MolNFT v1 · #8911 · protein
Structure of 3-isopropylmalate dehydrogenase in complex with NAD+: ligand-induced loop-closing and mechanism for cofactor specificity
1HEX: “Structure of 3-isopropylmalate dehydrogenase in complex with NAD+: ligand-induced loop-closing and mechanism…”. X-ray diffraction. MolNFT v1 #8911 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1HEX
- Type
- protein
- Length
- 345 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- Q5SIY4
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 345 | — | Q5SIY4 |
Compared structures
- 1HEX · Structure of 3-isopropylmalate dehydrogenase in complex with NAD+: ligand-induced… · the same entry in another collection · chain A against A, TM-score 1.00
- Q5SIY4 · AlphaFold monomer V2.0 prediction for 3-isopropylmalate dehydrogenase (Q5SIY4) · a predicted model of the same protein · chain A against A, TM-score 0.95
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 Q5SIY4
- Elsewhere: RCSB PDB 1HEX · PDBe 1HEX · UniProt Q5SIY4
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