superfamilyh.1.27 — G protein-binding domain
Family Family familyh.1.27.2 — Rabaptin-5
Domain ID domain_idd4n3zc_
Class classh — Coiled coil proteins
Fold Fold foldh.1 — Parallel coiled-coil
Superfamily Superfamily superfamilyh.1.27 — G protein-binding domain
Family Family familyh.1.27.2 — Rabaptin-5

CATH v4.4 (1 domains)

Domain ID domain_id4n3zA02
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1050 — Glutathione S-transferase Yfyf (Class Pi); Chain A, domain 2
Homologous superfamily homologous superfamily80 — VPS9 domain

8. Citations (1)

9. Files and Curves (10)