Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 17 |
GO:0006979 | response to oxidative stress | 3 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0033554 | cellular response to stress | 3 | 17 |
GO:0034599 | cellular response to oxidative stress | 4 | 17 |
GO:0042221 | response to chemical | 2 | 17 |
GO:0050896 | response to stimulus | 1 | 17 |
GO:0051716 | cellular response to stimulus | 2 | 17 |
GO:0062197 | cellular response to chemical stress | 4 | 17 |
GO:0070887 | cellular response to chemical stimulus | 3 | 17 |
GO:0000302 | response to reactive oxygen species | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0010941 | regulation of cell death | 4 | 1 |
GO:0030322 | stabilization of membrane potential | 4 | 1 |
GO:0042391 | regulation of membrane potential | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0042743 | hydrogen peroxide metabolic process | 4 | 2 |
GO:0042744 | hydrogen peroxide catabolic process | 4 | 2 |
GO:0042981 | regulation of apoptotic process | 6 | 1 |
GO:0043066 | negative regulation of apoptotic process | 7 | 1 |
GO:0043067 | regulation of programmed cell death | 5 | 1 |
GO:0043069 | negative regulation of programmed cell death | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0060548 | negative regulation of cell death | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0072593 | reactive oxygen species metabolic process | 3 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
GO:1901700 | response to oxygen-containing compound | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004601 | peroxidase activity | 2 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0016209 | antioxidant activity | 1 | 17 |
GO:0016491 | oxidoreductase activity | 2 | 17 |
GO:0016684 | oxidoreductase activity, acting on peroxide as acceptor | 3 | 17 |
GO:0020037 | heme binding | 4 | 17 |
GO:0046906 | tetrapyrrole binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0004129 | cytochrome-c oxidase activity | 4 | 1 |
GO:0004447 | iodide peroxidase activity | 4 | 1 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0008447 | L-ascorbate oxidase activity | 5 | 1 |
GO:0009055 | electron transfer activity | 3 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015078 | proton transmembrane transporter activity | 5 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0015453 | oxidoreduction-driven active transmembrane transporter activity | 5 | 1 |
GO:0016675 | oxidoreductase activity, acting on a heme group of donors | 3 | 1 |
GO:0016679 | oxidoreductase activity, acting on diphenols and related substances as donors | 3 | 1 |
GO:0016682 | oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor | 4 | 1 |
GO:0016688 | L-ascorbate peroxidase activity | 3 | 5 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
GO:0140905 | haloperoxidase activity | 3 | 1 |
GO:0140906 | halogenase activity | 4 | 1 |
GO:0140825 | lactoperoxidase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.190 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.719 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.425 |
DEG_APCC_KENBOX_2 | 319 | 323 | PF00400 | 0.210 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.602 |
DEG_SPOP_SBC_1 | 38 | 42 | PF00917 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.333 |
DOC_PP1_RVXF_1 | 132 | 138 | PF00149 | 0.277 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.252 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.243 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.395 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.183 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.416 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.402 |
LIG_APCC_ABBAyCdc20_2 | 379 | 385 | PF00400 | 0.319 |
LIG_BIR_III_2 | 214 | 218 | PF00653 | 0.247 |
LIG_deltaCOP1_diTrp_1 | 204 | 208 | PF00928 | 0.231 |
LIG_deltaCOP1_diTrp_1 | 357 | 365 | PF00928 | 0.281 |
LIG_EH1_1 | 229 | 237 | PF00400 | 0.198 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.280 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.289 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.252 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.310 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.255 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.316 |
LIG_IBAR_NPY_1 | 67 | 69 | PF08397 | 0.420 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 196 | 203 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 367 | 377 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.337 |
LIG_LIR_LC3C_4 | 349 | 352 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 346 | 350 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.340 |
LIG_Pex14_1 | 361 | 365 | PF04695 | 0.270 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.297 |
LIG_PTB_Apo_2 | 277 | 284 | PF02174 | 0.277 |
LIG_PTB_Phospho_1 | 277 | 283 | PF10480 | 0.248 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.238 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.292 |
LIG_SH3_1 | 219 | 225 | PF00018 | 0.349 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.348 |
LIG_SUMO_SIM_anti_2 | 246 | 252 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 337 | 343 | PF11976 | 0.353 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.288 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.395 |
MOD_CDK_SPK_2 | 213 | 218 | PF00069 | 0.183 |
MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.183 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.239 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.183 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.369 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.262 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.446 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.292 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.401 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.255 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.302 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.218 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.373 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.533 |
MOD_Cter_Amidation | 58 | 61 | PF01082 | 0.712 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.383 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.282 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.247 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.512 |
MOD_GlcNHglycan | 261 | 266 | PF01048 | 0.469 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.465 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.459 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.477 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.246 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.333 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.235 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.397 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.269 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.455 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.364 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.516 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.325 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.383 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.435 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.447 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.452 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.252 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.338 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.355 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.548 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.577 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.281 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.309 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.255 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.338 |
MOD_PK_1 | 228 | 234 | PF00069 | 0.317 |
MOD_PKA_1 | 60 | 66 | PF00069 | 0.497 |
MOD_PKB_1 | 379 | 387 | PF00069 | 0.409 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.362 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.183 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.272 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.252 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.404 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.183 |
MOD_SUMO_rev_2 | 99 | 105 | PF00179 | 0.652 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.267 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.228 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 43 | 46 | PF00400 | 0.370 |
TRG_NLS_Bipartite_1 | 362 | 382 | PF00514 | 0.228 |
TRG_NLS_MonoExtN_4 | 326 | 332 | PF00514 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Y9 | Leptomonas seymouri | 76% | 96% |
A0A0S4JPM4 | Bodo saltans | 48% | 78% |
A0A1X0NHV6 | Trypanosomatidae | 54% | 100% |
A0A3S7WWR4 | Leishmania donovani | 89% | 100% |
A0A422N895 | Trypanosoma rangeli | 52% | 100% |
A4HAD2 | Leishmania braziliensis | 27% | 100% |
A4HZF3 | Leishmania infantum | 88% | 100% |
A4I9H5 | Leishmania infantum | 25% | 100% |
D0A114 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AVE9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B4H3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
H6V7N3 | Leishmania donovani | 25% | 100% |
Q4Q3K2 | Leishmania major | 25% | 100% |
Q4QC30 | Leishmania major | 86% | 100% |
V5BHD3 | Trypanosoma cruzi | 55% | 100% |