Research workbench
NMR solution structure of peptide 12: first-in-class cyclic temporin L analogue with antibacterial and antibiofilm activities
Analyse NMR solution structure of peptide 12: first-in-class cyclic temporin L analogue… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7OSD
- Type
- protein
- Length
- 13 residues
- Chains
- 1
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Phe-val-pro-TRP-phe-lys-lys-phe-dle-glu-arg-ile-leu-NH2
- Ligands
- NH2
Structure
solution nmr · 1 distinct chain · 31% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Phe-val-pro-TRP-phe-lys-lys-phe-dle-glu-arg-ile-leu-NH2 | protein | 13 | 31% helix, 0% strand | — |
Ligands and binding sites
- NH2 · Amino group · ion · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Modifications
Observed in the structure: 1 d-amino, 1 isopeptide (D-amino acid, isopeptide).
Compared structures
- 7OSD · NMR Solution Structure of Peptide 12: First-in-class cyclic Temporin L analogue with… · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Elsewhere: RCSB PDB 7OSD · PDBe 7OSD
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