EC Number |
Recommended Name |
Source Tissue |
Reference |
---|
3.1.1.13 | sterol esterase |
macrophage |
- |
665963, 677459, 681075, 715834 |
1.13.11.52 | indoleamine 2,3-dioxygenase |
macrophage |
- |
666461, 711952, 743358 |
3.5.3.15 | protein-arginine deiminase |
macrophage |
- |
666904, 711811 |
3.5.3.1 | arginase |
macrophage |
alveolar macrophage |
667160, 686562 |
1.1.1.271 | GDP-L-fucose synthase |
macrophage |
- |
667231 |
2.7.7.30 | fucose-1-phosphate guanylyltransferase |
macrophage |
- |
667231 |
3.4.21.26 | prolyl oligopeptidase |
macrophage |
resident and elicited macrophage |
667550 |
3.4.24.B7 | matrix metalloproteinase-26 |
macrophage |
matrix metalloproteinase-26 is associated with macrophages and polymorphonuclear leukocytes |
668149 |
3.4.22.56 | caspase-3 |
macrophage |
from arteriosclerotic carotid artery, presence of proapoptotic markers such as enzyme, poly(ADP-ribose) polymerase, apoptosis-inducing factor, c-Jun/AP-1, and proinflammatory markers such as macrophage migration inhibitory factor and cyclooxygenase-2. Colocalization of proapoptic markers and proinflammatory markers and oxidized low-density lipoproteins |
668206 |
1.1.1.21 | aldose reductase |
macrophage |
in inflamed temporal arteries |
668868 |
3.4.22.27 | cathepsin S |
macrophage |
- |
667984, 668394, 668898, 679696, 680995, 682236, 695946, 696630, 696638, 696641, 696743, 697361, 698859, 699142, 699442, 701151, 701183, 753968 |
3.4.24.65 | macrophage elastase |
macrophage |
- |
-, 668953, 671345, 683327, 708303, 708422, 754337, 754734, 754996 |
3.4.22.15 | cathepsin L |
macrophage |
the maturation of cathepsin L is impaired in bone marrow-derived macrophages infected with Mycobacterium avium or Mycobacterium tuberculosis |
668959 |
3.4.22.41 | cathepsin F |
macrophage |
monocyte-derived cell culture, enzyme is secreted |
669249 |
3.4.22.43 | cathepsin V |
macrophage |
in plaque areas of diseased blood vessels, cathepsin expression levels during differentiation, overview |
669257 |
3.4.24.B11 | ADAMTS1 endopeptidase |
macrophage |
- |
669350, 755146 |
1.1.1.21 | aldose reductase |
macrophage |
- |
-, 669503, 738833, 739113 |
3.4.21.35 | tissue kallikrein |
macrophage |
- |
669519, 731671 |
3.4.24.63 | meprin B |
macrophage |
cortical and medullary macrophages of lymph node |
669708 |
3.4.24.B5 | matrix metalloproteinase-15 |
macrophage |
small expression |
669713 |
3.1.4.53 | 3',5'-cyclic-AMP phosphodiesterase |
macrophage |
PDE4B. Ablation of PDE4B partially protects mice from LPS-induced shock |
669723 |
1.1.1.146 | 11beta-hydroxysteroid dehydrogenase |
macrophage |
activity occurs after differentiation of neutrophils to macrophages |
669730 |
1.1.1.146 | 11beta-hydroxysteroid dehydrogenase |
macrophage |
derived from bone-marrow, peritoneal macrophages, expression of isozyme 11beta-HSD1, not isozyme 11beta-HSD2 |
669730 |
5.6.1.3 | plus-end-directed kinesin ATPase |
macrophage |
- |
670212 |
3.4.17.12 | carboxypeptidase M |
macrophage |
- |
670291 |
3.5.3.1 | arginase |
macrophage |
cultured head-kidney derived macrophages, significant enzyme activity, inhibitable by Nomega-hydroxy-L-arginine and induced by dibutyryl cyclic adenosine |
670294 |
3.5.3.1 | arginase |
macrophage |
cultured head-kidney derived macrophages, significant enzyme activity, inhibitable by Nomega-hydroxy-L-arginine, not inducible by dibutyryl cyclic adenosine |
670294 |
3.4.22.36 | caspase-1 |
macrophage |
bone-marrow derived |
670356 |
3.4.17.20 | Carboxypeptidase U |
macrophage |
- |
670940 |
2.7.10.2 | non-specific protein-tyrosine kinase |
macrophage |
- |
490151, 671253, 672781, 675097, 691455, 692647 |
3.4.24.65 | macrophage elastase |
macrophage |
specific for |
