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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: E9ALI2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.782 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.650 |
CLV_PCSK_FUR_1 | 179 | 183 | PF00082 | 0.576 |
CLV_PCSK_FUR_1 | 268 | 272 | PF00082 | 0.449 |
CLV_PCSK_FUR_1 | 449 | 453 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.741 |
CLV_PCSK_PC7_1 | 447 | 453 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.649 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.500 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.457 |
DEG_COP1_1 | 199 | 207 | PF00400 | 0.521 |
DEG_COP1_1 | 222 | 232 | PF00400 | 0.423 |
DEG_SPOP_SBC_1 | 541 | 545 | PF00917 | 0.561 |
DEG_SPOP_SBC_1 | 614 | 618 | PF00917 | 0.779 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.616 |
DOC_CYCLIN_yCln2_LP_2 | 307 | 313 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 139 | 149 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 84 | 94 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.649 |
DOC_PP1_RVXF_1 | 291 | 298 | PF00149 | 0.524 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.459 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.696 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.632 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 575 | 582 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 91 | 101 | PF00244 | 0.495 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.699 |
LIG_deltaCOP1_diTrp_1 | 294 | 304 | PF00928 | 0.595 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 166 | 171 | PF02991 | 0.744 |
LIG_LIR_Apic_2 | 382 | 387 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.662 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.532 |
LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.659 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.477 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.582 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.394 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.583 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.661 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.670 |
LIG_SUMO_SIM_anti_2 | 145 | 151 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 585 | 591 | PF11976 | 0.407 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.589 |
MOD_CDC14_SPxK_1 | 41 | 44 | PF00782 | 0.576 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.768 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.636 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.639 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.674 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.542 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.494 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.745 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.524 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.641 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.739 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.751 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.758 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.528 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.472 |
MOD_Cter_Amidation | 620 | 623 | PF01082 | 0.674 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.667 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.518 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.793 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.596 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.682 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.531 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.639 |
MOD_GlcNHglycan | 392 | 396 | PF01048 | 0.703 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.630 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.522 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.677 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.710 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.624 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.713 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.687 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.706 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.575 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.587 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.624 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.724 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.703 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.515 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.602 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.682 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.641 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.487 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.584 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.617 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.732 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.555 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.669 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.789 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.497 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.676 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.708 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.364 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.555 |
MOD_PK_1 | 623 | 629 | PF00069 | 0.472 |
MOD_PK_1 | 638 | 644 | PF00069 | 0.466 |
MOD_PKA_1 | 622 | 628 | PF00069 | 0.515 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.523 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.390 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.645 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.583 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.666 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.629 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.567 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.532 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.466 |
MOD_Plk_2-3 | 386 | 392 | PF00069 | 0.543 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.675 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.653 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.519 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.748 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.653 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.580 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.494 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.766 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.653 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.528 |
MOD_SUMO_rev_2 | 127 | 135 | PF00179 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 117 | 122 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 178 | 181 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 447 | 449 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 181 | 185 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 289 | 294 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Y8 | Leptomonas seymouri | 62% | 97% |
A0A0S4IQ31 | Bodo saltans | 31% | 100% |
A0A0S4JIT3 | Bodo saltans | 27% | 100% |
A0A0S4JQK5 | Bodo saltans | 26% | 100% |
A0A0S4JTQ5 | Bodo saltans | 25% | 87% |
A0A1X0P950 | Trypanosomatidae | 34% | 96% |
A0A3Q8IRK3 | Leishmania donovani | 87% | 96% |
A0A3R7MS13 | Trypanosoma rangeli | 34% | 99% |
A0A3S5H6B0 | Leishmania donovani | 26% | 100% |
A0A422N6D6 | Trypanosoma rangeli | 25% | 100% |
A4HHP1 | Leishmania braziliensis | 74% | 100% |
A4HTT0 | Leishmania infantum | 25% | 100% |
A4I4V6 | Leishmania infantum | 87% | 78% |
E9AEA4 | Leishmania major | 82% | 97% |
E9AML3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4QI23 | Leishmania major | 25% | 100% |
V5BC37 | Trypanosoma cruzi | 36% | 99% |