5IVR
Crystal Structure of HIV Protease complexed with methyl N-[(1S)-1-[[2-[(3S)-3-[(4-aminophenyl)methylamino]-4-hydroxy-butyl]phenyl]carbamoyl]-2,2-diphenyl-ethyl]carbamate
Summary for 5IVR
Entry DOI | 10.2210/pdb5ivr/pdb |
Related | 5IVQ 5IVS 5IVT |
Descriptor | Protease, CHLORIDE ION, N-{2-[(3S)-3-{[(4-aminophenyl)methyl]amino}-4-hydroxybutyl]phenyl}-Nalpha-(methoxycarbonyl)-beta-phenyl-L-phenylalaninamide, ... (4 entities in total) |
Functional Keywords | hiv, protease, hydrolase-inhibitor complex, hydrolase/inhibitor |
Biological source | Human immunodeficiency virus 1 |
Total number of polymer chains | 2 |
Total formula weight | 22370.06 |
Authors | Su, H.P. (deposition date: 2016-03-21, release date: 2016-05-18, Last modification date: 2024-03-06) |
Primary citation | Bungard, C.J.,Williams, P.D.,Ballard, J.E.,Bennett, D.J.,Beaulieu, C.,Bahnck-Teets, C.,Carroll, S.S.,Chang, R.K.,Dubost, D.C.,Fay, J.F.,Diamond, T.L.,Greshock, T.J.,Hao, L.,Holloway, M.K.,Felock, P.J.,Gesell, J.J.,Su, H.P.,Manikowski, J.J.,McKay, D.J.,Miller, M.,Min, X.,Molinaro, C.,Moradei, O.M.,Nantermet, P.G.,Nadeau, C.,Sanchez, R.I.,Satyanarayana, T.,Shipe, W.D.,Singh, S.K.,Truong, V.L.,Vijayasaradhi, S.,Wiscount, C.M.,Vacca, J.P.,Crane, S.N.,McCauley, J.A. Discovery of MK-8718, an HIV Protease Inhibitor Containing a Novel Morpholine Aspartate Binding Group. Acs Med.Chem.Lett., 7:702-707, 2016 Cited by PubMed: 27437081DOI: 10.1021/acsmedchemlett.6b00135 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.5 Å) |
Structure validation
Download full validation report