MolNFT v1 · #107300 · protein
Hsmetap complex with (1-amino-2-METHYLPENTYL)PHOSPHONIC acid
4U69 · Methionine aminopeptidase 1: “Hsmetap complex with (1-amino-2-METHYLPENTYL)PHOSPHONIC acid”. X-ray diffraction, 3 ligands (Q07, CO, K), 1 pocket (best druggability 0.60). MolNFT v1 #107300 on GenesisL1: 3D structure, binding sites…
- PDB
- 4U69
- Type
- protein
- Length
- 304 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Methionine aminopeptidase 1
- EC
- 3.4.11.18
- UniProt
- P53582
- Ligands
- Q07, CO, K
- Pockets
- 1 · best druggability 0.60
Structure
x-ray diffraction · 1 distinct chain · 27% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Methionine aminopeptidase 1 (EC 3.4.11.18) | protein | 304 | 27% helix, 22% strand | P53582 |
Ligands and binding sites
- Q07 · [(1R,2S)-1-amino-2-methylpentyl]phosphonic acid · ligand · chains A
- CO · Cobalt (II) ion · metal · 2 copies · chains A
- K · Potassium ion · metal · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 302 | 0.60 | 0.78 | 37 | Q07 |
Compared structures
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P53582
- Elsewhere: RCSB PDB 4U69 · PDBe 4U69 · UniProt P53582
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