MolNFT v1 · #135389 · protein + DNA
Structure of Q151M complex (A62V, V75I, F77L, F116Y, Q151M) mutant HIV-1 reverse transcriptase (rt) ternary complex with a double stranded DNA and an incoming ddatp
5TXP · HIV-1 reverse transcriptase P51 subunit: “Structure of Q151M complex (A62V, V75I, F77L, F116Y, Q151M) mutant HIV-1 reverse transcriptase (rt) ternary…”. X-ray diffraction, 5 ligands (DDS, GLC, FRU), 20 pockets (best druggability…
- PDB
- 5TXP
- Type
- protein + DNA
- Length
- 2,024 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HIV-1 reverse transcriptase P51 subunit; HIV-1 reverse transcriptase P61 subunit; DNA…
- EC
- 2.7.7.49, 2.7.7.7
- UniProt
- P03366
- Ligands
- DDS, GLC, FRU, MG, SO4
- Pockets
- 20 · best druggability 0.85
Structure
x-ray diffraction · 4 distinct chains · 34% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | HIV-1 reverse transcriptase P51 subunit (EC 2.7.7.49, 2.7.7.7) | protein | 556 | 32% helix, 23% strand | P03366 |
| B, D | HIV-1 reverse transcriptase P61 subunit (EC 2.7.7.7) | protein | 412 | 35% helix, 21% strand | P03366 |
| T, E | DNA (5'- D(*TP*GP*GP*TP*CP*GP*GP*CP*GP*CP*CP*CP*GP*AP*AP*CP*AP*GP*GP*GP*AP*CP* TP*G)-3') | dna | 24 | — | — |
| P, F | DNA (5'-D(*CP*AP*GP*TP*CP*CP*CP*TP*GP*TP*TP*CP*GP*GP*(MRG) P*CP*GP*CP*CP*G)-3') | dna | 20 | — | — |
Ligands and binding sites
- DDS · 2',3'-dideoxyadenosine triphosphate · ligand · 2 copies · chains A, T, P, C, E, F
- GLC · alpha-D-glucopyranose · sugar · 2 copies · chains B, D
- FRU · beta-D-fructofuranose · sugar · 2 copies · chains B, D, F
- MG · Magnesium ion · metal · 4 copies · chains A, T, C
- SO4 · Sulfate ion · ion · chains A, B
- EDO · 1,2-ethanediol · additive · 4 copies · chains B, C, T, P, 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, 19 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1154 | 0.85 | 0.86 | 89 | EDO |
| 2 | 1025 | 0.83 | 0.84 | 84 | EDO |
| 3 | 618 | 0.82 | 0.88 | 62 | empty |
| 4 | 654 | 0.82 | 0.86 | 66 | empty |
| 5 | 369 | 0.82 | 0.91 | 39 | empty |
Interfaces
13 interfaces between chains.
- A–B · 3004 Ų buried · 38 hydrogen bonds · protein-protein
- C–D · 2970 Ų buried · 33 hydrogen bonds · protein-protein
- A–T · 1419 Ų buried · 14 hydrogen bonds · protein-nucleic
- C–E · 1284 Ų buried · 10 hydrogen bonds · protein-nucleic
- A–P · 1024 Ų buried · 11 hydrogen bonds · protein-nucleic
Modifications
Observed in the structure: 2 modified (nucleotide modification).
Compared structures
- 5TXP · STRUCTURE OF Q151M complex (A62V, V75I, F77L, F116Y, Q151M) mutant HIV-1 REVERSE… · 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
- Every structure of UniProt P03366
- Elsewhere: RCSB PDB 5TXP · PDBe 5TXP · UniProt P03366
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