Search Results
Overview
| Uniprot ID | P21980 |
|---|---|
| Protein Name | Protein-glutamine gamma-glutamyltransferase 2 |
| Gene Name | TGM2 |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position | Flanking peptide |
|---|---|
| 205 | DVNPKFLKNAGRDCS |
| 380 | PVPVRAIKEGDLSTK |
| 429 | VGLKISTKSVGRDER |
| 464 | TRANHLNKLAEKEET |
| 468 | HLNKLAEKEETGMAM |
| 550 | PLCILYEKYRDCLTE |
| 562 | LTESNLIKVRALLVE |
| 590 | YLENPEIKIRILGEP |
| 598 | IRILGEPKQKRKLVA |
| 672 | VVNFESDKLKAVKGF |
| 674 | NFESDKLKAVKGFRN |
Function
Calcium-dependent acyltransferase that catalyzes the formation of covalent bonds between peptide-bound glutamine and various primary amines, such as gamma-amino group of peptide-bound lysine, or mono- and polyamines, thereby producing cross-linked or aminated proteins, respectively (PubMed:23941696, PubMed:31991788, PubMed:9252372). Involved in many biological processes, such as bone development, angiogenesis, wound healing, cellular differentiation, chromatin modification and apoptosis (PubMed:1683874, PubMed:27270573, PubMed:28198360, PubMed:7935379, PubMed:9252372). Acts as a protein-glutamine gamma-glutamyltransferase by mediating the cross-linking of proteins, such as ACO2, HSPB6, FN1, HMGB1, RAP1GDS1, SLC25A4/ANT1, SPP1 and WDR54 (PubMed:23941696, PubMed:24349085, PubMed:29618516, PubMed:30458214). Under physiological conditions, the protein cross-linking activity is inhibited by GTP; inhibition is relieved by Ca(2+) in response to various stresses (PubMed:18092889, PubMed:7592956, PubMed:7649299). When secreted, catalyzes cross-linking of proteins of the extracellular matrix, such as FN1 and SPP1 resulting in the formation of scaffolds (PubMed:12506096). Plays a key role during apoptosis, both by (1) promoting the cross-linking of cytoskeletal proteins resulting in condensation of the cytoplasm, and by (2) mediating cross-linking proteins of the extracellular matrix, resulting in the irreversible formation of scaffolds that stabilize the integrity of the dying cells before their clearance by phagocytosis, thereby preventing the leakage of harmful intracellular components (PubMed:7935379, PubMed:9252372). In addition to protein cross-linking, can use different monoamine substrates to catalyze a vast array of protein post-translational modifications: mediates aminylation of serotonin, dopamine, noradrenaline or histamine into glutamine residues of target proteins to generate protein serotonylation, dopaminylation, noradrenalinylation or histaminylation, respectively (PubMed:23797785, PubMed:30867594). Mediates protein serotonylation of small GTPases during activation and aggregation of platelets, leading to constitutive activation of these GTPases (By similarity). Plays a key role in chromatin organization by mediating serotonylation and dopaminylation of histone H3 (PubMed:30867594, PubMed:32273471). Catalyzes serotonylation of 'Gln-5' of histone H3 (H3Q5ser) during serotonergic neuron differentiation, thereby facilitating transcription (PubMed:30867594). Acts as a mediator of neurotransmission-independent role of nuclear dopamine in ventral tegmental area (VTA) neurons: catalyzes dopaminylation of 'Gln-5' of histone H3 (H3Q5dop), thereby regulating relapse-related transcriptional plasticity in the reward system (PubMed:32273471). Regulates vein remodeling by mediating serotonylation and subsequent inactivation of ATP2A2/SERCA2 (By similarity). Also acts as a protein deamidase by mediating the side chain deamidation of specific glutamine residues of proteins to glutamate (PubMed:20547769, PubMed:9623982). Catalyzes specific deamidation of protein gliadin, a component of wheat gluten in the diet (PubMed:9623982). May also act as an isopeptidase cleaving the previously formed cross-links (PubMed:26250429, PubMed:27131890). Also able to participate in signaling pathways independently of its acyltransferase activity: acts as a signal transducer in alpha-1 adrenergic receptor-mediated stimulation of phospholipase C-delta (PLCD) activity and is required for coupling alpha-1 adrenergic agonists to the stimulation of phosphoinositide lipid metabolism (PubMed:8943303)
