Research workbench
Sirohydrochlorin nickelochelatase cfba in complex with cobalt- sirohydrochlorin
Analyse Sirohydrochlorin nickelochelatase cfba in complex with cobalt- sirohydrochlorin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6M2G
- Type
- protein
- Length
- 237 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- Q58380
- Ligands
- F0X
Structure
x-ray diffraction · 2 distinct chains.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 118 | — | Q58380 |
| B | — | protein | 119 | — | Q58380 |
Ligands and binding sites
- F0X · cobalt-sirohydrochlorin · ligand · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 6M2G · Sirohydrochlorin nickelochelatase CfbA in complex with cobalt-sirohydrochlorin · the same entry in another collection · chain A against A, TM-score 1.00
- Q58380 · AlphaFold monomer V2.0 prediction for sirohydrochlorin cobaltochelatase (Q58380) · a predicted model of the same protein · chain A against A, TM-score 0.99
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 Q58380
- Elsewhere: RCSB PDB 6M2G · PDBe 6M2G · UniProt Q58380
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