Research workbench
Crystal structure of the regulatory subunit H of the V-type ATPase of saccharomyces cerevisiae
Analyse Crystal structure of the regulatory subunit H of the V-type ATPase of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1HO8
- Type
- protein
- Length
- 447 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Vacuolar ATP synthase subunit H
- EC
- 3.6.1.34
- UniProt
- P41807
- Ligands
- SO4
Structure
x-ray diffraction · 1 distinct chain · 74% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Vacuolar ATP synthase subunit H (EC 3.6.1.34) | protein | 447 | 74% helix, 0% strand | P41807 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 1HO8 · Crystal structure of the regulatory subunit H of the V-type ATPase of saccharomyces… · the same entry in another collection · chain A against A, TM-score 1.00
- P41807 · AlphaFold monomer V2.0 prediction for V-type proton ATPase subunit H (P41807) · a predicted model of the same protein · chain A against A, TM-score 0.78
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 P41807
- Elsewhere: RCSB PDB 1HO8 · PDBe 1HO8 · UniProt P41807
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