GL1X · GenesisL1 explorer

Research workbench

Crystal structure of trmd, a tRNA-(N1G37) methyltransferase, from mycobacterium abscessus in complex with inhibitor

Analyse Crystal structure of trmd, a tRNA-(N1G37) methyltransferase, from mycobacterium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6QRD
Type
protein
Length
414 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TRNA (guanine-N(1)-)-methyltransferase
EC
2.1.1.228
UniProt
B1MDI3
Ligands
JEH, SO4
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATRNA (guanine-N(1)-)-methyltransferase (EC 2.1.1.228)protein21239% helix, 21% strandB1MDI3
BTRNA (guanine-N(1)-)-methyltransferase (EC 2.1.1.228)protein20236% helix, 22% strandB1MDI3

Ligands and binding sites

  • JEH · 5-azanyl-3-[1-[[4-[(4-propan-2-ylpiperazin-1-yl) methyl]phenyl]methyl]indol-6-yl]-1~{H}-pyrazole-4-carbonitrile · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13700.720.8357JEH
23410.710.8455JEH
31630.520.7927empty
4810.350.7513empty

Interfaces

1 interface between chains.

  • A–B · 3498 Ų buried · 77 hydrogen bonds · protein-protein

Compared structures

  • 6QRD · Crystal structure of TrmD, a tRNA-(N1G37) methyltransferase, from Mycobacterium abscessus… · the same entry in another collection · chain B against B, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.