Protein Sequence
Gene Ontology
| Classification | GO ID | Description |
|---|---|---|
| Cellular Component | GO:0000785 | chromatin |
| Cellular Component | GO:0005829 | cytosol |
| Cellular Component | GO:0005783 | endoplasmic reticulum |
| Cellular Component | GO:0070062 | extracellular exosome |
| Cellular Component | GO:0031012 | extracellular matrix |
| Cellular Component | GO:0005925 | focal adhesion |
| Cellular Component | GO:0005739 | mitochondrion |
| Cellular Component | GO:0000786 | nucleosome |
| Cellular Component | GO:0005634 | nucleus |
| Cellular Component | GO:0048471 | perinuclear region of cytoplasm |
| Cellular Component | GO:0005886 | plasma membrane |
| Molecular Function | GO:0005509 | calcium ion binding |
| Molecular Function | GO:0005525 | GTP binding |
| Molecular Function | GO:0005096 | GTPase activator activity |
| Molecular Function | GO:0120297 | histone dopaminyltransferase activity |
| Molecular Function | GO:0120295 | histone serotonyltransferase activity |
| Molecular Function | GO:0008233 | peptidase activity |
| Molecular Function | GO:0120299 | peptide histaminyltransferase activity |
| Molecular Function | GO:0120298 | peptide noradrenalinyltransferase activity |
| Molecular Function | GO:0003810 | protein-glutamine gamma-glutamyltransferase activity |
| Molecular Function | GO:0050568 | protein-glutamine glutaminase activity |
| Biological Process | GO:0043277 | apoptotic cell clearance |
| Biological Process | GO:0060348 | bone development |
| Biological Process | GO:0071314 | cellular response to cocaine |
| Biological Process | GO:1903351 | cellular response to dopamine |
| Biological Process | GO:1904015 | cellular response to serotonin |
| Biological Process | GO:0030198 | extracellular matrix organization |
| Biological Process | GO:0032471 | negative regulation of endoplasmic reticulum calcium ion concentration |
| Biological Process | GO:0018149 | peptide cross-linking |
| Biological Process | GO:0007200 | phospholipase C-activating G protein-coupled receptor signaling pathway |
| Biological Process | GO:0043065 | positive regulation of apoptotic process |
| Biological Process | GO:0045785 | positive regulation of cell adhesion |
| Biological Process | GO:0051561 | positive regulation of mitochondrial calcium ion concentration |
| Biological Process | GO:0050769 | positive regulation of neurogenesis |
| Biological Process | GO:0051057 | positive regulation of small GTPase mediated signal transduction |
| Biological Process | GO:1903672 | positive regulation of sprouting angiogenesis |
| Biological Process | GO:0051260 | protein homooligomerization |
| Biological Process | GO:0006508 | proteolysis |
| Biological Process | GO:2000425 | regulation of apoptotic cell clearance |
| Biological Process | GO:0042981 | regulation of apoptotic process |
Reference
[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.
[2] Hong H, Chen X, Wang H, Gu X, Yuan Y et al.. Global profiling of protein lysine lactylation and potential target modified protein analysis in hepatocellular carcinoma.. Proteomics 23(9):e2200432. 2023 May. PMID: 36625413.
[3] He J, Lai T, Zhou Z, Yang H, Lei Z et al.. Multiomics profiling reveals the involvement of protein lactylation in nonhomologous end joining pathway conferring radioresistance in lung adenocarcinoma cell.. Sci Rep 15(1):24651. 2025 Jul 9. PMID: 40634431.
[4] Wu Q, Li Z, Gong T, Zheng X, Zhou X et al.. Porphyromonas gingivalis infection induces lysine lactylation reprogramming in human umbilical vein endothelial cells.. Front Cell Infect Microbiol 16:1706727. 2026. PMID: 41696360.