3VP2
Crystal structure of human glutaminase in complex with inhibitor 2
Summary for 3VP2
Entry DOI | 10.2210/pdb3vp2/pdb |
Related | 3VOY 3VP0 3VP1 3VP3 3VP4 3VPZ |
Descriptor | Glutaminase kidney isoform, mitochondrial, 5,5'-(sulfanediyldiethane-2,1-diyl)bis(1,3,4-thiadiazol-2-amine), SULFATE ION, ... (4 entities in total) |
Functional Keywords | hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Isoform 1: Cytoplasm, cytosol. Isoform 3: Mitochondrion: O94925 |
Total number of polymer chains | 1 |
Total formula weight | 35073.09 |
Authors | Thangavelu, K.,Sivaraman, J. (deposition date: 2012-02-23, release date: 2012-06-13, Last modification date: 2023-11-08) |
Primary citation | Thangavelu, K.,Pan, C.Q.,Karlberg, T.,Balaji, G.,Uttamchandani, M.,Suresh, V.,Schuler, H.,Low, B.C.,Sivaraman, J. Structural basis for the allosteric inhibitory mechanism of human kidney-type glutaminase (KGA) and its regulation by Raf-Mek-Erk signaling in cancer cell metabolism. Proc.Natl.Acad.Sci.USA, 109:7705-7710, 2012 Cited by PubMed: 22538822DOI: 10.1073/pnas.1116573109 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.7 Å) |
Structure validation
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