7k3d

The structure of NTMT1 in complex with compound DC1-13

Method: X-RAY DIFFRACTION Dmax: 80.0 Å Quality: GOOD

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

N-terminal Xaa-Pro-Lys N-methyltransferase 1

Homo sapiens

UniProt Q9BV86

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 B; UniProt 2–223 Not recorded SAH S-ADENOSYL-L-HOMOCYSTEINE × 1 VWP N~2~-{(2S)-1-[(naphthalen-1-yl)acetyl]-2,5-dihydro-1H-pyrrole-2-carbonyl}-L-lysyl-L-argininamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;2.5 M Ammonium sulfate; 0.1 M MES pH 6.5 Resolution 2.34 Å R-free 0.259
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 2–223 Not recorded SAH S-ADENOSYL-L-HOMOCYSTEINE × 1 VWP N~2~-{(2S)-1-[(naphthalen-1-yl)acetyl]-2,5-dihydro-1H-pyrrole-2-carbonyl}-L-lysyl-L-argininamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;2.5 M Ammonium sulfate; 0.1 M MES pH 6.5 Resolution 2.34 Å R-free 0.259

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.

17 other PDB entries and 28 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NTM1A_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 20–241; UniProt 2–223 Author chain B; PDBConstruct 20–241; UniProt 2–223

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 7k3d

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7k3d
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7k3d
Deposition date deposition_date2020-09-11
Structure title titleThe structure of NTMT1 in complex with compound DC1-13
Keywords keywordsmethyltransferase, enzyme, inhibitor complex, TRANSFERASE, transferase-transferase inhibitor complex; transferase/transferase inhibitor
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.61
Radius of gyration Rg (electron density) rg_electron23.68
Forward intensity I(0) i044943500.00
Molecular weight molecular_weight51833.0 kDa
Excluded volume excluded_volume64799 ų
Envelope volume envelope_volume75879 ų
Hydration-shell volume shell_volume27012 ų
Envelope diameter envelope_diameter79.8
Shell Rg shell_rg30.92
Envelope Rg envelope_rg23.78
Shape Rg shape_rg23.68
Total Rg total_rg24.50
Total atoms total_atoms3646
Residues n_residues442
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 dmax80.0
Rg (real space) rg_real24.61
Rg uncertainty (real space) rg_real_error0.43
I(0) (real space) i0_real4.4940e+07
I(0) uncertainty (real space) i0_real_error6.0430e+05
Rg (reciprocal space) rg_reciprocal24.61
I(0) (reciprocal space) i0_reciprocal44940000.0000
Solution quality estimate total_estimate0.8875
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary27.9
Skewness Skewness skewness0.371
Kurtosis Kurtosis kurtosis-0.394
Angular range angular_range— – 0.3250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16520000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.858; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.979; Smooth: 0.981

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)