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. | yes | 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. | yes | 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:0005737 | cytoplasm | 2 | 2 |
GO:0008541 | proteasome regulatory particle, lid subcomplex | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0000502 | proteasome complex | 3 | 9 |
GO:0140535 | intracellular protein-containing complex | 2 | 9 |
GO:1902494 | catalytic complex | 2 | 9 |
GO:1905368 | peptidase complex | 3 | 9 |
GO:1905369 | endopeptidase complex | 4 | 9 |
Related structures:
AlphaFold database: E9ACB2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.755 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.306 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.814 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.808 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.703 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.694 |
CLV_PCSK_PC7_1 | 521 | 527 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.306 |
CLV_Separin_Metazoa | 336 | 340 | PF03568 | 0.601 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.624 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.402 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.506 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.519 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.542 |
DOC_CYCLIN_RxL_1 | 25 | 34 | PF00134 | 0.552 |
DOC_CYCLIN_RxL_1 | 349 | 359 | PF00134 | 0.494 |
DOC_CYCLIN_RxL_1 | 89 | 99 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 254 | 262 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 168 | 176 | PF00069 | 0.380 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.797 |
DOC_USP7_UBL2_3 | 462 | 466 | PF12436 | 0.518 |
DOC_USP7_UBL2_3 | 92 | 96 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 147 | 155 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 199 | 206 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 25 | 32 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 342 | 358 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 380 | 396 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 404 | 409 | PF00400 | 0.586 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.644 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.506 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.562 |
LIG_eIF4E_1 | 56 | 62 | PF01652 | 0.562 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.525 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.601 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.594 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.506 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.603 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.591 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.454 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.552 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.539 |
LIG_Integrin_RGD_1 | 22 | 24 | PF01839 | 0.527 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 305 | 312 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.470 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.453 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.464 |
LIG_NRBOX | 57 | 63 | PF00104 | 0.535 |
LIG_PCNA_yPIPBox_3 | 453 | 466 | PF02747 | 0.622 |
LIG_Rb_pABgroove_1 | 454 | 462 | PF01858 | 0.485 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.450 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.483 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.387 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.506 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.506 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.477 |
LIG_SH2_GRB2like | 426 | 429 | PF00017 | 0.745 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.743 |
LIG_SH2_PTP2 | 138 | 141 | PF00017 | 0.517 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.517 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.745 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.743 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.547 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.601 |
LIG_SUMO_SIM_par_1 | 166 | 173 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.536 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.408 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.606 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.521 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.387 |
LIG_UBA3_1 | 307 | 314 | PF00899 | 0.419 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.473 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.549 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.475 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.516 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.484 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.485 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.250 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.383 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.553 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.506 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.479 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.427 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.383 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.544 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.608 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.545 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.547 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.694 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.396 |
MOD_GlcNHglycan | 320 | 324 | PF01048 | 0.404 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.636 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.773 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.468 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.611 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.502 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.484 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.459 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.361 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.657 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.362 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.454 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.466 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.361 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.488 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.359 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.361 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.460 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.553 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.352 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.473 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.468 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.557 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.421 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.458 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.558 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.462 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.440 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.481 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.579 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.361 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.429 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.364 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.535 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.459 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.486 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.473 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.750 |
MOD_SUMO_rev_2 | 173 | 181 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 225 | 232 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 376 | 385 | PF00179 | 0.403 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_2 | 124 | 130 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.389 |
TRG_NES_CRM1_1 | 30 | 46 | PF08389 | 0.405 |
TRG_NES_CRM1_1 | 365 | 376 | PF08389 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3L4 | Leptomonas seymouri | 79% | 100% |
A0A0S4JHD2 | Bodo saltans | 55% | 100% |
A0A1X0NKK6 | Trypanosomatidae | 59% | 93% |
A0A3R7KIY0 | Trypanosoma rangeli | 58% | 100% |
A0A3S5H4Z8 | Leishmania donovani | 97% | 100% |
A4H3D3 | Leishmania braziliensis | 91% | 99% |
A4HRN4 | Leishmania infantum | 97% | 100% |
A8X379 | Caenorhabditis briggsae | 30% | 100% |
C9ZJ16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AJK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
F1LMZ8 | Rattus norvegicus | 42% | 100% |
F1QGH9 | Danio rerio | 43% | 100% |
F6P3G4 | Danio rerio | 43% | 100% |
F6XBL2 | Xenopus tropicalis | 42% | 100% |
O00231 | Homo sapiens | 42% | 100% |
P34481 | Caenorhabditis elegans | 31% | 100% |
Q12377 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q20938 | Caenorhabditis elegans | 38% | 100% |
Q2KI42 | Bos taurus | 42% | 100% |
Q54UB5 | Dictyostelium discoideum | 37% | 100% |
Q7KLV9 | Drosophila melanogaster | 40% | 100% |
Q8BG32 | Mus musculus | 42% | 100% |
Q9LP45 | Arabidopsis thaliana | 46% | 100% |
Q9P7S2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |