7cdg

Crystal structure of LSD1-CoREST in complex with PRSFLVRRR peptide

Method: X-RAY DIFFRACTION Dmax: 142.8 Å Quality: REASONABLE

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

Lysine-specific histone demethylase 1A

Homo sapiens

UniProt O60341

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 172–833 Not recorded REST corepressor 1 × 1 (Q9UKL0) PRO-ARG-SER-PHE-LEU-VAL-ARG-ARG-ARG × 1 FAD FLAVIN-ADENINE DINUCLEOTIDE × 1 GOL GLYCEROL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M N-(carbamoylmethyl)iminodiacetic acid, 1.23 M potassium sodium tartrate tetrahydrate Resolution 2.80 Å R-free 0.242

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.

126 other PDB entries and 131 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KDM1A_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 8–669; UniProt 172–833

REST corepressor 1

Homo sapiens

UniProt Q9UKL0

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 311–443 Not recorded Lysine-specific histone demethylase 1A × 1 (O60341) PRO-ARG-SER-PHE-LEU-VAL-ARG-ARG-ARG × 1 FAD FLAVIN-ADENINE DINUCLEOTIDE × 1 GOL GLYCEROL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M N-(carbamoylmethyl)iminodiacetic acid, 1.23 M potassium sodium tartrate tetrahydrate Resolution 2.80 Å R-free 0.242

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.

100 other PDB entries and 101 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RCOR1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 8–140; UniProt 311–443

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 7cdg

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7cdg
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7cdg
Deposition date deposition_date2020-06-19
Structure title titleCrystal structure of LSD1-CoREST in complex with PRSFLVRRR peptide
Keywords keywords;DEMETHYLASE, AMINE OXIDASE, CHROMATIN, HISTONE, FAD, COREPRESSOR, OXIDOREDUCTASE-TRANSCRIPTION-INHIBITOR complex, OXIDOREDUCTASE, OXIDOREDUCTASE-TRANSCRIPTION complex ;; OXIDOREDUCTASE/TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier42.93
Radius of gyration Rg (electron density) rg_electron44.21
Forward intensity I(0) i0124378000.00
Molecular weight molecular_weight90269.0 kDa
Excluded volume excluded_volume113190 ų
Envelope volume envelope_volume164080 ų
Hydration-shell volume shell_volume35799 ų
Envelope diameter envelope_diameter154.5
Shell Rg shell_rg40.82
Envelope Rg envelope_rg46.10
Shape Rg shape_rg44.22
Total Rg total_rg43.94
Total atoms total_atoms6359
Residues n_residues801
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 dmax142.8
Rg (real space) rg_real43.98
Rg uncertainty (real space) rg_real_error1.70
I(0) (real space) i0_real1.2440e+08
I(0) uncertainty (real space) i0_real_error2.3840e+06
Rg (reciprocal space) rg_reciprocal42.94
I(0) (reciprocal space) i0_reciprocal124200000.0000
Solution quality estimate total_estimate0.6256
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary30.9
Skewness Skewness skewness0.747
Kurtosis Kurtosis kurtosis-0.454
Angular range angular_range— – 0.1850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10160000.0000
Real-space data points n_real_points38
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.294; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.242; Smooth: 0.005

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)