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T. thermophilus transcription initiation complex having a rrr discriminator sequence and a nontemplate-strand length corresponding to tss selection at position 7 (rpo-ggg-7)
Analyse T. thermophilus transcription initiation complex having a rrr discriminator… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5E17
- Type
- protein + DNA + RNA
- Length
- 3,531 residues
- Chains
- 9
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA-directed RNA polymerase subunit alpha; DNA-directed RNA polymerase subunit beta…
- EC
- 2.7.7.6
- UniProt
- Q9Z9H6, Q8RQE9, Q8RQE8, Q8RQE7, Q5SKW1
- Ligands
- MG, ZN
- Pockets
- 20 · best druggability 0.86
Structure
x-ray diffraction · 9 distinct chains · 36% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA-directed RNA polymerase subunit alpha (EC 2.7.7.6) | protein | 231 | 22% helix, 43% strand | Q9Z9H6 |
| B | DNA-directed RNA polymerase subunit alpha (EC 2.7.7.6) | protein | 222 | 20% helix, 40% strand | Q9Z9H6 |
| C | DNA-directed RNA polymerase subunit beta (EC 2.7.7.6) | protein | 1112 | 30% helix, 27% strand | Q8RQE9 |
| D | DNA-directed RNA polymerase subunit beta' (EC 2.7.7.6) | protein | 1486 | 36% helix, 24% strand | Q8RQE8 |
| E | DNA-directed RNA polymerase subunit omega (EC 2.7.7.6) | protein | 94 | 48% helix, 12% strand | Q8RQE7 |
| F | RNA polymerase sigma factor siga | protein | 337 | 71% helix, 1% strand | Q5SKW1 |
| G | DNA (5'- D(*CP*CP*T*GP*CP*AP*TP*CP*CP*GP*TP*GP*AP*GP*TP*CP*GP*AP*GP*GP*G)-3') | dna | 18 | — | — |
| H | DNA (27-mer) | dna | 24 | — | — |
| I | RNA (5'-R(*CP*CP*CP*UP*CP*GP*A)-3') | rna | 7 | — | — |
Ligands and binding sites
- MG · Magnesium ion · metal · 4 copies · chains B, D, I, F
- ZN · Zinc ion · metal · 2 copies · chains D
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 | 1056 | 0.86 | 0.87 | 99 | MG |
| 2 | 772 | 0.85 | 0.89 | 82 | empty |
| 3 | 1041 | 0.85 | 0.86 | 91 | empty |
| 4 | 748 | 0.85 | 0.88 | 81 | empty |
| 5 | 442 | 0.78 | 0.86 | 55 | empty |
Interfaces
22 interfaces between chains.
- C–D · 8904 Ų buried · 130 hydrogen bonds · protein-protein
- D–F · 3933 Ų buried · 54 hydrogen bonds · protein-protein
- C–F · 2416 Ų buried · 23 hydrogen bonds · protein-protein
- D–E · 2370 Ų buried · 32 hydrogen bonds · protein-protein
- A–C · 2065 Ų buried · 42 hydrogen bonds · protein-protein
Compared structures
- 5E17 · T. thermophilus transcription initiation complex having a RRR discriminator sequence and… · the same entry in another collection · chain H against H, TM-score 1.00
- Q8RQE7 · AlphaFold monomer V2.0 prediction for DNA-directed RNA polymerase subunit omega (Q8RQE7) · a predicted model of the same protein · chain E against A, TM-score 0.98
- Q9Z9H6 · AlphaFold monomer V2.0 prediction for DNA-directed RNA polymerase subunit alpha (Q9Z9H6) · a predicted model of the same protein · chain A against A, TM-score 0.95
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 Q9Z9H6
- Every structure of UniProt Q8RQE9
- Every structure of UniProt Q8RQE8
- Every structure of UniProt Q8RQE7
- Every structure of UniProt Q5SKW1
- Elsewhere: RCSB PDB 5E17 · PDBe 5E17 · UniProt Q9Z9H6 · UniProt Q8RQE9 · UniProt Q8RQE8 · UniProt Q8RQE7 · UniProt Q5SKW1
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