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CATHB1 | Cathepsin B-like protease 1; Thiol protease that plays a central role in plant programmed cell death (PCD). In addition to its role in protein degradation, may cleave and/or degrade a number of target proteins, activating signaling towards PCD. Contributes to the increase of caspase-3-like activity after UV-C-induced PCD and is required for abiotic stress-induced PCD. Functions redundantly with CATHB2 and CATHB3 in basal defense and distinct forms of plant programmed cell death (PCD). Participates to the establishment of basal resistance against the bacterial pathogen Pseudomonase syri [...] (379 aa) | ||||
RDL6 | Probable cysteine protease RDL6; Probable thiol protease. (356 aa) | ||||
UCH2 | Ubiquitin carboxyl-terminal hydrolase 2; Ubiquitin-protein hydrolase involved in the release of ubiquitin attached via both peptide and isopeptide linkages. Able to cleave 'Lys-48'-linked polyubiquitin chains. Involved in the direct or indirect regulation of AUX/IAA proteins stability. Acts as a linker between the TREX-2 complex and 26S proteasome ; Belongs to the peptidase C12 family. (330 aa) | ||||
UBP5 | Ubiquitin carboxyl-terminal hydrolase 5; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Belongs to the peptidase C19 family. (924 aa) | ||||
T14G11.20 | Cysteine proteinases superfamily protein; Belongs to the peptidase C1 family. (345 aa) | ||||
UBP3 | Ubiquitin carboxyl-terminal hydrolase 3; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Required for the correct development of pollen; Belongs to the peptidase C19 family. (371 aa) | ||||
AMC4 | Metacaspase-4 subunit p10; Cysteine protease that cleaves specifically after arginine or lysine residues. Does not cleave caspase-specific substrates. Plays a positive regulatory role in biotic and abiotic stress-induced programmed cell death. (418 aa) | ||||
AMC5 | Metacaspase-5; Cysteine protease that cleaves specifically after arginine or lysine residues. Does not cleave caspase-specific substrates. May be involved in the modulation of programmed cell death activated by oxidative stress. (410 aa) | ||||
AMC6 | Metacaspase-6; Belongs to the peptidase C14B family. (368 aa) | ||||
ULP1B | Putative ubiquitin-like-specific protease 1B; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. (341 aa) | ||||
XCP1 | Cysteine protease XCP1; Cysteine protease involved in xylem tracheary element (TE) autolysis during xylogenesis in roots. Participates in micro autolysis within the intact central vacuole before mega autolysis is initiated by tonoplast implosion. (355 aa) | ||||
RD19B | Probable cysteine protease RD19B; Probable thiol protease. (361 aa) | ||||
RD19A | Cysteine protease RD19A; Probable thiol protease (By similarity). Required for RRS1- mediated resistance against Ralstonia solanacearum. Plays a crucial role as host factor for PopP2-triggered RRS1-mediated resistance. Interacts with the R.solanacearum type III effector PopP2 to form a nuclear complex that is required for activation of the RRS1-mediated resistance response ; Belongs to the peptidase C1 family. (368 aa) | ||||
RD21A | Cysteine proteinase RD21A; Cysteine protease that plays a role in immunity, senescence, and biotic and abiotic stresses (Probable). Involved in immunity against the necrotrophic fungal pathogen Botrytis cinerea. Involved in elicitor-stimulated programmed cell death (PCD). During infection by the necrotrophic fungal pathogen Botrytis cinerea, functions as PCD-promoting protease that is released from the ER body or vacuole to the cytoplasm. Accumulates in endoplasmic reticulum-derived bodies in epidermal cells and may participate in cell death in stressed or injured cells. Involved in wa [...] (462 aa) | ||||
ALPHA-VPE | Vacuolar-processing enzyme alpha-isozyme; Asparagine-specific endopeptidase involved in the processing of vacuolar seed protein precursors into the mature forms. Probably involved in post-translational proteolysis of seed storage proteins in the protein storage vacuole of developing seeds. (478 aa) | ||||
ULP2A | Probable ubiquitin-like-specific protease 2A; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. (774 aa) | ||||
XBCP3 | Papain-like cysteine peptidase XBCP3; Belongs to the peptidase C1 family. (437 aa) | ||||
