MolNFT v1 · #33187 · protein
Structure of the calcium channel blocker omega conotoxin gvia, NMR, 20 structures
2CCO · Omega-conotoxin gvia: “Structure of the calcium channel blocker omega conotoxin gvia, NMR, 20 structures”. Solution nmr, 1 ligand (NH2). MolNFT v1 #33187 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 2CCO
- Type
- protein
- Length
- 27 residues
- Chains
- 1
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Omega-conotoxin gvia
- UniProt
- P01522
- Ligands
- NH2
Structure
solution nmr · 1 distinct chain · 0% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Omega-conotoxin gvia | protein | 27 | 0% helix, 30% strand | P01522 |
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: 3 disulfide, 3 modified (disulfide, hydroxylation).
Compared structures
- 2CCO · Structure of the calcium channel blocker omega conotoxin gvia, NMR, 20 structures · the same entry in another collection · chain A against A, TM-score 1.00
- P01522 · AlphaFold monomer V2.0 prediction for omega-conotoxin gvia (P01522) · a predicted model of the same protein · chain A against A, TM-score 0.63
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 P01522
- Elsewhere: RCSB PDB 2CCO · PDBe 2CCO · UniProt P01522
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