Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005838 | proteasome regulatory particle | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0000502 | proteasome complex | 3 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0008541 | proteasome regulatory particle, lid subcomplex | 2 | 1 |
GO:0031595 | nuclear proteasome complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
GO:1905369 | endopeptidase complex | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7WWF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.386 |
CLV_MEL_PAP_1 | 339 | 345 | PF00089 | 0.501 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.230 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.410 |
CLV_PCSK_PC7_1 | 385 | 391 | PF00082 | 0.313 |
CLV_Separin_Metazoa | 233 | 237 | PF03568 | 0.336 |
CLV_Separin_Metazoa | 73 | 77 | PF03568 | 0.462 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.399 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.411 |
DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.385 |
DOC_MAPK_gen_1 | 389 | 397 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 418 | 428 | PF00069 | 0.411 |
DOC_SPAK_OSR1_1 | 149 | 153 | PF12202 | 0.335 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.368 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 163 | 171 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 431 | 441 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.446 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_Clathr_ClatBox_1 | 425 | 429 | PF01394 | 0.421 |
LIG_Clathr_ClatBox_1 | 51 | 55 | PF01394 | 0.322 |
LIG_Clathr_ClatBox_1 | 69 | 73 | PF01394 | 0.187 |
LIG_deltaCOP1_diTrp_1 | 3 | 11 | PF00928 | 0.529 |
LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.363 |
LIG_FAT_LD_1 | 84 | 92 | PF03623 | 0.489 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.458 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.473 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.440 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.487 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.433 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.381 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.471 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.511 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.441 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.461 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.450 |
LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 414 | 422 | PF02991 | 0.442 |
LIG_LIR_LC3C_4 | 423 | 427 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.318 |
LIG_MYND_1 | 355 | 359 | PF01753 | 0.516 |
LIG_MYND_3 | 182 | 186 | PF01753 | 0.450 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.338 |
LIG_PCNA_yPIPBox_3 | 76 | 88 | PF02747 | 0.356 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.315 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.480 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.394 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.503 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.473 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.311 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.453 |
LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.362 |
LIG_SUMO_SIM_anti_2 | 344 | 351 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 375 | 380 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 448 | 453 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 31 | 40 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 50 | 55 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 66 | 73 | PF11976 | 0.342 |
LIG_SxIP_EBH_1 | 27 | 39 | PF03271 | 0.469 |
LIG_SxIP_EBH_1 | 379 | 390 | PF03271 | 0.513 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.324 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.340 |
LIG_UBA3_1 | 406 | 413 | PF00899 | 0.435 |
LIG_UBA3_1 | 464 | 472 | PF00899 | 0.545 |
LIG_UBA3_1 | 51 | 56 | PF00899 | 0.330 |
LIG_UBA3_1 | 87 | 96 | PF00899 | 0.448 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.491 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.404 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.437 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.466 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.433 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.520 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.453 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.436 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.468 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.499 |
MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.454 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.346 |
MOD_GlcNHglycan | 14 | 20 | PF01048 | 0.570 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.414 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.432 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.503 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.513 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.397 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.517 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.445 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.433 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.515 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.313 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.420 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.427 |
MOD_N-GLC_2 | 369 | 371 | PF02516 | 0.313 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.426 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.440 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.469 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.429 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.480 |
MOD_PK_1 | 332 | 338 | PF00069 | 0.369 |
MOD_PKA_1 | 163 | 169 | PF00069 | 0.486 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.518 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.457 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.463 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.414 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.438 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.516 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.436 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.398 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.478 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.402 |
MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.466 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.397 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.434 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.411 |
MOD_SUMO_rev_2 | 261 | 267 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 3 | 9 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.551 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.411 |
TRG_NES_CRM1_1 | 189 | 205 | PF08389 | 0.326 |
TRG_NES_CRM1_1 | 337 | 352 | PF08389 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 172 | 177 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 389 | 393 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAV3 | Leptomonas seymouri | 90% | 100% |
A0A0S4IPZ2 | Bodo saltans | 51% | 96% |
A0A1X0NY92 | Trypanosomatidae | 67% | 99% |
A0A422NHB9 | Trypanosoma rangeli | 67% | 99% |
A4HBS3 | Leishmania braziliensis | 95% | 100% |
A4HZ77 | Leishmania infantum | 100% | 100% |
D0A1G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 98% |
E9AV44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
O00232 | Homo sapiens | 30% | 100% |
P0CU17 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
P0CU18 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q12250 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q2KJ25 | Bos taurus | 31% | 100% |
Q4QCD7 | Leishmania major | 99% | 100% |
Q54UJ0 | Dictyostelium discoideum | 30% | 100% |
Q5RBI3 | Pongo abelii | 30% | 100% |
Q8VWK0 | Arabidopsis thaliana | 29% | 100% |
Q9D8W5 | Mus musculus | 31% | 100% |
Q9FIB6 | Arabidopsis thaliana | 29% | 100% |
V5BDS8 | Trypanosoma cruzi | 65% | 66% |