ULP1D | Ubiquitin-like-specific protease 1D; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. Cleaves precursors of SUM1 and SUM2, but not of SUM3 or SUM5. Able to release SUM1 and SUM2 from conjugates, but unable to cleave SUM3. Protease activity mainly directed at deconjugating SUM1 and SUM2 from their target proteins. Regulates salt stress responses and flowering time. Redundant with ULP1C. (584 aa) | ||||
bVPE | Vacuolar-processing enzyme beta-isozyme; Asparagine-specific endopeptidase involved in the processing of vacuolar seed protein precursors into the mature forms (By similarity). Probably involved in post-translational proteolysis of seed storage proteins in the protein storage vacuole of developing seeds. (486 aa) | ||||
GAMMA-VPE | Vacuolar-processing enzyme gamma-isozyme; Asparagine-specific endopeptidase involved in the processing of vacuolar seed protein precursors into the mature forms. Probably involved in post-translational proteolysis of seed storage proteins in the protein storage vacuole of developing seeds. (494 aa) | ||||
UBP18 | Ubiquitin carboxyl-terminal hydrolase 18; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). (631 aa) | ||||
AMC7 | Metacaspase-7; Belongs to the peptidase C14B family. (403 aa) | ||||
AMC2 | Metacaspase-2; Acts as a negative regulator of oxidative stress cell death and hypersensitive cell death response mediated by immune response. Acts via indirect or direct regulation of AMC1 at postranscriptional level; Belongs to the peptidase C14B family. (418 aa) | ||||
AMC1 | Metacaspase-1; Cysteine protease that cleaves specifically after arginine or lysine residues. Does not cleave caspase-specific substrates. Acts as a positive regulator of cell death. Required for both oxidative stress cell death response and hypersensitive cell death response mediated by immune response. (367 aa) | ||||
F28N24.20 | Cysteine proteinases superfamily protein; Belongs to the peptidase C1 family. (355 aa) | ||||
UBP7 | Ubiquitin carboxyl-terminal hydrolase 7; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). (477 aa) | ||||
UBP13 | Ubiquitin carboxyl-terminal hydrolase 13; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (1115 aa) | ||||
UCH3 | Ubiquitin carboxyl-terminal hydrolase 3. (234 aa) | ||||
ULP1A | Ubiquitin-like-specific protease 1A; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. Cleaves precursors of SUM1 and SUM2, and very inefficiently of SUM3. Seems to be the only ULP1 able to cleave SUM3 precursors. Cleaves SUMO peptides better than SUMO-conjugated proteins; Belongs to the peptidase C48 family. (502 aa) | ||||
ALEU | Thiol protease aleurain; May play a role in proteolysis leading to mobilization of nitrogen during senescence and starvation. (358 aa) | ||||
UBP14 | Ubiquitin carboxyl-terminal hydrolase 14; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Involved in seed and embryo development. (797 aa) | ||||
ULP2B | Probable ubiquitin-like-specific protease 2B; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins; Belongs to the peptidase C48 family. (931 aa) | ||||
UBP4 | Ubiquitin carboxyl-terminal hydrolase 4; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Required for the correct development of pollen. (365 aa) | ||||
OTU1 | OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 1; Hydrolase that can remove conjugated ubiquitin from proteins in vitro and may therefore play an important regulatory role at the level of protein turnover by preventing degradation. Cysteine protease with a preference for Met-1 and 'Lys-48' over 'Lys- 63'-linked ubiquitin (UB) tetramers (e.g. Ub2, Ub3 and Ub4) as substrates ; Belongs to the peptidase C65 family. (306 aa) | ||||
DEK1 | Calpain-type cysteine protease DEK1; Essential protease involved in epiderm development. Required for aleurone cell development in the endosperm probably by maintaining and restricting the aleurone and embryonic epidermal L1 cell-layer fates as well as meristems organization. Involved in the maintenance of adaxial/abaxial axis information in developing leaves, probably by regulating cell proliferation and expansion. Does not need calcium ions to be active. Required for the formation of giant cells in sepals by determining cell fate and promoting endoreplication. (2151 aa) | ||||
