2NMY
Crystal structure analysis of HIV-1 protease mutant V82A with a inhibitor saquinavir
Entity
Entity ID | Chain ID | Description | Type | Chain length | Formula weight | Number of molecules | DB Name (Accession) | Biological source | Descriptive keywords |
1 | A, B (A, B) | PROTEASE | polymer | 99 | 10712.6 | 2 | UniProt (P04587) Pfam (PF00077) UniProt (by SIFTS) (Q7SSI0) | Human immunodeficiency virus 1 | RETROPEPSIN, PR |
2 | C, G (A, B) | CHLORIDE ION | non-polymer | 35.5 | 2 | Chemie (CL) | |||
3 | D (A) | SODIUM ION | non-polymer | 23.0 | 1 | Chemie (NA) | |||
4 | E (A) | SULFATE ION | non-polymer | 96.1 | 1 | Chemie (SO4) | |||
5 | F (A) | (2S)-N-[(2S,3R)-4-[(2S,3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1 -phenyl-butan-2-yl]-2-(quinolin-2-ylcarbonylamino)butanediamide | non-polymer | 670.8 | 1 | BIRD (PRD_000454) Chemie (ROC) | |||
6 | H, I (A, B) | water | water | 18.0 | 219 | Chemie (HOH) |
Sequence modifications
A, B: 1 - 99 (UniProt: P04587)
PDB | External Database | Details |
---|---|---|
Lys 7 | Gln 506 | engineered mutation |
Ile 33 | Leu 532 | engineered mutation |
Ile 63 | Leu 562 | engineered mutation |
Ala 67 | Cys 566 | engineered mutation |
Ala 82 | Val 581 | engineered mutation |
Ala 95 | Cys 594 | engineered mutation |
Sequence viewer
Contents of the asymmetric unit
Polymers | Number of chains | 2 |
Total formula weight | 21425.2 | |
Non-Polymers* | Number of molecules | 5 |
Total formula weight | 860.8 | |
All* | Total formula weight | 22286.0 |