5bv1

Crystal Structure of a Vps33-Vps16 Complex from Chaetomium thermophilum

Method: X-RAY DIFFRACTION Dmax: 137.8 Å Quality: GOOD

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

VPS33

Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719)

UniProt G0SCM5

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 139–806 Fragment:unp residues 139-806 Putative vacuolar protein sorting-associated protein × 1 (G0S6M7) MLT D-MALATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;HEPES buffer, 8-10% w/v PEG 5000 monomethyl ether Resolution 2.90 Å R-free 0.276
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 139–806 Fragment:unp residues 139-806 Putative vacuolar protein sorting-associated protein × 1 (G0S6M7) MLT D-MALATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;HEPES buffer, 8-10% w/v PEG 5000 monomethyl ether Resolution 2.90 Å R-free 0.276

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 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name G0SCM5_CHATD
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–669; UniProt 139–806 Author chain C; PDBConstruct 2–669; UniProt 139–806

Putative vacuolar protein sorting-associated protein

Chaetomium thermophilum

UniProt G0S6M7

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 505–816 Fragment:unp residues 503-816 Mutation:L672V VPS33 × 1 (G0SCM5) MLT D-MALATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;HEPES buffer, 8-10% w/v PEG 5000 monomethyl ether Resolution 2.90 Å R-free 0.276
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 505–816 Fragment:unp residues 503-816 Mutation:L672V VPS33 × 1 (G0SCM5) MLT D-MALATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;HEPES buffer, 8-10% w/v PEG 5000 monomethyl ether Resolution 2.90 Å R-free 0.276

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.

3 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name G0S6M7_CHATD
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 4–333; UniProt 505–816 Author chain D; PDBConstruct 4–333; UniProt 505–816

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 5bv1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5bv1
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id5bv1
Deposition date deposition_date2015-06-04
Structure title titleCrystal Structure of a Vps33-Vps16 Complex from Chaetomium thermophilum
Keywords keywordsMembrane trafficking, SM protein, HOPS complex, thermophile, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier44.43
Radius of gyration Rg (electron density) rg_electron43.82
Forward intensity I(0) i0601297000.00
Molecular weight molecular_weight202360.0 kDa
Excluded volume excluded_volume253940 ų
Envelope volume envelope_volume369450 ų
Hydration-shell volume shell_volume69831 ų
Envelope diameter envelope_diameter140.0
Shell Rg shell_rg49.48
Envelope Rg envelope_rg42.35
Shape Rg shape_rg43.81
Total Rg total_rg44.15
Total atoms total_atoms14259
Residues n_residues1797
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 dmax137.8
Rg (real space) rg_real44.33
Rg uncertainty (real space) rg_real_error0.83
I(0) (real space) i0_real6.0130e+08
I(0) uncertainty (real space) i0_real_error1.0020e+07
Rg (reciprocal space) rg_reciprocal44.43
I(0) (reciprocal space) i0_reciprocal601400000.0000
Solution quality estimate total_estimate0.8827
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary49.8
Skewness Skewness skewness0.203
Kurtosis Kurtosis kurtosis-0.607
Angular range angular_range— – 0.1800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha50890000.0000
Real-space data points n_real_points37
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.967; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.571

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 8 domains

CATH v4.4 (8 domains)

Domain ID domain_id5bv1A01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2060 — Sec1/Munc18 (SM) protein, domain 1
Domain ID domain_id5bv1A02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1910 — Sec1/Munc18 (SM) protein, domain 2
Domain ID domain_id5bv1A03
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology830 — Syntaxin Binding Protein 1; Chain A, domain 2
Homologous superfamily homologous superfamily10 — Sec1/Munc18 (SM) protein, domain 3a
Domain ID domain_id5bv1A04
Class class1 — Mainly Alpha
Architecture architecture25 — Alpha Horseshoe
Topology topology40 — Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat
Homologous superfamily homologous superfamily850 — Sec1/Munc18 (SM) protein, domain 3b
Domain ID domain_id5bv1C01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2060 — Sec1/Munc18 (SM) protein, domain 1
Domain ID domain_id5bv1C02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1910 — Sec1/Munc18 (SM) protein, domain 2
Domain ID domain_id5bv1C03
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology830 — Syntaxin Binding Protein 1; Chain A, domain 2
Homologous superfamily homologous superfamily10 — Sec1/Munc18 (SM) protein, domain 3a
Domain ID domain_id5bv1C04
Class class1 — Mainly Alpha
Architecture architecture25 — Alpha Horseshoe
Topology topology40 — Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat
Homologous superfamily homologous superfamily850 — Sec1/Munc18 (SM) protein, domain 3b

8. Citations (2)

9. Files and Curves (10)