ULP1C | Ubiquitin-like-specific protease 1C; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. Cleaves precursors of SUM1 and SUM2, but not of SUM3 or SUM5. Able to release SUM1 and SUM2 from conjugates, but unable to cleave SUM3. Protease activity mainly directed at deconjugating SUM1 and SUM2 from their target proteins. Regulates salt stress responses and flowering time. Redundant with ULP1D. (571 aa) | ||||
F18N11.70 | Thiol protease aleurain-like. (358 aa) | ||||
ATG4A | Cysteine protease ATG4a; Cysteine protease required for autophagy, which is able to cleave the C-terminal part of ATG8 that may be subsequently converted to a smaller form, with a revealed C-terminal glycine. ATG8 is then activated by ATG7 and is subsequently attached to ATG3, another E2-like enzyme, after which the C-terminal glycine of ATG8 is conjugated to phosphatidylethanolamine by an amide bond. This conjugated form has the capacity for the binding to autophagosomes; Belongs to the peptidase C54 family. (467 aa) | ||||
RD19D | Probable cysteine protease RD19D; Probable thiol protease. (367 aa) | ||||
UBP2 | Ubiquitin carboxyl-terminal hydrolase 2; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Is involved in resistance to the arginine analog canavanine (CAN). Belongs to the peptidase C19 family. (961 aa) | ||||
CATHB2 | Cathepsin B-like protease 2; Thiol protease that plays a central role in plant programmed cell death (PCD). In addition to its role in protein degradation, may cleave and/or degrade a number of target proteins, activating signaling towards PCD. Contributes to the increase of caspase-3-like activity after UV-C-induced PCD and is required for abiotic stress-induced PCD. Functions redundantly with CATHB1 and CATHB3 in basal defense and distinct forms of plant programmed cell death (PCD). Participates to the establishment of basal resistance against the bacterial pathogen Pseudomonase syri [...] (362 aa) | ||||
UBP9 | Ubiquitin carboxyl-terminal hydrolase 9; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (910 aa) | ||||
UBP6 | Ubiquitin carboxyl-terminal hydrolase 6; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins; Belongs to the peptidase C19 family. (482 aa) | ||||
GCP1-2 | Germination-specific cysteine protease 1; Probable thiol protease. (376 aa) | ||||
ESD4 | Ubiquitin-like-specific protease ESD4; Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMOs to their mature forms and deconjugation of SUMO from targeted proteins. Cleaves precursors of SUM1 and SUM2, but not of SUM3 or SUM5. Able to release SUM1 and SUM2 from conjugates, but unable to cleave SUM3. Acts predominantly as an isopeptidase, cleaving SUMO-conjugated proteins better than SUMO peptides. Plays an important role in the control of flowering time. (489 aa) | ||||
CATHB3 | Cathepsin B-like protease 3; Thiol protease that possesses high activity toward the cathepsin synthetic substrate Arg-Arg-7-amino-4-methylcoumarin (RR-AMC) and the papain substrate Gly-Arg-Arg-AMC (GRR-AMC). Can cleave the papain substrate Phe-Arg-AMC (FR-AMC) and the caspase-3 substrate Asp- Glu-Val-Asp-rhodamine 110 (DEVD-R110). Has no activity towards the caspase-6 substrate VEID-AMC, caspase-8 substrate IETD-AMC and caspase- 1 substrate YVAD-AMC. Plays a central role in plant programmed cell death (PCD). In addition to its role in protein degradation, may cleave and/or degrade a nu [...] (359 aa) | ||||
UBP8 | Ubiquitin carboxyl-terminal hydrolase 8; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (871 aa) | ||||
UCH1 | Ubiquitin carboxyl-terminal hydrolase; Ubiquitin-protein hydrolase involved in the release of ubiquitin attached via both peptide and isopeptide linkages. Able to cleave 'Lys-48'-linked polyubiquitin chains. Involved in the direct or indirect regulation of AUX/IAA proteins stability (Probable). Acts as a linker between the TREX-2 complex and 26S proteasome. (334 aa) | ||||
CEP1-2 | KDEL-tailed cysteine endopeptidase CEP1; Possesses protease activity in vitro. Involved in the final stage of developmental programmed cell death and in intercalation of new cells. Cleaves extensins, thus probably supporting the final cell collapse. During the compatible interaction with the biotrophic powdery mildew fungus Erysiphe cruciferarum, involved in the control of late epidermal cell death that limits growth and susceptibility to the parasite. During anther development, involved in tapetal programmed cell death (PCD), leading to degeneration of tapetal cells and functional pol [...] (361 aa) | ||||
