Research workbench
Clm-1 mouse myeloid receptor extracellular domain
Analyse Clm-1 mouse myeloid receptor extracellular domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1ZOX
- Type
- protein
- Length
- 110 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Clm-1
- UniProt
- Q6PEU7
Structure
x-ray diffraction · 1 distinct chain · 8% helix, 50% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Clm-1 | protein | 110 | 8% helix, 50% strand | Q6PEU7 |
Modifications
Observed in the structure: 2 disulfide (disulfide).
Compared structures
- 1ZOX · CLM-1 Mouse Myeloid Receptor Extracellular Domain · the same entry in another collection · chain A against A, TM-score 1.00
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 Q6PEU7
- Elsewhere: RCSB PDB 1ZOX · PDBe 1ZOX · UniProt Q6PEU7
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