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: E9APL9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.610 |
CLV_MEL_PAP_1 | 582 | 588 | PF00089 | 0.492 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 704 | 708 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 660 | 662 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.431 |
CLV_Separin_Metazoa | 267 | 271 | PF03568 | 0.453 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.651 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.729 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.402 |
DOC_CYCLIN_RxL_1 | 21 | 32 | PF00134 | 0.561 |
DOC_MAPK_gen_1 | 454 | 463 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.600 |
DOC_PP2B_LxvP_1 | 201 | 204 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.504 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 270 | 275 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 413 | 423 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 457 | 462 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 546 | 556 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 190 | 208 | PF00022 | 0.488 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.725 |
LIG_EVH1_1 | 64 | 68 | PF00568 | 0.510 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.547 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.539 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.576 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.419 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.424 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.524 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.188 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.576 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.586 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.494 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.501 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.546 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.565 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 150 | 156 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 659 | 665 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 666 | 673 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 666 | 671 | PF02991 | 0.585 |
LIG_NRBOX | 566 | 572 | PF00104 | 0.552 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.396 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.527 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.535 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.509 |
LIG_SH2_CRK | 662 | 666 | PF00017 | 0.501 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.536 |
LIG_SH2_GRB2like | 50 | 53 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 70 | 73 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.560 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.366 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.462 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.512 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.438 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.503 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.614 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 44 | 49 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 514 | 520 | PF11976 | 0.526 |
LIG_SxIP_EBH_1 | 153 | 165 | PF03271 | 0.565 |
LIG_SxIP_EBH_1 | 412 | 425 | PF03271 | 0.480 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.614 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.425 |
LIG_TYR_ITIM | 566 | 571 | PF00017 | 0.513 |
LIG_TYR_ITSM | 247 | 254 | PF00017 | 0.528 |
LIG_UBA3_1 | 378 | 383 | PF00899 | 0.434 |
LIG_WW_1 | 67 | 70 | PF00397 | 0.498 |
MOD_CDC14_SPxK_1 | 543 | 546 | PF00782 | 0.642 |
MOD_CDK_SPxK_1 | 540 | 546 | PF00069 | 0.676 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.767 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.389 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.402 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.678 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.484 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.615 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.477 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.623 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.491 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.627 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.539 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.697 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.506 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.520 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.671 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.787 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.469 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.405 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.506 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.496 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.589 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.647 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.349 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.423 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.372 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.405 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.628 |
MOD_GlcNHglycan | 618 | 623 | PF01048 | 0.720 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.706 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.577 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.520 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.525 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.595 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.666 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.458 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.480 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.596 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.518 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.591 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.637 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.571 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.695 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.323 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.443 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.474 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.567 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.474 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.487 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.649 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.486 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.457 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.503 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.610 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.488 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.283 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.396 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.313 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.438 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.503 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.459 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.249 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.453 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.335 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.523 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.563 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.560 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.474 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.680 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.647 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 382 | 385 | PF00179 | 0.480 |
MOD_SUMO_for_1 | 589 | 592 | PF00179 | 0.300 |
MOD_SUMO_rev_2 | 676 | 684 | PF00179 | 0.733 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.624 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B7 | Leptomonas seymouri | 44% | 97% |
A0A1X0NPD4 | Trypanosomatidae | 29% | 86% |
A0A3S5H6R0 | Leishmania donovani | 91% | 100% |
A0A422NXB2 | Trypanosoma rangeli | 30% | 87% |
A4H7I6 | Leishmania braziliensis | 77% | 100% |
A4HVW8 | Leishmania infantum | 92% | 100% |
C9ZT55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 86% |
Q4QFV9 | Leishmania major | 91% | 100% |
V5AXR7 | Trypanosoma cruzi | 29% | 86% |