7U1M: NTMT1

Crystal structure of NTMT1 in complex with compound YD206. Determined by X-ray diffraction at 3.17 Å resolution. Released 14 Dec 2022.

Method
X-ray diffraction
Resolution
3.17 Å
Organism
Homo sapiens
Chains
2
Atoms
3,573
Mol. weight
56.19 kDa
Ligands
SAH, KYF
Released
14 Dec 2022

Explore 7U1M in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 15 helices, 10 β-strands

ElementResiduesLengthSheet
α-helix9-2113
α-helix27-304
α-helix35-373
α-helix38-5316
α-helix59-613
β-strand64-6851
α-helix74-752
α-helix76-805
α-helix81-833
β-strand86-9161
α-helix94-10411
α-helix105-1095
β-strand111-11661
α-helix124-1252
β-strand129-13571
α-helix138-1403
α-helix143-15614
β-strand157-169131
β-strand175-17732
β-strand182-18432
β-strand18511
α-helix187-19610
β-strand201-20661
α-helix2151
β-strand216-22271
Chain B: 15 helices, 10 β-strands
ElementResiduesLengthSheet
α-helix9-2113
α-helix27-304
α-helix35-373
α-helix38-5316
α-helix59-613
β-strand64-6743
α-helix74-752
α-helix76-805
α-helix81-833
β-strand86-9163
α-helix94-10310
α-helix108-1103
β-strand111-11663
α-helix124-1252
β-strand129-13573
α-helix138-1403
α-helix143-15412
β-strand157-170143
β-strand175-17734
β-strand182-18434
β-strand185-18623
α-helix187-19610
β-strand201-20663
α-helix2151
β-strand216-22273

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
N-terminal Xaa-Pro-Lys N-methyltransferase 1A, Bprotein241Homo sapiensQ9BV86 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>7U1M_1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 (chains A, B)
MGSSHHHHHHSSGLVPRGSTSEVIEDEKQFYSKAKTYWKQIPPTVDGMLGGYGHISSIDI
NSSRKFLQRFLREGPNKTGTSCALDCGAGIGRITKRLLLPLFREVDMVDITEDFLVQAKT
YLGEEGKRVRNYFCCGLQDFTPEPDSYDVIWIQWVIGHLTDQHLAEFLRRCKGSLRPNGI
IVIKDNMAQEGVILDDVDSSVCRDLDVVRRIICSAGLSLLAEERQENLPDEIYHVYSFAL
R

Ligands and cofactors

IDNameFormulaCopies
SAHS-adenosyl-L-homocysteineC14 H20 N6 O5 S2
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 S2

Primary citation

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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