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 |
Related structures:
AlphaFold database: E9ANT3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.456 |
CLV_PCSK_FUR_1 | 340 | 344 | PF00082 | 0.650 |
CLV_PCSK_FUR_1 | 444 | 448 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.679 |
CLV_PCSK_PC7_1 | 206 | 212 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.556 |
DEG_APCC_DBOX_1 | 182 | 190 | PF00400 | 0.469 |
DOC_CYCLIN_RxL_1 | 180 | 188 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 247 | 257 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 123 | 130 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 395 | 402 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 444 | 454 | PF00069 | 0.440 |
DOC_MAPK_JIP1_4 | 39 | 45 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.407 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.441 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.720 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.452 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.339 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.478 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.507 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.400 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.755 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.617 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.700 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 3 | 13 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 376 | 382 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 46 | 57 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.476 |
LIG_NRP_CendR_1 | 618 | 620 | PF00754 | 0.641 |
LIG_Pex14_2 | 11 | 15 | PF04695 | 0.443 |
LIG_RPA_C_Fungi | 337 | 349 | PF08784 | 0.597 |
LIG_SH2_CRK | 598 | 602 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 113 | 117 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.479 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.407 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.410 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.521 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.571 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.480 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.527 |
LIG_TRAF2_1 | 540 | 543 | PF00917 | 0.319 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.622 |
LIG_WRC_WIRS_1 | 433 | 438 | PF05994 | 0.433 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.408 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.619 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.484 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.699 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.624 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.454 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.588 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.448 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.471 |
MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.704 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.622 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.483 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.549 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.459 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.685 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.438 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.427 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.424 |
MOD_NEK2_2 | 373 | 378 | PF00069 | 0.634 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.459 |
MOD_OFUCOSY | 92 | 99 | PF10250 | 0.626 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.369 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.668 |
MOD_PK_1 | 138 | 144 | PF00069 | 0.430 |
MOD_PKA_1 | 549 | 555 | PF00069 | 0.476 |
MOD_PKA_1 | 571 | 577 | PF00069 | 0.680 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.463 |
MOD_PKB_1 | 473 | 481 | PF00069 | 0.575 |
MOD_PKB_1 | 547 | 555 | PF00069 | 0.419 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.541 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.627 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.577 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.407 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.521 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.571 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.557 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 199 | 202 | PF00179 | 0.390 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 543 | 552 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.530 |
TRG_DiLeu_LyEn_5 | 180 | 185 | PF01217 | 0.349 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.561 |
TRG_NLS_Bipartite_1 | 560 | 574 | PF00514 | 0.455 |
TRG_NLS_MonoExtN_4 | 104 | 109 | PF00514 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 182 | 187 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 328 | 333 | PF00026 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 531 | 535 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 561 | 566 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK43 | Leptomonas seymouri | 47% | 100% |
A0A1X0NM25 | Trypanosomatidae | 29% | 100% |
A0A3Q8I971 | Leishmania donovani | 86% | 100% |
A0A422N6D2 | Trypanosoma rangeli | 29% | 100% |
A4H6S2 | Leishmania braziliensis | 71% | 100% |
A4HV51 | Leishmania infantum | 86% | 100% |
C9ZQD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
Q4QGT6 | Leishmania major | 83% | 100% |