UBP21 | Ubiquitin carboxyl-terminal hydrolase 21; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (732 aa) | ||||
SAG12 | Senescence-specific cysteine protease SAG12; Cysteine protease that may have a developmental senescence specific cell death function during apoptosis, heavy metal detoxification, and hypersensitive response. (346 aa) | ||||
UBP17 | Ubiquitin carboxyl-terminal hydrolase 17; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (731 aa) | ||||
AMC3 | Metacaspase-3. (362 aa) | ||||
RD21B | Probable cysteine protease RD21B; Probable thiol protease. (463 aa) | ||||
UBP27 | Ubiquitin carboxyl-terminal hydrolase 27; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). (494 aa) | ||||
UBP25 | Ubiquitin carboxyl-terminal hydrolase 25; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (661 aa) | ||||
UBP24 | Ubiquitin carboxyl-terminal hydrolase 24; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (551 aa) | ||||
UBP23 | Ubiquitin carboxyl-terminal hydrolase 23; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (859 aa) | ||||
UBP20 | Ubiquitin carboxyl-terminal hydrolase 20; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (695 aa) | ||||
UBP15 | Ubiquitin carboxyl-terminal hydrolase 15; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (Probable). Involved in the regulation of organ size. Acts as positive regulator of cell proliferation. Possesses deubiquitinating enzyme activity in vitro. The enzyme activity of UBP15 is required for its function in regulation of cell proliferation. Functions antagonistically in a common pathway with DA1 to regulate seed size. Acts maternally to regulate seed size by p [...] (924 aa) | ||||
UBP12 | Ubiquitin carboxyl-terminal hydrolase 12; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). (1116 aa) | ||||
UBP1 | Ubiquitin carboxyl-terminal hydrolase 1; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Is involved in resistance to the arginine analog canavanine (CAN). Belongs to the peptidase C19 family. (1083 aa) | ||||
AMC9 | Metacaspase-9 subunit p10; Cysteine protease that cleaves specifically after arginine or lysine residues. Does not cleave caspase-specific substrates. Required for proteolytic processing of GRI. Belongs to the peptidase C14B family. (325 aa) | ||||
UBP22 | Ubiquitin C-terminal hydrolase 22; Component of a deubiquitination module (DUB module) that specifically deubiquinates monoubiquinated histone H2B (H2Bub). Does not seem to be a component of the TREX-2 complex. Seems to act independently of the SAGA multiprotein complex. The DUB module is responsible for the major H2Bub deubiquitinase activity in Arabidopsis ; Belongs to the peptidase C19 family. (557 aa) | ||||
dVPE | Vacuolar-processing enzyme delta-isozyme; Asparagine-specific endopeptidase that may be involved in processing of proteins targeted to vacuoles (By similarity). Probably involved in post-translational proteolysis of seed storage proteins in the protein storage vacuole of developing seeds. Exhibits a caspase-1-like activity in extracellular granules. At the early stage of seed development, required for the formation of the seed coat, by regulating cell death of specific cell layers in inner integument. (466 aa) | ||||
XCP2 | Cysteine protease XCP2; Cysteine protease involved in xylem tracheary element (TE) autolysis during xylogenesis in roots. Participates in micro autolysis within the intact central vacuole before mega autolysis is initiated by tonoplast implosion. Involved in susceptibility to the bacterial plant pathogen Ralstonia solanacearum. (356 aa) | ||||
F9P14.12 | Cysteine proteinases superfamily protein; Belongs to the peptidase C1 family. (343 aa) | ||||
F28N24.27 | Peptidase C1A papain family protein; Belongs to the peptidase C1 family. (346 aa) | ||||
OTU2 | OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 2; Hydrolase that can remove conjugated ubiquitin from proteins in vitro and may therefore play an important regulatory role at the level of protein turnover by preventing degradation. Cysteine protease with a preference for 'Lys-63' and 'Lys-48' -linked ubiquitin (UB) tetramers as substrates. Belongs to the peptidase C85 family. (208 aa) | ||||
NEDP1 | NEDD8-specific protease 1; Processes the pre-form of the ubiquitin-like protein NEDD8/RUB1. Has the capacity to discriminate between NEDD8/RUB1 and ubiquitin. Has no SUMO protease activity. (226 aa) | ||||
RDL2 | Probable cysteine protease RDL2; Probable thiol protease; Belongs to the peptidase C1 family. (362 aa) | ||||
RD21C | Probable cysteine protease RD21C; Probable thiol protease; Belongs to the peptidase C1 family. (452 aa) | ||||
RDL3 | Probable cysteine protease RDL3; Probable thiol protease. (376 aa) | ||||
OTU5 | OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 5; Hydrolase that can remove conjugated ubiquitin from proteins in vitro and may therefore play an important regulatory role at the level of protein turnover by preventing degradation (Probable). Inactive cysteine protease. Deubiquitinating enzyme which regulates gene expression by contributing to chromatin organization and DNA methylation patterns (e.g. H3K4me3 and H3K27me3). Involved in the interpretation of environmental information, probably by altering chromatin organization and maintaining redox homeostasis. Required for pho [...] (332 aa) | ||||
ATG4B | Cysteine protease ATG4b; Cysteine protease required for autophagy, which is able to cleave the C-terminal part of ATG8 that may be subsequently converted to a smaller form, with a revealed C-terminal glycine. ATG8 is then activated by ATG7 and is subsequently attached to ATG3, another E2-like enzyme, after which the C-terminal glycine of ATG8 is conjugated to phosphatidylethanolamine by an amide bond. This conjugated form has the capacity for the binding to autophagosomes. (477 aa) | ||||
F24B22.90 | Ataxin-3 homolog; Interacts with key regulators of transcription and represses transcription. Acts as a histone-binding protein that regulates transcription. Acts as a deubiquitinating enzyme (By similarity). (280 aa) | ||||
UBP11 | Putative ubiquitin carboxyl-terminal hydrolase 11; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (892 aa) | ||||
AMC8 | Metacaspase-8; Cysteine protease that cleaves specifically after arginine residues. Does not cleave caspase-specific substrates. May be involved in the modulation of programmed cell death activated by oxidative stress; Belongs to the peptidase C14B family. (381 aa) | ||||
UBP16 | Ubiquitin carboxyl-terminal hydrolase 16; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Involved in salt tolerance by modulating sodium transport activity and repressing cell death at least partially through modulating SHM1 stability and activity. Involved in cadmium tolerance by interacting with HIPP27 and probably modulating its stability. Belongs to the peptidase C19 family. (1008 aa) | ||||
UBP26 | Ubiquitin carboxyl-terminal hydrolase 26; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Deubiquitinates H2BK143ub1 of histone H2B; Belongs to the peptidase C19 family. (1067 aa) | ||||
T1G12.4 | Putative cysteine proteinase; 15366-14136; Belongs to the peptidase C1 family. (341 aa) | ||||
UBP19 | Ubiquitin carboxyl-terminal hydrolase 19; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (672 aa) | ||||
CEP2-2 | KDEL-tailed cysteine endopeptidase CEP2; Involved in the final stage of developmental programmed cell death and in intercalation of new cells. Cleaves extensins, thus probably supporting the final cell collapse. (361 aa) | ||||
CEP3-2 | KDEL-tailed cysteine endopeptidase CEP3; Involved in the final stage of developmental programmed cell death and in intercalation of new cells. Cleaves extensins, thus probably supporting the final cell collapse. Belongs to the peptidase C1 family. (364 aa) | ||||
T29H11.100 | Probable Ufm1-specific protease; Thiol protease which recognizes and hydrolyzes the peptide bond at the C-terminal Gly of UFM1, a ubiquitin-like modifier protein bound to a number of target proteins; Belongs to the peptidase C78 family. (645 aa) | ||||
RD19C | Probable cysteine protease RD19C; Probable thiol protease. (373 aa) | ||||
RDL5-2 | Probable cysteine protease RDL5; Possesses protease activity in vitro. (371 aa) | ||||
RDL4 | Probable cysteine protease RDL4; Probable thiol protease; Belongs to the peptidase C1 family. (364 aa) | ||||
F10A12.10 | Cysteine proteinases superfamily protein; Belongs to the peptidase C1 family. (348 aa) | ||||
UBP10 | Ubiquitin carboxyl-terminal hydrolase 10; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (923 aa) |