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Crystal structure of human type-I N-myristoyltransferase with bound myristoyl-CoA and inhibitor DDD90055

Analyse Crystal structure of human type-I N-myristoyltransferase with bound… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3JTK
Type
protein
Length
760 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycylpeptide N-tetradecanoyltransferase 1
EC
2.3.1.97
UniProt
P30419
Ligands
MYA, X55
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlycylpeptide N-tetradecanoyltransferase 1 (EC 2.3.1.97)protein38227% helix, 29% strandP30419
BGlycylpeptide N-tetradecanoyltransferase 1 (EC 2.3.1.97)protein37827% helix, 28% strandP30419

Ligands and binding sites

  • MYA · Tetradecanoyl-coa · ligand · 2 copies · chains A, B
  • X55 · (2R)-3-benzyl-2-(2-bromo-4-hydroxy-5-methoxyphenyl)-1,3-thiazolidin-4-one · ligand · chains A

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
110250.800.8188MYA, X55
29810.780.8089MYA
38490.770.8081empty
4620.320.7615empty

Interfaces

1 interface between chains.

  • A–B · 878 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 3JTK · Crystal Structure of human type-I N-myristoyltransferase with bound myristoyl-CoA and… · the same entry in another collection · chain A against A, TM-score 1.00
  • P30419 · AlphaFold monomer V2.0 prediction for glycylpeptide N-tetradecanoyltransferase 1 (P30419) · a predicted model of the same protein · chain A against A, TM-score 1.00

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