Research workbench
Crystal structure of human N-acetylserotonin methyltransferase (asmt) in complex with SAM
Analyse Crystal structure of human N-acetylserotonin methyltransferase (asmt) in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4A6D
- Type
- protein
- Length
- 346 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P46597
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 346 | — | P46597 |
Compared structures
- 4A6D · Crystal structure of human N-acetylserotonin methyltransferase (ASMT) in complex with SAM · the same entry in another collection · chain A against A, TM-score 1.00
- P46597 · AlphaFold monomer V2.0 prediction for acetylserotonin O-methyltransferase (P46597) · a predicted model of the same protein · chain A against A, TM-score 0.97
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 P46597
- Elsewhere: RCSB PDB 4A6D · PDBe 4A6D · UniProt P46597
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