X-ray structure of macrophage inflammatory protein-1 alpha (CCL3) with heparin complex. Determined by X-ray diffraction at 3.1 Å resolution. Released 20 Apr 2016.
Explore 5D65 in 3D Show helices and sheets RCSB PDB PDBe
5D65 contains 20 α-helices and 20 β-strands across 5 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4 | 1 | 1 |
| α-helix | 8-10 | 3 | |
| α-helix | 19-21 | 3 | |
| α-helix | 22-24 | 3 | |
| β-strand | 25-30 | 6 | 2 |
| α-helix | 31-32 | 2 | |
| β-strand | 40-44 | 5 | 2 |
| β-strand | 49-52 | 4 | 2 |
| α-helix | 57-67 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-11 | 3 | 1 |
| α-helix | 19-21 | 3 | |
| α-helix | 22-24 | 3 | |
| β-strand | 25-30 | 6 | 3 |
| α-helix | 31-32 | 2 | |
| β-strand | 40-44 | 5 | 3 |
| β-strand | 49-52 | 4 | 3 |
| α-helix | 57-67 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-11 | 3 | 5 |
| α-helix | 19-20 | 2 | |
| α-helix | 22-24 | 3 | |
| β-strand | 25-30 | 6 | 6 |
| α-helix | 31-32 | 2 | |
| β-strand | 40-44 | 5 | 6 |
| β-strand | 49-52 | 4 | 6 |
| α-helix | 57-67 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-11 | 3 | 5 |
| α-helix | 19-21 | 3 | |
| α-helix | 22-24 | 3 | |
| β-strand | 25-30 | 6 | 7 |
| β-strand | 40-44 | 5 | 7 |
| β-strand | 49-52 | 4 | 7 |
| α-helix | 58-67 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| C-C motif chemokine 3 | A, B, C, D, E | protein | 70 | Homo sapiens | P10147 (AlphaFold model) |
>5D65_1 C-C motif chemokine 3 (chains A, B, C, D, E) ASLAADTPTACCFSYTSRQIPQNFIADYFETSSQCSKPGVIFLTKRSRQVCADPSEEWVQ KYVSDLELSA
Water and common crystallization additives (CL) are not listed.
Structural basis for oligomerization and glycosaminoglycan binding of CCL5 and CCL3. Liang, W.G., Triandafillou, C.G., Huang, T.Y. et al. Proc Natl Acad Sci U S A (2016) 113:5000-5005. DOI 10.1073/pnas.1523981113 · PubMed
Other PDB entries of the same protein (UniProt P10147 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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