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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B5K0
Term | Name | Level | Count |
---|---|---|---|
GO:0044145 | modulation of formation of structure involved in a symbiotic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.797 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.810 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 633 | 639 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.771 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.701 |
CLV_Separin_Metazoa | 197 | 201 | PF03568 | 0.374 |
DEG_APCC_DBOX_1 | 430 | 438 | PF00400 | 0.715 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.493 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.686 |
DEG_SCF_FBW7_1 | 135 | 142 | PF00400 | 0.465 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.746 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.464 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.609 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 350 | 358 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 430 | 436 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 549 | 557 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 607 | 613 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 284 | 291 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 284 | 292 | PF00069 | 0.448 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 533 | 536 | PF13499 | 0.650 |
DOC_PP4_FxxP_1 | 591 | 594 | PF00568 | 0.713 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.696 |
DOC_USP7_MATH_2 | 166 | 172 | PF00917 | 0.696 |
DOC_USP7_UBL2_3 | 658 | 662 | PF12436 | 0.776 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 598 | 604 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 655 | 665 | PF00244 | 0.618 |
LIG_Actin_WH2_2 | 137 | 152 | PF00022 | 0.471 |
LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.457 |
LIG_Actin_WH2_2 | 472 | 489 | PF00022 | 0.509 |
LIG_BRCT_BRCA1_1 | 445 | 449 | PF00533 | 0.635 |
LIG_BRCT_BRCA1_1 | 587 | 591 | PF00533 | 0.725 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.699 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.529 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.437 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.574 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.573 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.553 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.474 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.704 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.386 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.633 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 341 | 349 | PF00786 | 0.520 |
LIG_Integrin_RGD_1 | 633 | 635 | PF01839 | 0.593 |
LIG_LIR_Apic_2 | 588 | 594 | PF02991 | 0.687 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 117 | 123 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 643 | 648 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.536 |
LIG_NRBOX | 189 | 195 | PF00104 | 0.462 |
LIG_NRBOX | 71 | 77 | PF00104 | 0.596 |
LIG_PDZ_Class_2 | 669 | 674 | PF00595 | 0.712 |
LIG_Rb_LxCxE_1 | 238 | 259 | PF01857 | 0.613 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.548 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.679 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.452 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.463 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.632 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.757 |
LIG_SUMO_SIM_anti_2 | 180 | 189 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 228 | 235 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 57 | 63 | PF11976 | 0.495 |
LIG_SUMO_SIM_anti_2 | 89 | 94 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 376 | 381 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 529 | 539 | PF11976 | 0.633 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.571 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.612 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.757 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.661 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.559 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.738 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.666 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.460 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.540 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.695 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.543 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.563 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.593 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.620 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.592 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.507 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.661 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.508 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.540 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.658 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.634 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.539 |
MOD_Cter_Amidation | 428 | 431 | PF01082 | 0.724 |
MOD_Cter_Amidation | 635 | 638 | PF01082 | 0.725 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.521 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.716 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.717 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.717 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.540 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.424 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.410 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.390 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.537 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.697 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.582 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.522 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.667 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.494 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.684 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.454 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.638 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.680 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.711 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.525 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.489 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.657 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.623 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.743 |
MOD_LATS_1 | 578 | 584 | PF00433 | 0.588 |
MOD_LATS_1 | 95 | 101 | PF00433 | 0.437 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.655 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.690 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.605 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.763 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.419 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.348 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.414 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.582 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.589 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.666 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.473 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.619 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.659 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.561 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.614 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.433 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.665 |
MOD_PK_1 | 156 | 162 | PF00069 | 0.698 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.603 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.659 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.573 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.496 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.753 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.642 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.505 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.615 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.661 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.628 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.605 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.543 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.449 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.590 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.576 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.760 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.552 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.630 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.631 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.612 |
MOD_SUMO_for_1 | 651 | 654 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 553 | 562 | PF00179 | 0.595 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.569 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.656 |
TRG_DiLeu_BaEn_2 | 608 | 614 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 480 | 485 | PF01217 | 0.582 |
TRG_DiLeu_LyEn_5 | 71 | 76 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.706 |
TRG_NES_CRM1_1 | 181 | 195 | PF08389 | 0.460 |
TRG_NLS_MonoExtC_3 | 35 | 41 | PF00514 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 30 | 35 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 473 | 477 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E6 | Leptomonas seymouri | 47% | 100% |
A0A0S4KLZ0 | Bodo saltans | 27% | 84% |
A0A1X0PAG6 | Trypanosomatidae | 34% | 100% |
A0A3Q8IIY0 | Leishmania donovani | 87% | 100% |
A0A422NVB5 | Trypanosoma rangeli | 32% | 100% |
A4HBC8 | Leishmania braziliensis | 72% | 100% |
A4IAH6 | Leishmania infantum | 87% | 100% |
C9ZLR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4Q2D6 | Leishmania major | 84% | 98% |
V5BRF7 | Trypanosoma cruzi | 33% | 100% |