Research workbench
Cu-bound crystal structure of the engineered cyt CB562 variant, DICYT2, crystallized in the presence of CU(II)
Analyse Cu-bound crystal structure of the engineered cyt CB562 variant, DICYT2… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7LV1
- Type
- protein
- Length
- 212 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P0ABE7
- Ligands
- HEC, CA, CU
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| C, A | — | protein | 106 | — | P0ABE7 |
Ligands and binding sites
- HEC · Heme C · ligand · 2 copies · chains C, A
- CA · Calcium ion · metal · 4 copies · chains C, A
- CU · Copper (II) ion · metal · chains C, A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7LV1 · Cu-bound crystal structure of the engineered cyt cb562 variant, DiCyt2, crystallized in… · the same entry in another collection · chain C against C, TM-score 1.00
- P0ABE7 · AlphaFold monomer V2.0 prediction for soluble cytochrome B562 (P0ABE7) · a predicted model of the same protein · chain C 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 P0ABE7
- Elsewhere: RCSB PDB 7LV1 · PDBe 7LV1 · UniProt P0ABE7
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