Research workbench
Crystal structure of chaetomium thermophilum VPS29 complexed with rapid-derived cyclic peptide rt-D3
Analyse Crystal structure of chaetomium thermophilum VPS29 complexed with rapid-derived… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6XS8
- Type
- protein
- Length
- 196 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Vacuolar protein sorting-associated protein 29…
- UniProt
- G0RZB5
- Ligands
- 48V
Structure
x-ray diffraction · 2 distinct chains · 13% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Vacuolar protein sorting-associated protein 29 | protein | 184 | 14% helix, 40% strand | G0RZB5 |
| B | 48V-dty-gly-tyr-asp-pro-leu-gly-leu-lys-tyr-phe-ala | protein | 12 | 0% helix, 17% strand | — |
Ligands and binding sites
- 48V · {[(2R)-2,3-diamino-3-oxopropyl]sulfanyl}acetic acid · ligand · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
1 interface between chains.
- A–B · 420 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 covalent, 1 d-amino (covalent ligand, D-amino acid).
Compared structures
- 6XS8 · Crystal structure of Chaetomium thermophilum Vps29 complexed with RaPID-derived cyclic… · 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
- Every structure of UniProt G0RZB5
- Elsewhere: RCSB PDB 6XS8 · PDBe 6XS8 · UniProt G0RZB5
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