Search Results

Overview

Uniprot IDP21980
Protein NameProtein-glutamine gamma-glutamyltransferase 2
Gene NameTGM2
OrganismHomo 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

10 MAEELVLERC 20 DLELETNGRD 30 HHTADLCREK 40 LVVRRGQPFW 50 LTLHFEGRNY 60 EASVDSLTFS 70 VVTGPAPSQE 80 AGTKARFPLR 90 DAVEEGDWTA 100 TVVDQQDCTL 110 SLQLTTPANA 120 PIGLYRLSLE 130 ASTGYQGSSF 140 VLGHFILLFN 150 AWCPADAVYL 160 DSEEERQEYV 170 LTQQGFIYQG 180 SAKFIKNIPW 190 NFGQFEDGIL 200 DICLILLDVN 210 PKFLKNAGRD 220 CSRRSSPVYV 230 GRVVSGMVNC 240 NDDQGVLLGR 250 WDNNYGDGVS 260 PMSWIGSVDI 270 LRRWKNHGCQ 280 RVKYGQCWVF 290 AAVACTVLRC 300 LGIPTRVVTN 310 YNSAHDQNSN 320 LLIEYFRNEF 330 GEIQGDKSEM 340 IWNFHCWVES 350 WMTRPDLQPG 360 YEGWQALDPT 370 PQEKSEGTYC 380 CGPVPVRAIK 390 EGDLSTKYDA 400 PFVFAEVNAD 410 VVDWIQQDDG 420 SVHKSINRSL 430 IVGLKISTKS 440 VGRDEREDIT 450 HTYKYPEGSS 460 EEREAFTRAN 470 HLNKLAEKEE 480 TGMAMRIRVG 490 QSMNMGSDFD 500 VFAHITNNTA 510 EEYVCRLLLC 520 ARTVSYNGIL 530 GPECGTKYLL 540 NLNLEPFSEK 550 SVPLCILYEK 560 YRDCLTESNL 570 IKVRALLVEP 580 VINSYLLAER 590 DLYLENPEIK 600 IRILGEPKQK 610 RKLVAEVSLQ 620 NPLPVALEGC 630 TFTVEGAGLT 640 EEQKTVEIPD 650 PVEAGEEVKV 660 RMDLLPLHMG 670 LHKLVVNFES 680 DKLKAVKGFR NVIIGPA

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.