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MolNFT v1 · #165893 · protein

MLL1 set N3861I/Q3867L bound to inhibitor 16 (tc-5109)

6U9M · Histone-lysine N-methyltransferase: “MLL1 set N3861I/Q3867L bound to inhibitor 16 (tc-5109)”. X-ray diffraction, 2 ligands (Q2M, ZN), 3 pockets (best druggability 0.69). MolNFT v1 #165893 on GenesisL1: 3D structure, binding sites…

PDB
6U9M
Type
protein
Length
297 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone-lysine N-methyltransferase
EC
2.1.1.43
UniProt
B4DIJ7
Ligands
Q2M, ZN
Pockets
3 · best druggability 0.69

Structure

x-ray diffraction · 2 distinct chains · 19% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone-lysine N-methyltransferase (EC 2.1.1.43)protein14820% helix, 34% strandB4DIJ7
BHistone-lysine N-methyltransferase (EC 2.1.1.43)protein14917% helix, 35% strandB4DIJ7

Ligands and binding sites

  • Q2M · 5'-{[(3S)-3-amino-3-carboxypropyl]({1-[(thiophen-2-yl) methyl]azetidin-3-yl}methyl)amino}-5'-deoxyadenosine · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12510.690.8537GOL
23270.580.7737Q2M
32210.480.7429Q2M

Interfaces

1 interface between chains.

  • A–B · 547 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 6U9M · MLL1 SET N3861I/Q3867L bound to inhibitor 16 (TC-5109) · the same entry in another collection · chain A against A, TM-score 1.00

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