671345 |
2.8.1.7 | cysteine desulfurase |
macrophage |
enzyme isoform Nfs1 |
671626 |
2.8.1.7 | cysteine desulfurase |
macrophage |
mitochondrial isoform of Nfs1 |
671626 |
1.14.13.39 | nitric-oxide synthase (NADPH) |
macrophage |
inducible enzyme |
671728 |
1.15.1.1 | superoxide dismutase |
macrophage |
peritoneal macrophages exposed to He-Ne laser radiation. Changes in the activity of superoxide dismutase as well as the formation of nitric oxide and peroxynitrite depend to a large extent on the laser radiation dose. Activation of enzyme at low radiation doses is accompanied by nitric oxide level increase without changes in peroxynitrite. Enhanced laser radiation doses inhibit the enzyme |
672292 |
2.4.2.31 | NAD+-protein-arginine ADP-ribosyltransferase |
macrophage |
- |
672357 |
2.7.11.15 | beta-adrenergic-receptor kinase |
macrophage |
- |
-, 673187 |
1.6.5.2 | NAD(P)H dehydrogenase (quinone) |
macrophage |
enzyme is highly upregulated in active and chronic multiple sclerosis lesions, particularly in hypertrophic astrocytes and myelin-laden macrophages |
673798 |
2.7.11.16 | G-protein-coupled receptor kinase |
macrophage |
- |
674691 |
2.7.1.137 | phosphatidylinositol 3-kinase |
macrophage |
the regulatory subunit p87PIKAP and the catalytic subunit p101 are both expressed |
674783 |
2.7.1.91 | sphingosine kinase |
macrophage |
- |
674843 |
2.7.10.2 | non-specific protein-tyrosine kinase |
macrophage |
peritoneal and alveolar |
675097 |
2.7.1.107 | diacylglycerol kinase (ATP) |
macrophage |
- |
675157 |
2.7.10.2 | non-specific protein-tyrosine kinase |
macrophage |
peritoneal and splenic, and bone-marrow macrophages |
-, 675204 |
2.3.1.26 | sterol O-acyltransferase |
macrophage |
loss of ACAT activity in macrophages, either by pharmacological inhibition or by genetic knockout of ACAT-1, results in reduced induction of apoptosis in response to 7-ketocholesterol or oxidized low density lipoproteins. The apoptotic signal generated in macrophages by ACAT may be an arachidonyl oxysterol |
675261 |
3.4.21.B26 | proprotein convertase 5 |
macrophage |
- |
675490 |
1.14.15.18 | calcidiol 1-monooxygenase |
macrophage |
- |
675057, 675686 |
3.4.22.51 | cruzipain |
macrophage |
studies are carried out using murine macrophage cell line J774 as well as bone marrow-derived macrophages from BALB/c mice |
677418 |
3.1.4.3 | phospholipase C |
macrophage |
alveolar macrophage |
677502 |
3.4.23.34 | cathepsin E |
macrophage |
- |
677973, 679774 |
3.4.23.34 | cathepsin E |
macrophage |
mature form of CE in the endosomal structure |
678531 |
3.5.1.98 | histone deacetylase |
macrophage |
- |
678911 |
3.1.4.3 | phospholipase C |
macrophage |
monocyte-derived macrophage, enzyme is activated by HIV-1 R5 gp120 interaction with CCR5 and is required for NF-kB-mediated chemokine CCL2 production triggered by R5 gp120 |
678920 |
3.4.21.79 | granzyme B |
macrophage |
- |
-, 679007, 731617, 754761 |
3.4.18.1 | cathepsin X |
macrophage |
tumor-associated |
679023 |
3.4.22.1 | cathepsin B |
macrophage |
- |
679023, 709347 |
5.3.99.2 | Prostaglandin-D synthase |
macrophage |
of gut mucosa |
679038 |
3.4.22.36 | caspase-1 |
macrophage |
- |
-, 679079, 681017, 681030, 697733, 698235, 700198, 700362, 700983, 708709, 708712, 717941, 718077 |
3.4.22.36 | caspase-1 |
macrophage |
caspase-1-mediated macrophage necrosis is the source of the cytokine storm and rapid disease progression in anthrax lethal toxin-treated BALB/c mice |
679097 |
3.4.24.82 | ADAMTS-4 endopeptidase |
macrophage |
- |
677894, 679302 |
5.6.2.2 | DNA topoisomerase (ATP-hydrolysing) |
macrophage |
- |
679700 |
3.1.4.12 | sphingomyelin phosphodiesterase |
macrophage |
peritoneal |
680143 |
