Research workbench
NMR solution structure of designed peptide NC_EHE_D1
Analyse NMR solution structure of designed peptide NC_EHE_D1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5KWO
- Type
- protein
- Length
- 26 residues
- Chains
- 1
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Designed peptide NC_EHE_D1
Structure
solution nmr · 1 distinct chain · 42% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Designed peptide NC_EHE_D1 | protein | 26 | 42% helix, 23% strand | — |
Modifications
Observed in the structure: 2 d-amino, 2 disulfide (D-amino acid, disulfide).
Compared structures
- 5KWO · NMR Solution Structure of Designed Peptide NC_EHE_D1 · 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 5KWO · PDBe 5KWO
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