8E0D
Crystal structure of human Sar1bE140D
Summary for 8E0D
| Entry DOI | 10.2210/pdb8e0d/pdb |
| Related | 8E0A |
| Descriptor | GTP-binding protein SAR1b, GUANOSINE-5',3'-TETRAPHOSPHATE (3 entities in total) |
| Functional Keywords | sar1b, ppgpp, copii, small gtpase, signaling protein |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 23025.00 |
| Authors | Huang, Q. (deposition date: 2022-08-08, release date: 2022-11-30, Last modification date: 2023-10-25) |
| Primary citation | Huang, Q.,Szebenyi, D.M.E. The alarmone ppGpp selectively inhibits the isoform A of the human small GTPase Sar1. Proteins, 91:518-531, 2023 Cited by PubMed Abstract: Transport of newly synthesized proteins from endoplasmic reticulum (ER) to Golgi is mediated by coat protein complex II (COPII). The assembly and disassembly of COPII vesicles is regulated by the molecular switch Sar1, which is a small GTPase and a component of COPII. Usually a small GTPase binds GDP (inactive form) or GTP (active form). Mammals have two Sar1 isoforms, Sar1a and Sar1b, that have approximately 90% sequence identity. Some experiments demonstrated that these two isoforms had distinct but overlapping functions. Here we found another instance of differing behavior: the alarmone ppGpp could bind to and inhibit the GTPase activity of human Sar1a but could not inhibit the GTPase activity of human Sar1b. The crystal structures of Sar1a⋅ppGpp and Sar1b⋅GDP have been determined. Superposition of the structures shows that ppGpp binds to the nucleotide-binding pocket, its guanosine base, ribose ring and 5'-diphosphate occupying nearly the same positions as for GDP. However, its 3'-diphosphate points away from the active site and, hence, away from the surface of the protein. The overall structure of Sar1a⋅ppGpp is more similar to Sar1b⋅GDP than to Sar1b⋅GTP. We also find that the Asp140-Arg138-water-ligand interaction net is important for the binding of ppGpp to Sar1a. This study provides further evidence showing that there are biochemical differences between the Sar1a and Sar1b isoforms of Sar1. PubMed: 36369712DOI: 10.1002/prot.26445 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.981 Å) |
Structure validation
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