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 | yes | yes: 7, no: 2 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9ACY9
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.303 |
CLV_PCSK_FUR_1 | 294 | 298 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.682 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.444 |
DEG_SCF_FBW7_1 | 140 | 145 | PF00400 | 0.423 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.428 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.478 |
DOC_CYCLIN_RxL_1 | 475 | 487 | PF00134 | 0.591 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.389 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.448 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.691 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.383 |
DOC_PP2B_PxIxI_1 | 71 | 77 | PF00149 | 0.288 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 485 | 501 | PF00022 | 0.485 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.643 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 558 | 562 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 575 | 579 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.445 |
LIG_Clathr_ClatBox_1 | 560 | 564 | PF01394 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 513 | 516 | PF00928 | 0.461 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.423 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.516 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.496 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.363 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.503 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.429 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.469 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.475 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.378 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.409 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 277 | 284 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 319 | 327 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 448 | 458 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 559 | 570 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 572 | 582 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 319 | 323 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.325 |
LIG_LYPXL_SIV_4 | 526 | 534 | PF13949 | 0.485 |
LIG_MLH1_MIPbox_1 | 558 | 562 | PF16413 | 0.471 |
LIG_NRBOX | 553 | 559 | PF00104 | 0.382 |
LIG_Pex14_1 | 585 | 589 | PF04695 | 0.361 |
LIG_Pex14_2 | 477 | 481 | PF04695 | 0.558 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.503 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.677 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.380 |
LIG_SH3_2 | 364 | 369 | PF14604 | 0.734 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.417 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.751 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.742 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.606 |
LIG_SUMO_SIM_anti_2 | 237 | 244 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 12 | 18 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 34 | 40 | PF11976 | 0.411 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.742 |
LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.425 |
LIG_TYR_ITSM | 446 | 453 | PF00017 | 0.549 |
LIG_UBA3_1 | 211 | 216 | PF00899 | 0.433 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 317 | 322 | PF05994 | 0.557 |
LIG_WRC_WIRS_1 | 602 | 607 | PF05994 | 0.648 |
LIG_WRC_WIRS_1 | 612 | 617 | PF05994 | 0.658 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.449 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.495 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.418 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.382 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.453 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.681 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.746 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.485 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.644 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.641 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.579 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.631 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.408 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.385 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.402 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.635 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.405 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.460 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.698 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.639 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.374 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.426 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.478 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.369 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.527 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.353 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.423 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.242 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.580 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.488 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.601 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.381 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.485 |
MOD_N-GLC_2 | 349 | 351 | PF02516 | 0.471 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.428 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.540 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.329 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.441 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.727 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.413 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.498 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.347 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.454 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.609 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.361 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.515 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.227 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.689 |
MOD_PIKK_1 | 627 | 633 | PF00454 | 0.679 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.545 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.642 |
MOD_PKB_1 | 125 | 133 | PF00069 | 0.324 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.392 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.717 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.401 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.477 |
MOD_Plk_1 | 585 | 591 | PF00069 | 0.308 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.431 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.439 |
MOD_Plk_2-3 | 613 | 619 | PF00069 | 0.715 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.405 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.420 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.678 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.698 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.574 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.678 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.365 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.420 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.668 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.374 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.296 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.566 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.421 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.394 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.647 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.548 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.565 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.647 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 552 | 564 | PF08389 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAS2 | Leptomonas seymouri | 55% | 100% |
A0A3Q8IHD5 | Leishmania donovani | 93% | 100% |
A0A3R7MRQ1 | Trypanosoma rangeli | 32% | 97% |
A4HFD1 | Leishmania braziliensis | 74% | 100% |
A4I364 | Leishmania infantum | 93% | 100% |
C9ZKV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 87% |
E9AYR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BGA4 | Trypanosoma cruzi | 33% | 93% |