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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4IDY7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 658 | 662 | PF00656 | 0.352 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.413 |
CLV_PCSK_FUR_1 | 392 | 396 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.330 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 627 | 635 | PF00400 | 0.405 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.593 |
DOC_CDC14_PxL_1 | 514 | 522 | PF14671 | 0.560 |
DOC_CYCLIN_RxL_1 | 538 | 547 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 622 | 633 | PF00134 | 0.304 |
DOC_CYCLIN_RxL_1 | 661 | 671 | PF00134 | 0.374 |
DOC_MAPK_DCC_7 | 39 | 47 | PF00069 | 0.497 |
DOC_MAPK_FxFP_2 | 202 | 205 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 23 | 30 | PF00069 | 0.494 |
DOC_MAPK_JIP1_4 | 181 | 187 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 322 | 330 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 662 | 669 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 143 | 153 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 181 | 186 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 439 | 443 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 444 | 453 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 555 | 559 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 64 | 70 | PF00244 | 0.296 |
LIG_Actin_WH2_2 | 542 | 557 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 56 | 73 | PF00022 | 0.454 |
LIG_CtBP_PxDLS_1 | 466 | 470 | PF00389 | 0.539 |
LIG_DLG_GKlike_1 | 159 | 167 | PF00625 | 0.324 |
LIG_EH1_1 | 497 | 505 | PF00400 | 0.396 |
LIG_eIF4E_1 | 498 | 504 | PF01652 | 0.448 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.279 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.357 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.311 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.378 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.420 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.502 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.343 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.620 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.422 |
LIG_LIR_Apic_2 | 403 | 409 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 533 | 542 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 533 | 537 | PF02991 | 0.492 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.375 |
LIG_NRBOX | 609 | 615 | PF00104 | 0.431 |
LIG_Pex14_1 | 635 | 639 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.495 |
LIG_RPA_C_Fungi | 10 | 22 | PF08784 | 0.394 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.424 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 406 | 410 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 413 | 416 | PF00017 | 0.428 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.434 |
LIG_SH2_SRC | 95 | 98 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 639 | 643 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.461 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.423 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 183 | 189 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 478 | 486 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 540 | 547 | PF11976 | 0.469 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.506 |
LIG_TRFH_1 | 406 | 410 | PF08558 | 0.536 |
LIG_TYR_ITIM | 503 | 508 | PF00017 | 0.490 |
LIG_UBA3_1 | 236 | 242 | PF00899 | 0.357 |
LIG_UBA3_1 | 606 | 611 | PF00899 | 0.420 |
LIG_WRC_WIRS_1 | 160 | 165 | PF05994 | 0.360 |
MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 387 | 394 | PF00069 | 0.514 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.683 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.374 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.644 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.802 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.628 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.324 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.408 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.292 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.379 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.418 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.455 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.507 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.618 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.357 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.528 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.600 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.348 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.634 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.442 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.342 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.444 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.736 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.419 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.510 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.481 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.329 |
MOD_LATS_1 | 303 | 309 | PF00433 | 0.361 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.426 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.447 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.627 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.416 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.744 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.356 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.367 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.439 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.394 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.360 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.439 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.473 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.558 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.576 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.338 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.315 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.339 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.420 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.329 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.556 |
MOD_PK_1 | 479 | 485 | PF00069 | 0.388 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.541 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.328 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.642 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.431 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.599 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.444 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.437 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.476 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.378 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.575 |
MOD_PKB_1 | 179 | 187 | PF00069 | 0.410 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.365 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.537 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.422 |
MOD_Plk_2-3 | 595 | 601 | PF00069 | 0.399 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.356 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.465 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.350 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.363 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.320 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.310 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.613 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.629 |
TRG_DiLeu_BaEn_1 | 109 | 114 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 33 | 38 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_1 | 449 | 454 | PF01217 | 0.406 |
TRG_DiLeu_BaEn_1 | 642 | 647 | PF01217 | 0.374 |
TRG_DiLeu_BaEn_4 | 582 | 588 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 661 | 666 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.520 |
TRG_NES_CRM1_1 | 319 | 333 | PF08389 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMS6 | Leptomonas seymouri | 65% | 99% |
A0A0S4IXA8 | Bodo saltans | 28% | 95% |
A0A1X0NNB6 | Trypanosomatidae | 42% | 100% |
A0A3Q8IHX9 | Leishmania donovani | 100% | 100% |
A4HQ89 | Leishmania braziliensis | 80% | 100% |
D0A422 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AU07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0I8 | Leishmania major | 94% | 100% |
V5B3L6 | Trypanosoma cruzi | 43% | 100% |