Crystal structure of NTMT1 in complex with compound YD206. Determined by X-ray diffraction at 3.17 Å resolution. Released 14 Dec 2022.
Explore 7U1M in 3D Show helices and sheets RCSB PDB PDBe
7U1M contains 30 α-helices and 20 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 9-21 | 13 | |
| α-helix | 27-30 | 4 | |
| α-helix | 35-37 | 3 | |
| α-helix | 38-53 | 16 | |
| α-helix | 59-61 | 3 | |
| β-strand | 64-68 | 5 | 1 |
| α-helix | 74-75 | 2 | |
| α-helix | 76-80 | 5 | |
| α-helix | 81-83 | 3 | |
| β-strand | 86-91 | 6 | 1 |
| α-helix | 94-104 | 11 | |
| α-helix | 105-109 | 5 | |
| β-strand | 111-116 | 6 | 1 |
| α-helix | 124-125 | 2 | |
| β-strand | 129-135 | 7 | 1 |
| α-helix | 138-140 | 3 | |
| α-helix | 143-156 | 14 | |
| β-strand | 157-169 | 13 | 1 |
| β-strand | 175-177 | 3 | 2 |
| β-strand | 182-184 | 3 | 2 |
| β-strand | 185 | 1 | 1 |
| α-helix | 187-196 | 10 | |
| β-strand | 201-206 | 6 | 1 |
| α-helix | 215 | 1 | |
| β-strand | 216-222 | 7 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 9-21 | 13 | |
| α-helix | 27-30 | 4 | |
| α-helix | 35-37 | 3 | |
| α-helix | 38-53 | 16 | |
| α-helix | 59-61 | 3 | |
| β-strand | 64-67 | 4 | 3 |
| α-helix | 74-75 | 2 | |
| α-helix | 76-80 | 5 | |
| α-helix | 81-83 | 3 | |
| β-strand | 86-91 | 6 | 3 |
| α-helix | 94-103 | 10 | |
| α-helix | 108-110 | 3 | |
| β-strand | 111-116 | 6 | 3 |
| α-helix | 124-125 | 2 | |
| β-strand | 129-135 | 7 | 3 |
| α-helix | 138-140 | 3 | |
| α-helix | 143-154 | 12 | |
| β-strand | 157-170 | 14 | 3 |
| β-strand | 175-177 | 3 | 4 |
| β-strand | 182-184 | 3 | 4 |
| β-strand | 185-186 | 2 | 3 |
| α-helix | 187-196 | 10 | |
| β-strand | 201-206 | 6 | 3 |
| α-helix | 215 | 1 | |
| β-strand | 216-222 | 7 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| N-terminal Xaa-Pro-Lys N-methyltransferase 1 | A, B | protein | 241 | Homo sapiens | Q9BV86 (AlphaFold model) |
>7U1M_1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 (chains A, B) MGSSHHHHHHSSGLVPRGSTSEVIEDEKQFYSKAKTYWKQIPPTVDGMLGGYGHISSIDI NSSRKFLQRFLREGPNKTGTSCALDCGAGIGRITKRLLLPLFREVDMVDITEDFLVQAKT YLGEEGKRVRNYFCCGLQDFTPEPDSYDVIWIQWVIGHLTDQHLAEFLRRCKGSLRPNGI IVIKDNMAQEGVILDDVDSSVCRDLDVVRRIICSAGLSLLAEERQENLPDEIYHVYSFAL R
| ID | Name | Formula | Copies |
|---|---|---|---|
| SAH | S-adenosyl-L-homocysteine | C14 H20 N6 O5 S | 2 |
| KYF | (1R,3S,4R)-1-azabicyclo[2.2.2]octan-3-yl {2-[2-(4-fluorophenyl)-1,3-thiazol-4-y… | C20 H24 F N3 O2 S | 2 |
Venglustat Inhibits Protein N-Terminal Methyltransferase 1 in a Substrate-Competitive Manner. Dong, G., Deng, Y., Yasgar, A. et al. J Med Chem (2022) 65:12334-12345. DOI 10.1021/acs.jmedchem.2c01050 · PubMed
Other PDB entries of the same protein (UniProt Q9BV86 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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