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: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AV07
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 10 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009057 | macromolecule catabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016579 | protein deubiquitination | 6 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 10 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0070646 | protein modification by small protein removal | 5 | 10 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 10 |
GO:0008233 | peptidase activity | 3 | 10 |
GO:0008234 | cysteine-type peptidase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 10 |
GO:0101005 | deubiquitinase activity | 5 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.358 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.453 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.297 |
DEG_APCC_DBOX_1 | 560 | 568 | PF00400 | 0.387 |
DEG_APCC_KENBOX_2 | 343 | 347 | PF00400 | 0.309 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.459 |
DEG_SCF_FBW7_1 | 22 | 29 | PF00400 | 0.588 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 526 | 530 | PF00917 | 0.398 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.234 |
DEG_SPOP_SBC_1 | 632 | 636 | PF00917 | 0.309 |
DOC_MAPK_gen_1 | 323 | 330 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 484 | 491 | PF00069 | 0.279 |
DOC_MAPK_HePTP_8 | 402 | 414 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 377 | 386 | PF00069 | 0.161 |
DOC_MAPK_MEF2A_6 | 405 | 414 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.387 |
DOC_MAPK_RevD_3 | 456 | 472 | PF00069 | 0.272 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.594 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.461 |
DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.297 |
DOC_PP4_FxxP_1 | 623 | 626 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.328 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.374 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.617 |
LIG_APCC_ABBAyCdc20_2 | 405 | 411 | PF00400 | 0.387 |
LIG_BIR_III_4 | 628 | 632 | PF00653 | 0.387 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.721 |
LIG_CaM_IQ_9 | 470 | 486 | PF13499 | 0.361 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.516 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.332 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.328 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.445 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.365 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.380 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.161 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.387 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.280 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.729 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.555 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.371 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.334 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.387 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.308 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 118 | 122 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 427 | 432 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 635 | 646 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 635 | 641 | PF02991 | 0.274 |
LIG_PCNA_PIPBox_1 | 494 | 503 | PF02747 | 0.387 |
LIG_PTB_Apo_2 | 191 | 198 | PF02174 | 0.251 |
LIG_PTB_Phospho_1 | 191 | 197 | PF10480 | 0.251 |
LIG_Rb_LxCxE_1 | 438 | 455 | PF01857 | 0.161 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.649 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.272 |
LIG_SH2_NCK_1 | 642 | 646 | PF00017 | 0.343 |
LIG_SH2_PTP2 | 638 | 641 | PF00017 | 0.297 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.272 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 598 | 601 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.173 |
LIG_SH3_2 | 72 | 77 | PF14604 | 0.647 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.668 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.332 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.597 |
LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.617 |
LIG_TRAF2_1 | 556 | 559 | PF00917 | 0.378 |
LIG_TYR_ITIM | 640 | 645 | PF00017 | 0.309 |
LIG_UBA3_1 | 243 | 249 | PF00899 | 0.272 |
LIG_UBA3_1 | 466 | 471 | PF00899 | 0.272 |
LIG_WRC_WIRS_1 | 550 | 555 | PF05994 | 0.161 |
MOD_CDC14_SPxK_1 | 74 | 77 | PF00782 | 0.648 |
MOD_CDK_SPK_2 | 128 | 133 | PF00069 | 0.438 |
MOD_CDK_SPxK_1 | 22 | 28 | PF00069 | 0.587 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.648 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 71 | 78 | PF00069 | 0.651 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.570 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.581 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.666 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.547 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.666 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.387 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.345 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.654 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.579 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.302 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.373 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.365 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.310 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.672 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.634 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.611 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.692 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.296 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.738 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.278 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.319 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.322 |
MOD_GlcNHglycan | 534 | 538 | PF01048 | 0.241 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.324 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.526 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.515 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.550 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.672 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.587 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.587 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.419 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.307 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.290 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.371 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.433 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.301 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.384 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.592 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.560 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.387 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.332 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.305 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.652 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.528 |
MOD_N-GLC_2 | 194 | 196 | PF02516 | 0.251 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.611 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.691 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.474 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.387 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.346 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.398 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.640 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.730 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.272 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.577 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.272 |
MOD_NEK2_2 | 452 | 457 | PF00069 | 0.371 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.487 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.703 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.671 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.326 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.371 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.186 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.609 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.363 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.414 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.289 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.297 |
MOD_Plk_2-3 | 499 | 505 | PF00069 | 0.387 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.626 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.387 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.272 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.272 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.297 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.580 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.584 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.568 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.561 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.587 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.563 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.297 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.641 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.309 |
MOD_SUMO_for_1 | 316 | 319 | PF00179 | 0.309 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.316 |
MOD_SUMO_rev_2 | 444 | 449 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 7 | 17 | PF00179 | 0.589 |
TRG_DiLeu_BaEn_2 | 288 | 294 | PF01217 | 0.272 |
TRG_DiLeu_BaEn_2 | 574 | 580 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.173 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 560 | 562 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 603 | 605 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.460 |
TRG_NLS_MonoExtN_4 | 561 | 566 | PF00514 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 23% | 80% |
A0A0N0P852 | Leptomonas seymouri | 69% | 85% |
A0A0S4IVV7 | Bodo saltans | 23% | 100% |
A0A3Q8IB18 | Leishmania donovani | 92% | 90% |
A0A422MZT5 | Trypanosoma rangeli | 41% | 100% |
A4HBN8 | Leishmania braziliensis | 78% | 100% |
A4HZ39 | Leishmania infantum | 92% | 90% |
D0A1P0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 98% |
P39944 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 80% |
Q4QCH5 | Leishmania major | 90% | 100% |
Q8IQ27 | Drosophila melanogaster | 24% | 69% |
Q91W36 | Mus musculus | 23% | 100% |
V5DGZ8 | Trypanosoma cruzi | 40% | 99% |