3.4.19.3 | pyroglutamyl-peptidase I |
macrophage |
- |
680172 |
3.4.15.1 | peptidyl-dipeptidase A |
macrophage |
mice with expression of angiotensin convertzing enzyme only in monocytes and macrophages have a marked resistance to the growth of melanoma due to an enhanced immune response |
680175 |
3.4.23.5 | cathepsin D |
macrophage |
comparative transcriptome analysis is carried out in cholesterol-loaded monocyte-derived macrophages from low high density lipoprotein cholesterol (HDL-C) patients and control group: expression of CTSD is reduced by 50% in monocyte-derived macrophages of low HDL subjects, most significantly those with cholesterol efflux defects but without mutation in ABCA1 groups as compared with controls |
680732 |
3.1.4.4 | phospholipase D |
macrophage |
adhesion of primary neutrophils and monocyte-derived macrohages to fibronectin is accompanied by marked stimulation of enzyme activity. Similarly, adhesion of myeloid-macrophage cell lines to fibronectin, collagen, or plastic results in significant activation. Stimulation of enzyme is rapid and persists for at least 90 min |
681193 |
3.4.22.36 | caspase-1 |
macrophage |
IFN regulatory factor IRF-2(-/-) macrophages exhibit increased basal and gliotoxin-induced caspase-1 mRNA expression and enhanced caspase-1 activity |
681202 |
5.3.99.2 | Prostaglandin-D synthase |
macrophage |
bone-marrow derived macrophage, lung and alveolar macrophage. Treatment with Escherichia coli lipopolysaccharide or Pseudomonas induce enzyme expression. Induction is regulated positively by AP-1 and negatively by p53 |
681206 |
3.4.23.34 | cathepsin E |
macrophage |
derived from mouse bone marrow precursors |
681209 |
3.1.1.47 | 1-alkyl-2-acetylglycerophosphocholine esterase |
macrophage |
no significant modifications of pPAF-AH mRNA in macrophages or in ApoB100 values is observed in hepatitis C virus patients compared with controls |
681670 |
3.4.22.36 | caspase-1 |
macrophage |
the Gram-negative bacterium Shigella flexneri triggers pro-inflammatory apoptotic cell death in macrophages, which is crucial for the onset of an acute inflammatory diarrhoea termed bacillary dysentery. The Mxi-Spa type III secretion system promotes bacterial uptake and escape into the cytoplasm, where, dependent on the translocator/effector protein IpaB, caspase-1 and its substrate IL-1b are activated |
681799 |
3.1.2.2 | palmitoyl-CoA hydrolase |
macrophage |
up-regulated by lipopolysaccharide and that overexpression of Acot7 in a macrophage cell line alters the production of prostaglandins D2 and E2 |
682542 |
3.4.22.36 | caspase-1 |
macrophage |
bone marrow derived. Anthrax lethal toxin and Salmonella elicit the common cell death pathway of caspase-1-dependent pyroptosis via distinct mechanisms. Activation of caspase-1 by Bacillus anthracis lethal toxin requires binding, uptake, and endosome acidification to mediate translocation of lethal factor into the host cell cytosol. Catalytically active lethal factor cleaves cytosolic substrates and activates caspase-1 by a mechanism involving proteasome activity and potassium efflux. Lethal toxin activation of caspase-1 requires the inflammasome adapter Nalp1. Salmonella infection activates caspase-1 through an independent pathway requiring the inflammasome adapter Ipaf. These distinct mechanisms of caspase-1 activation converge on a common pathway of caspase-1-dependent cell death featuring DNA cleavage, cytokine activation, and, ultimately, cell lysis resulting from the formation of membrane pores between 1.1 and 2.4 nm in diameter and pathological ion fluxes that can be blocked by glycine |
682588 |
3.2.1.52 | beta-N-acetylhexosaminidase |
macrophage |
