6lpc

Crystal Structure of rat Munc18-1 with K332E/K333E mutation

Method: X-RAY DIFFRACTION Dmax: 121.0 Å Quality: GOOD

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

Syntaxin-binding protein 1

Rattus norvegicus

UniProt P61765

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–594 Chain B; UniProt 1–594 Mutation:K332E, K333E No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.6;289.15 K;4 M ammonium acetate, 0.1 M sodium acetate trihydrate Resolution 3.40 Å R-free 0.331

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.

7 other PDB entries and 9 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name STXB1_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–594; UniProt 1–594 Author chain B; PDBConstruct 1–594; UniProt 1–594

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 6lpc

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6lpc
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6lpc
Deposition date deposition_date2020-01-09
Structure title titleCrystal Structure of rat Munc18-1 with K332E/K333E mutation
Keywords keywordsSynaptic exocytosis, Membrane fusion, SNAREs-binding, EXOCYTOSIS; EXOCYTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.41
Radius of gyration Rg (electron density) rg_electron38.06
Forward intensity I(0) i0161731000.00
Molecular weight molecular_weight100920.0 kDa
Excluded volume excluded_volume125220 ų
Envelope volume envelope_volume182540 ų
Hydration-shell volume shell_volume41074 ų
Envelope diameter envelope_diameter121.0
Shell Rg shell_rg42.84
Envelope Rg envelope_rg37.26
Shape Rg shape_rg38.10
Total Rg total_rg38.27
Total atoms total_atoms7114
Residues n_residues1000
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 dmax121.0
Rg (real space) rg_real38.53
Rg uncertainty (real space) rg_real_error1.20
I(0) (real space) i0_real1.6170e+08
I(0) uncertainty (real space) i0_real_error3.0100e+06
Rg (reciprocal space) rg_reciprocal38.46
I(0) (reciprocal space) i0_reciprocal161700000.0000
Solution quality estimate total_estimate0.8770
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary35.4
Skewness Skewness skewness0.273
Kurtosis Kurtosis kurtosis-0.819
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha23670000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.911; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.922; Smooth: 0.741

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id6lpcA01
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_id6lpcA02
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_id6lpcB01
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_id6lpcB02
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

8. Citations (1)

9. Files and Curves (10)