MolNFT v1 · #92485 · protein
Crystal structure of C12C TCR-HLAB2705-KK10-L6M
4G9F · HLA class I histocompatibility antigen, B-27 alpha chain: “Crystal structure of C12C TCR-HLAB2705-KK10-L6M”. X-ray diffraction, 1 ligand (SO4), 11 pockets (best druggability 0.77). MolNFT v1 #92485 on GenesisL1: 3D structure…
- PDB
- 4G9F
- Type
- protein
- Length
- 840 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, B-27 alpha chain; Beta-2-microglobulin; Gag…
- UniProt
- P03989, P61769, Q9YNZ1
- Ligands
- SO4
- Pockets
- 11 · best druggability 0.77
Structure
x-ray diffraction · 5 distinct chains · 12% helix, 44% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | HLA class I histocompatibility antigen, B-27 alpha chain | protein | 276 | 26% helix, 40% strand | P03989 |
| B | Beta-2-microglobulin | protein | 100 | 0% helix, 49% strand | P61769 |
| C | Gag protein | protein | 10 | 0% helix, 0% strand | Q9YNZ1 |
| D | Alpha chain C12C TCR | protein | 204 | 6% helix, 44% strand | — |
| E | Beta chain C12C TCR | protein | 250 | 7% helix, 49% strand | — |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 3 copies · chains A, B, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 89 | 0.77 | 0.99 | 29 | empty |
| 2 | 925 | 0.71 | 0.76 | 82 | empty |
| 3 | 650 | 0.69 | 0.77 | 51 | SO4 |
| 4 | 247 | 0.58 | 0.79 | 42 | empty |
| 5 | 269 | 0.57 | 0.78 | 42 | empty |
Interfaces
7 interfaces between chains.
- D–E · 2120 Ų buried · 29 hydrogen bonds · protein-protein
- A–B · 1335 Ų buried · 17 hydrogen bonds · protein-protein
- A–C · 994 Ų buried · 20 hydrogen bonds · protein-protein
- A–D · 411 Ų buried · 9 hydrogen bonds · protein-protein
- A–E · 308 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide (disulfide).
Compared structures
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 P03989
- Every structure of UniProt P61769
- Every structure of UniProt Q9YNZ1
- Elsewhere: RCSB PDB 4G9F · PDBe 4G9F · UniProt P03989 · UniProt P61769 · UniProt Q9YNZ1
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