the importance of beta-hexosaminidase for restricting mycobacterial growth during mammalian infections is confirmed in macrophages from beta-hexosaminidase knockout mice. beta-Hexosaminidase is characterized as a peptidoglycan hydrolase that exerts its mycobactericidal effect at the macrophage plasma membrane during mycobacteria-induced secretion of lysosomes |
682592 |
2.7.11.25 | mitogen-activated protein kinase kinase kinase |
macrophage |
TPL-2 and MEKK1 |
682954 |
3.2.2.5 | NAD+ glycohydrolase |
macrophage |
from bone marrow. Tumor necrosis factor alpha upregulates CD38. Induced CD38 expression enhances inflammatory gene expression by decreasing ERK1/2 phosphorylation and increasing NF kappaB activation. It negatively affects the expression of osteoclast markers. CD38 may reduce osteoclastogenesis and increase inflammatory gene induction by decreasing cellular histone deacetylase activity |
683052 |
3.4.24.65 | macrophage elastase |
macrophage |
alveolar |
-, 683054, 708452, 709559, 752886 |
3.4.21.6 | coagulation factor Xa |
macrophage |
high expression level in bronchoalveolar lavage fluid macrophages from asthmatic mice |
683057 |
3.4.22.41 | cathepsin F |
macrophage |
derived from cultured monocytes |
683112 |
3.4.22.34 | Legumain |
macrophage |
M-CSF differentiated primary macrophages, in vitro expression, also detected in the culture media |
683113 |
3.4.22.34 | Legumain |
macrophage |
of atherosclerotic aorta of aging Apolipoprotein E deficient mice, mRNA expression increases with development of atherosclerosis |
683113 |
3.4.24.23 | matrilysin |
macrophage |
- |
683356 |
3.4.24.71 | endothelin-converting enzyme 1 |
macrophage |
from blood, determination of enzyme expression by immunohistochemical analysis using a combination of ECE-1 isoform-specific antibodies, expression of isozymes ECE-1a and ECE-1c |
683440 |
3.4.21.109 | matriptase |
macrophage |
- |
683489, 695463, 698077 |
3.4.24.35 | gelatinase B |
macrophage |
secretion of MMP-9 in the early phase of peritonitis, no MMP-9 production in unstimulated macrophages |
-, 683525 |
3.4.21.73 | u-Plasminogen activator |
macrophage |
- |
-, 683623, 683741, 707951 |
3.4.21.73 | u-Plasminogen activator |
macrophage |
from bone-marrow |
683623 |
3.4.17.22 | metallocarboxypeptidase D |
macrophage |
- |
683703 |
3.4.24.35 | gelatinase B |
macrophage |
activated, MMP-9 secretion |
-, 683733 |
3.4.24.35 | gelatinase B |
macrophage |
secretion of MMP-9, transcription factor NF-kappaB is important in MMP gene regulation in macrophage cells |
683749 |
3.4.24.65 | macrophage elastase |
macrophage |
MMP-12 is secreted by macrophages at sites of inflammation |
683781 |
3.4.24.35 | gelatinase B |
macrophage |
- |
-, 684007, 707043, 708724, 709413, 709572, 709950, 733303, 733959 |
1.13.11.33 | arachidonate 15-lipoxygenase |
macrophage |
peritoneal |
-, 684350 |
3.5.3.1 | arginase |
macrophage |
- |
684384, 688998, 689301 |
3.4.21.7 | plasmin |
macrophage |
plasmin triggers expression and release of proinflammatory cytokines such as TNF-alpha and IL-6 in human monocyte-derived macrophages with a somewhat lower potency than the standard stimulus lipopolysaccharide. Plasmin-induced activation of JAK1, p38, ERK1/2, and NF-kappaB is indispensable for the cytokine expression |
684778 |
2.3.1.26 | sterol O-acyltransferase |
macrophage |
monocyte-derived macrophage |
684780 |
3.4.21.B1 | hyaluronan-binding serine protease |
macrophage |
highly expressed in macrophages of atherosclerotic lesions |
684801 |
1.13.11.31 | arachidonate 12-lipoxygenase |
macrophage |
peritoneal |
-, 684803 |
2.7.7.96 | ADP-D-ribose pyrophosphorylase |
macrophage |
- |
684834 |
1.15.1.1 | superoxide dismutase |
macrophage |
- |
685864 |