Research workbench
Crystal Structure of the 30S ribosomal subunit from a KsgA mutant of Thermus thermophilus (HB8)
Analyse Crystal Structure of the 30S ribosomal subunit from a KsgA mutant of Thermus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3OTO
- Type
- protein + RNA
- Length
- 3,900 residues
- Chains
- 21
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 3.69
- Source
- Thermus thermophilus
- Molecule
- 16S rRNA; 30S ribosomal protein S2; 30S ribosomal protein S3; 30S ribosomal protein S4…
- UniProt
- P80373, P27152, P23370, P17291, P24319, P80375, P17293, P24320, P80378, P80379, P24321, P80382, P80381, P80380, P32193
- Ligands
- MG, K, ZN
- Pockets
- 20 · best druggability 0.89
Structure
x-ray diffraction · resolution 3.69 · 21 distinct chains · 33% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 16S rRNA | rna | 1513 | — | — |
| B | 30S ribosomal protein S2 | protein | 235 | 38% helix, 13% strand | — |
| C | 30S ribosomal protein S3 | protein | 206 | 28% helix, 22% strand | — |
| D | 30S ribosomal protein S4 | protein | 208 | 40% helix, 7% strand | P80373 |
| E | 30S ribosomal protein S5 | protein | 150 | 27% helix, 37% strand | P27152 |
| F | 30S ribosomal protein S6 | protein | 101 | 32% helix, 36% strand | P23370 |
| G | 30S ribosomal protein S7 | protein | 155 | 46% helix, 5% strand | P17291 |
| H | 30S ribosomal protein S8 | protein | 138 | 29% helix, 30% strand | P24319 |
| I | 30S ribosomal protein S9 | protein | 127 | 29% helix, 21% strand | — |
| J | 30S ribosomal protein S10 | protein | 98 | 7% helix, 20% strand | P80375 |
| K | 30S ribosomal protein S11 | protein | 119 | 26% helix, 28% strand | — |
| L | 30S ribosomal protein S12 | protein | 124 | 11% helix, 19% strand | P17293 |
| M | 30S ribosomal protein S13 | protein | 115 | 50% helix, 2% strand | — |
| N | 30S ribosomal protein S14 | protein | 60 | 20% helix, 3% strand | P24320 |
| O | 30S ribosomal protein S15 | protein | 88 | 72% helix, 0% strand | P80378 |
| P | 30S ribosomal protein S16 | protein | 83 | 20% helix, 23% strand | P80379 |
| Q | 30S ribosomal protein S17 | protein | 104 | 14% helix, 37% strand | P24321 |
| R | 30S ribosomal protein S18 | protein | 73 | 34% helix, 8% strand | P80382 |
| S | 30S ribosomal protein S19 | protein | 80 | 21% helix, 15% strand | P80381 |
| T | 30S ribosomal protein S20 | protein | 99 | 73% helix, 0% strand | P80380 |
| U | 30S ribosomal protein thx | protein | 24 | 17% helix, 0% strand | P32193 |
Ligands and binding sites
- MG · Magnesium ion · metal · 94 copies · chains A, K, L, E, N, T, D, J, U, B, M
- K · Potassium ion · metal · 42 copies · chains A, I, E
- ZN · Zinc ion · metal · 2 copies · chains D, A, N
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 997 | 0.89 | 0.92 | 88 | MG, K |
| 2 | 1093 | 0.86 | 0.88 | 102 | MG |
| 3 | 1105 | 0.85 | 0.87 | 90 | MG, K |
| 4 | 836 | 0.84 | 0.87 | 83 | MG |
| 5 | 584 | 0.83 | 0.89 | 62 | MG, K |
Interfaces
42 interfaces between chains.
- A–L · 3174 Ų buried · 88 hydrogen bonds · protein-nucleic
- A–D · 3103 Ų buried · 89 hydrogen bonds · protein-nucleic
- A–I · 2963 Ų buried · 88 hydrogen bonds · protein-nucleic
- A–Q · 2864 Ų buried · 61 hydrogen bonds · protein-nucleic
- A–T · 2690 Ų buried · 63 hydrogen bonds · protein-nucleic
Modifications
Observed in the structure: 2 disulfide (disulfide).
Compared structures
- 3OTO · Crystal structure of the 30S ribosomal subunit from a ksga mutant of thermus thermophilus… · the same entry in another collection · chain K against K, 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 P80373
- Every structure of UniProt P27152
- Every structure of UniProt P23370
- Every structure of UniProt P17291
- Every structure of UniProt P24319
- Every structure of UniProt P80375
- Every structure of UniProt P17293
- Every structure of UniProt P24320
- Every structure of UniProt P80378
- Every structure of UniProt P80379
- Every structure of UniProt P24321
- Every structure of UniProt P80382
- Every structure of UniProt P80381
- Every structure of UniProt P80380
- Every structure of UniProt P32193
- Elsewhere: RCSB PDB 3OTO · PDBe 3OTO · UniProt P80373 · UniProt P27152 · UniProt P23370 · UniProt P17291 · UniProt P24319 · UniProt P80375 · UniProt P17293 · UniProt P24320 · UniProt P80378 · UniProt P80379 · UniProt P24321 · UniProt P80382 · UniProt P80381 · UniProt P80380 · UniProt P32193
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