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: A4H405
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009306 | protein secretion | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0030254 | protein secretion by the type III secretion system | 4 | 10 |
GO:0032940 | secretion by cell | 3 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0035592 | establishment of protein localization to extracellular region | 4 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046903 | secretion | 4 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0055085 | transmembrane transport | 2 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071692 | protein localization to extracellular region | 5 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071806 | protein transmembrane transport | 3 | 10 |
GO:0140352 | export from cell | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.400 |
CLV_PCSK_FUR_1 | 278 | 282 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 276 | 282 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.554 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.498 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.376 |
DOC_CYCLIN_RxL_1 | 138 | 148 | PF00134 | 0.610 |
DOC_CYCLIN_RxL_1 | 290 | 301 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 760 | 770 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 763 | 772 | PF00069 | 0.330 |
DOC_PP2B_LxvP_1 | 552 | 555 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 672 | 675 | PF13499 | 0.620 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 667 | 672 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 168 | 172 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 226 | 234 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 39 | 43 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 416 | 421 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 577 | 587 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 636 | 645 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 650 | 656 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 448 | 464 | PF00022 | 0.275 |
LIG_APCC_ABBA_1 | 770 | 775 | PF00400 | 0.203 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_CtBP_PxDLS_1 | 456 | 462 | PF00389 | 0.389 |
LIG_eIF4E_1 | 495 | 501 | PF01652 | 0.490 |
LIG_eIF4E_1 | 705 | 711 | PF01652 | 0.308 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.344 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.483 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.449 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.489 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.459 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.563 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.404 |
LIG_FHA_1 | 769 | 775 | PF00498 | 0.355 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.436 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.636 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.444 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.444 |
LIG_IRF3_LxIS_1 | 129 | 134 | PF10401 | 0.498 |
LIG_LIR_Gen_1 | 214 | 224 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 544 | 553 | PF02991 | 0.474 |
LIG_LIR_LC3C_4 | 707 | 712 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 742 | 746 | PF02991 | 0.400 |
LIG_Rb_pABgroove_1 | 481 | 489 | PF01858 | 0.502 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.488 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.447 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.447 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.447 |
LIG_SH2_CRK | 676 | 680 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 487 | 491 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 676 | 680 | PF00017 | 0.480 |
LIG_SH2_SRC | 495 | 498 | PF00017 | 0.490 |
LIG_SH2_SRC | 705 | 708 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.556 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.440 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.660 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.583 |
LIG_SH3_3 | 631 | 637 | PF00018 | 0.542 |
LIG_SUMO_SIM_anti_2 | 482 | 489 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 706 | 713 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 128 | 135 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.637 |
LIG_SUMO_SIM_par_1 | 468 | 478 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 87 | 92 | PF11976 | 0.412 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.561 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.495 |
LIG_TYR_ITAM | 478 | 500 | PF00017 | 0.447 |
LIG_TYR_ITIM | 485 | 490 | PF00017 | 0.389 |
LIG_UBA3_1 | 253 | 261 | PF00899 | 0.524 |
MOD_CDC14_SPxK_1 | 633 | 636 | PF00782 | 0.480 |
MOD_CDK_SPK_2 | 643 | 648 | PF00069 | 0.479 |
MOD_CDK_SPxK_1 | 630 | 636 | PF00069 | 0.488 |
MOD_CDK_SPxK_1 | 93 | 99 | PF00069 | 0.559 |
MOD_CDK_SPxxK_3 | 643 | 650 | PF00069 | 0.638 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.627 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.434 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.676 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.631 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.695 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.456 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.631 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.593 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.512 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.444 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.451 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.466 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.628 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.628 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.611 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.668 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.322 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.498 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.642 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.650 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.744 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.488 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.677 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.571 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.451 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.590 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.469 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.687 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.714 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.742 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.680 |
MOD_N-GLC_1 | 680 | 685 | PF02516 | 0.655 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.534 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.537 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.504 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.682 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.584 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.470 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.463 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.539 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.474 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.615 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.413 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.308 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.543 |
MOD_NEK2_2 | 437 | 442 | PF00069 | 0.434 |
MOD_OFUCOSY | 48 | 55 | PF10250 | 0.457 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.398 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.530 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.485 |
MOD_PIKK_1 | 656 | 662 | PF00454 | 0.667 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.587 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.636 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.524 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.468 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.403 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.629 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.688 |
MOD_PKB_1 | 414 | 422 | PF00069 | 0.631 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.476 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.530 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.469 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.447 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.447 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.506 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.467 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.451 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.404 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.754 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.617 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.506 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.654 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.700 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.754 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.485 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.726 |
MOD_ProDKin_1 | 667 | 673 | PF00069 | 0.581 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.623 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.569 |
MOD_SUMO_for_1 | 254 | 257 | PF00179 | 0.524 |
MOD_SUMO_for_1 | 279 | 282 | PF00179 | 0.348 |
MOD_SUMO_rev_2 | 257 | 263 | PF00179 | 0.454 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_1 | 706 | 711 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.672 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.637 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 647 | 650 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 743 | 745 | PF00400 | 0.414 |
TRG_NES_CRM1_1 | 450 | 463 | PF08389 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 186 | 191 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 316 | 321 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 322 | 327 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 563 | 568 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 745 | 749 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I193 | Leptomonas seymouri | 57% | 99% |
A0A0S4ILT7 | Bodo saltans | 37% | 100% |
A0A1X0NMQ4 | Trypanosomatidae | 35% | 100% |
A0A3R7NDD0 | Trypanosoma rangeli | 35% | 100% |
A0A3S5H5C1 | Leishmania donovani | 78% | 98% |
A4HS67 | Leishmania infantum | 78% | 98% |
E9AK54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 98% |
Q9U110 | Leishmania major | 77% | 100% |