Research workbench
Crystal structure of mbl collagen-like peptide
Analyse Crystal structure of mbl collagen-like peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3POD
- Type
- protein
- Length
- 72 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Mbl collagen-like peptide
- Ligands
- ACE, NH2
Structure
x-ray diffraction · 1 distinct chain · 0% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Mbl collagen-like peptide | protein | 24 | 0% helix, 0% strand | — |
Ligands and binding sites
- ACE · Acetyl group · ligand · 3 copies · chains A, B, C
- NH2 · Amino group · ion · 2 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
3 interfaces between chains.
- B–C · 752 Ų buried · 7 hydrogen bonds · protein-protein
- A–B · 747 Ų buried · 7 hydrogen bonds · protein-protein
- A–C · 705 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 21 modified, 3 covalent (hydroxylation, covalent ligand).
Compared structures
- 3POD · Crystal structure of MBL collagen-like peptide · 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
- Elsewhere: RCSB PDB 3POD · PDBe 3POD
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