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MolNFT v1 · #10160 · protein

Crystal structure of saccharomyces cerevisiae N- myristoyltransferase with bound S-(2-OXO)PENTADECYLCOA and the octapeptide glyaskla

1IID · Peptide N-myristoyltransferase: “Crystal structure of saccharomyces cerevisiae N- myristoyltransferase with bound S-(2-OXO)PENTADECYLCOA and…”. X-ray diffraction, 2 ligands (NHM, NI), 5 pockets (best druggability 0.75). MolNFT v1…

PDB
1IID
Type
protein
Length
430 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptide N-myristoyltransferase; Octapeptide glyaskla
EC
2.3.1.97
UniProt
P14743
Ligands
NHM, NI
Pockets
5 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptide N-myristoyltransferase (EC 2.3.1.97)protein42227% helix, 26% strandP14743
OOctapeptide glyasklaprotein80% helix, 0% strand—

Ligands and binding sites

  • NHM · S-(2-oxo)pentadecylcoa · ligand · chains A, O
  • NI · Nickel (II) ion · metal · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16680.750.8157NHM
21270.470.7824empty
31110.440.7829empty
41150.430.7822empty
5930.390.7620empty

Interfaces

1 interface between chains.

  • A–O · 627 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 1IID · Crystal Structure of Saccharomyces cerevisiae N-myristoyltransferase with Bound… · the same entry in another collection · chain A against A, TM-score 1.00
  • P14743 · AlphaFold monomer V2.0 prediction for glycylpeptide N-tetradecanoyltransferase (P14743) · a predicted model of the same protein · chain A against A, TM-score 0.99

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