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:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AYR4
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
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:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.261 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.707 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.393 |
DEG_COP1_1 | 297 | 306 | PF00400 | 0.498 |
DEG_SCF_FBW7_1 | 140 | 145 | PF00400 | 0.349 |
DEG_SCF_FBW7_2 | 464 | 471 | PF00400 | 0.532 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.392 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.462 |
DOC_CYCLIN_RxL_1 | 475 | 487 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 294 | 303 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 544 | 553 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 31 | 38 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 547 | 555 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.606 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.348 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.374 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.510 |
LIG_Actin_WH2_2 | 485 | 501 | PF00022 | 0.341 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.373 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.603 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 558 | 562 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 575 | 579 | PF00533 | 0.285 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.429 |
LIG_Clathr_ClatBox_1 | 560 | 564 | PF01394 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 513 | 516 | PF00928 | 0.431 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.386 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.251 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.314 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.335 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.453 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.649 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.411 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.287 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.441 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.344 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.553 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.405 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.365 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 278 | 288 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 448 | 458 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 559 | 570 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 572 | 582 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.309 |
LIG_LYPXL_SIV_4 | 526 | 534 | PF13949 | 0.341 |
LIG_NRBOX | 553 | 559 | PF00104 | 0.314 |
LIG_Pex14_1 | 585 | 589 | PF04695 | 0.325 |
LIG_Pex14_2 | 477 | 481 | PF04695 | 0.530 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.460 |
LIG_REV1ctd_RIR_1 | 317 | 326 | PF16727 | 0.485 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 496 | 500 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.312 |
LIG_SH3_2 | 364 | 369 | PF14604 | 0.645 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.377 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.718 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.665 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 237 | 244 | PF11976 | 0.289 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 12 | 18 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 241 | 247 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 34 | 40 | PF11976 | 0.396 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.714 |
LIG_TRFH_1 | 17 | 21 | PF08558 | 0.544 |
LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.324 |
LIG_TYR_ITSM | 446 | 453 | PF00017 | 0.503 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.306 |
LIG_WRC_WIRS_1 | 602 | 607 | PF05994 | 0.631 |
LIG_WRC_WIRS_1 | 612 | 617 | PF05994 | 0.606 |
MOD_CDC14_SPxK_1 | 28 | 31 | PF00782 | 0.380 |
MOD_CDK_SPxK_1 | 25 | 31 | PF00069 | 0.480 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.374 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.387 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.374 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.601 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.386 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.336 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.397 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.648 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.712 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.383 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.341 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.592 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.606 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.602 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.584 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.504 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.281 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.577 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.297 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.370 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.549 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.402 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.353 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.372 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.649 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.418 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.637 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.605 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.326 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.378 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.445 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.309 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.332 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.229 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.537 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.443 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.556 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.383 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.341 |
MOD_N-GLC_2 | 349 | 351 | PF02516 | 0.382 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.389 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.285 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.296 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.308 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.389 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.720 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.375 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.489 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.301 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.409 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.478 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.361 |
MOD_NEK2_2 | 494 | 499 | PF00069 | 0.177 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.407 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.225 |
MOD_PK_1 | 6 | 12 | PF00069 | 0.337 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.510 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.523 |
MOD_PKB_1 | 125 | 133 | PF00069 | 0.278 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.316 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.698 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.355 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.449 |
MOD_Plk_1 | 585 | 591 | PF00069 | 0.259 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.388 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.339 |
MOD_Plk_2-3 | 613 | 619 | PF00069 | 0.621 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.371 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.360 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.585 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.555 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.681 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.296 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.360 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.306 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.253 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.477 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.450 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.351 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.534 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.499 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 151 | 155 | PF00179 | 0.278 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.276 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.443 |
TRG_NES_CRM1_1 | 552 | 564 | PF08389 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAS2 | Leptomonas seymouri | 57% | 99% |
A0A3Q8IHD5 | Leishmania donovani | 92% | 99% |
A0A3R7MRQ1 | Trypanosoma rangeli | 33% | 96% |
A4HFD1 | Leishmania braziliensis | 75% | 99% |
A4I364 | Leishmania infantum | 92% | 99% |
C9ZKV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 86% |
E9ACY9 | Leishmania major | 92% | 100% |
V5BGA4 | Trypanosoma cruzi | 33% | 92% |