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. | yes | yes: 10 |
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. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000502 | proteasome complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0140535 | intracellular protein-containing complex | 2 | 10 |
GO:1902494 | catalytic complex | 2 | 10 |
GO:1905368 | peptidase complex | 3 | 10 |
GO:1905369 | endopeptidase complex | 4 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0008541 | proteasome regulatory particle, lid subcomplex | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3D3
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:0005198 | structural molecule activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 503 | 507 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.255 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 526 | 532 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.255 |
CLV_Separin_Metazoa | 336 | 340 | PF03568 | 0.550 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.575 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.353 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.363 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.468 |
DEG_APCC_KENBOX_2 | 485 | 489 | PF00400 | 0.458 |
DEG_SCF_TRCP1_1 | 519 | 525 | PF00400 | 0.532 |
DOC_CYCLIN_RxL_1 | 25 | 34 | PF00134 | 0.501 |
DOC_CYCLIN_RxL_1 | 399 | 410 | PF00134 | 0.415 |
DOC_CYCLIN_RxL_1 | 89 | 99 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 254 | 262 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 168 | 176 | PF00069 | 0.330 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 92 | 96 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.550 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 199 | 206 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 25 | 32 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 342 | 358 | PF00022 | 0.511 |
LIG_Actin_WH2_2 | 380 | 396 | PF00022 | 0.511 |
LIG_APCC_ABBA_1 | 404 | 409 | PF00400 | 0.536 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.455 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.511 |
LIG_eIF4E_1 | 56 | 62 | PF01652 | 0.511 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.521 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.475 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.550 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.544 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.456 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.540 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.514 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.501 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 305 | 313 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.430 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.404 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.412 |
LIG_NRBOX | 57 | 63 | PF00104 | 0.485 |
LIG_NRP_CendR_1 | 530 | 532 | PF00754 | 0.536 |
LIG_PCNA_yPIPBox_3 | 455 | 468 | PF02747 | 0.577 |
LIG_Rb_pABgroove_1 | 456 | 464 | PF01858 | 0.448 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.401 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.435 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.337 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.455 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.455 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 426 | 429 | PF00017 | 0.676 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.675 |
LIG_SH2_PTP2 | 138 | 141 | PF00017 | 0.470 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.470 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.676 |
LIG_SH2_SRC | 444 | 447 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.675 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.497 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.550 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.529 |
LIG_SUMO_SIM_par_1 | 11 | 18 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 166 | 173 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.486 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.473 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.337 |
LIG_UBA3_1 | 307 | 314 | PF00899 | 0.368 |
LIG_UBA3_1 | 461 | 468 | PF00899 | 0.463 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.423 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.499 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.424 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.460 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.332 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.504 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.456 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.428 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.370 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.212 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.333 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.510 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.496 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.497 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.345 |
MOD_GlcNHglycan | 320 | 324 | PF01048 | 0.353 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.728 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.417 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.561 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.449 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.434 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.408 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.312 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.404 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.409 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.437 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.308 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.412 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.504 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.302 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.423 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.506 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.370 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.410 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.507 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.411 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.389 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.431 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.527 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.379 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.313 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.322 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.489 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.419 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.435 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.423 |
MOD_SUMO_rev_2 | 173 | 181 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 225 | 232 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 376 | 385 | PF00179 | 0.352 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_2 | 124 | 130 | PF01217 | 0.308 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.339 |
TRG_NES_CRM1_1 | 30 | 46 | PF08389 | 0.354 |
TRG_NES_CRM1_1 | 365 | 376 | PF08389 | 0.308 |
TRG_NLS_MonoExtC_3 | 493 | 498 | PF00514 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3L4 | Leptomonas seymouri | 77% | 100% |
A0A0S4JHD2 | Bodo saltans | 55% | 100% |
A0A1X0NKK6 | Trypanosomatidae | 59% | 94% |
A0A3R7KIY0 | Trypanosoma rangeli | 57% | 100% |
A0A3S5H4Z8 | Leishmania donovani | 93% | 100% |
A4HRN4 | Leishmania infantum | 93% | 100% |
A8X379 | Caenorhabditis briggsae | 31% | 100% |
C9ZJ16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9ACB2 | Leishmania major | 91% | 99% |
E9AJK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F1LMZ8 | Rattus norvegicus | 41% | 100% |
F1QGH9 | Danio rerio | 42% | 100% |
F6P3G4 | Danio rerio | 42% | 100% |
F6XBL2 | Xenopus tropicalis | 41% | 100% |
O00231 | Homo sapiens | 41% | 100% |
P34481 | Caenorhabditis elegans | 32% | 100% |
Q12377 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
Q20938 | Caenorhabditis elegans | 38% | 100% |
Q2KI42 | Bos taurus | 41% | 100% |
Q54UB5 | Dictyostelium discoideum | 37% | 100% |
Q7KLV9 | Drosophila melanogaster | 38% | 100% |
Q8BG32 | Mus musculus | 41% | 100% |
Q9LP45 | Arabidopsis thaliana | 46% | 100% |
Q9P7S2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |