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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
6QRB
Type
protein
Length
425 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.66
Source
Mycobacterium abscessus
Molecule
tRNA (guanine-N(1)-)-methyltransferase
EC
2.1.1.228
UniProt
B1MDI3
Ligands
JEQ
Pockets
5 · best druggability 0.76

Structure

x-ray diffraction · resolution 1.66 · 2 distinct chains · 36% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AtRNA (guanine-N(1)-)-methyltransferase (EC 2.1.1.228)protein22037% helix, 20% strandB1MDI3
BtRNA (guanine-N(1)-)-methyltransferase (EC 2.1.1.228)protein20535% helix, 22% strandB1MDI3

Ligands and binding sites

  • JEQ · 5-azanyl-3-[1-[[(3~{R})-1-(phenylmethyl)piperidin-3-yl]methyl]indol-6-yl]-1~{H}-pyrazole-4-carbonitrile · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16690.760.8280JEQ
23290.720.8450JEQ
31880.520.7828empty
41420.510.7916empty
5550.280.7513empty

Interfaces

1 interface between chains.

  • A–B · 3603 Ų buried · 76 hydrogen bonds · protein-protein

Compared structures

  • 6QRB · Crystal structure of trmd, a tRNA-(N1G37) methyltransferase, from mycobacterium abscessus… · the same entry in another collection · chain A against A, TM-score 1.00

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