6php

Crystal structure of glucagon analog with 4-bromo-phenylalanine substitutions at position 6 and 22 in space group I41 at 1.65 A resolution

Method: X-RAY DIFFRACTION Dmax: 42.9 Å Quality: REASONABLE

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

Glucagon

OrganismNot specified

UniProt P01275

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 53–81 Fragment:UNP residues 53-81 Mutation:F6BrF, F22BrF Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;Tacsimate, pH 4, 16% PEG3350, 0.1 M sodium acetate, pH 4.6 Resolution 1.65 Å R-free 0.246

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.

33 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GLUC_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–29; UniProt 53–81

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 6php

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id6php
Deposition date deposition_date2019-06-25
Structure title titleCrystal structure of glucagon analog with 4-bromo-phenylalanine substitutions at position 6 and 22 in space group I41 at 1.65 A resolution
Keywords keywordsglucagon, GPCR ligand, peptide hormone, HORMONE; HORMONE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier11.75
Radius of gyration Rg (electron density) rg_electron11.17
Forward intensity I(0) i0317086.00
Molecular weight molecular_weight3115.0 kDa
Excluded volume excluded_volume3714 ų
Envelope volume envelope_volume4470 ų
Hydration-shell volume shell_volume4303 ų
Envelope diameter envelope_diameter39.6
Shell Rg shell_rg14.18
Envelope Rg envelope_rg11.41
Shape Rg shape_rg11.01
Total Rg total_rg12.43
Total atoms total_atoms402
Residues n_residues22
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 dmax42.9
Rg (real space) rg_real11.94
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real3.1710e+05
I(0) uncertainty (real space) i0_real_error3.1410e+03
Rg (reciprocal space) rg_reciprocal11.93
I(0) (reciprocal space) i0_reciprocal317100.0000
Solution quality estimate total_estimate0.7105
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary10.9
Skewness Skewness skewness0.556
Kurtosis Kurtosis kurtosis-0.290
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha24450.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.630; Stabil: 0.997; Sysdev: 1.000; Positv: 1.000; Valcen: 0.351; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (2)

9. Files and Curves (10)