Loading the page.
Proteins/UNIPROT:Q9BVA6
Protein that can both mediate the addition of adenosine 5'-monophosphate (AMP) to specific residues of target proteins (AMPylation), and the removal of the same modification from target proteins (de-AMPylation), depending on the context (By similarity). The side chain of Glu-231 determines which of the two opposing activities (AMPylase or de-AMPylase) will take place. Acts as a key regulator of the ERN1/IRE1-mediated unfolded protein response (UPR) by mediating AMPylation or de-AMPylation of HSPA5/BiP. In unstressed cells, acts as an adenylyltransferase by mediating AMPylation of HSPA5/BiP at 'Thr-518', thereby inactivating it (By similarity). In response to endoplasmic reticulum stress, acts as a phosphodiesterase by mediating removal of ATP (de-AMPylation) from HSPA5/BiP at 'Thr-518', leading to restore HSPA5/BiP activity (By similarity). Although it is able to AMPylate RhoA, Rac and Cdc42 Rho GTPases in vitro, Rho GTPases do not constitute physiological substrates..
Function from UniProtKB (Q9BVA6), read 2026-09-23. CC BY 4.0.
Curated compounds routed: 0
1 row
14 statements
14 statements · 3 reference databases · Subject: FICD · Sources: gene ontology, Hetionet, UniProt
3 reactions
L-tyrosyl-[protein]+ATP(4-)O-(5'-adenylyl)-L-tyrosyl-[protein]+diphosphate(3-)
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:54288CC BY 4.0Reference data
L-threonyl-[protein]+ATP(4-)3-O-(5'-adenylyl)-L-threonyl-[protein]+diphosphate(3-)
Reaction pageLeft to rightBalance undeterminable
9 names
Resolves to: FICD
3-O-(5'-adenylyl)-L-threonyl-[protein]+waterL-threonyl-[protein]+AMP+hydron
Catalysed by FICD
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:55932CC BY 4.0Reference data