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: A0A3S5H5C1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009306 | protein secretion | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0030254 | protein secretion by the type III secretion system | 4 | 11 |
GO:0032940 | secretion by cell | 3 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0035592 | establishment of protein localization to extracellular region | 4 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046903 | secretion | 4 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0055085 | transmembrane transport | 2 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071692 | protein localization to extracellular region | 5 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071806 | protein transmembrane transport | 3 | 11 |
GO:0140352 | export from cell | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.404 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 696 | 698 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.418 |
CLV_Separin_Metazoa | 165 | 169 | PF03568 | 0.469 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.467 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.431 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.575 |
DEG_SPOP_SBC_1 | 686 | 690 | PF00917 | 0.555 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.421 |
DOC_CKS1_1 | 614 | 619 | PF01111 | 0.597 |
DOC_CKS1_1 | 764 | 769 | PF01111 | 0.237 |
DOC_CYCLIN_RxL_1 | 149 | 159 | PF00134 | 0.611 |
DOC_CYCLIN_RxL_1 | 301 | 312 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 142 | 148 | PF00134 | 0.555 |
DOC_MAPK_DCC_7 | 696 | 704 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 150 | 157 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 464 | 472 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 696 | 704 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 774 | 784 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 696 | 704 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 777 | 786 | PF00069 | 0.335 |
DOC_PP2B_LxvP_1 | 563 | 566 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 683 | 686 | PF13499 | 0.577 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.568 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.292 |
LIG_14-3-3_CanoR_1 | 179 | 183 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 237 | 245 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 588 | 598 | PF00244 | 0.561 |
LIG_Actin_WH2_2 | 459 | 475 | PF00022 | 0.259 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.569 |
LIG_eIF4E_1 | 506 | 512 | PF01652 | 0.467 |
LIG_eIF4E_1 | 719 | 725 | PF01652 | 0.314 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.436 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.436 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.436 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.569 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.631 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.527 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.400 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.360 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.409 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.664 |
LIG_LIR_Gen_1 | 489 | 500 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 555 | 564 | PF02991 | 0.449 |
LIG_LIR_LC3C_4 | 721 | 726 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 756 | 760 | PF02991 | 0.404 |
LIG_Rb_pABgroove_1 | 492 | 500 | PF01858 | 0.482 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.493 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.436 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 498 | 502 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 630 | 634 | PF00017 | 0.561 |
LIG_SH2_SRC | 506 | 509 | PF00017 | 0.467 |
LIG_SH2_SRC | 719 | 722 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 530 | 534 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 630 | 634 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 687 | 691 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 343 | 346 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.532 |
LIG_SH3_2 | 93 | 98 | PF14604 | 0.566 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.415 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.649 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.568 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.602 |
LIG_SUMO_SIM_anti_2 | 225 | 231 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 493 | 499 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 721 | 727 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 153 | 159 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 483 | 489 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 87 | 92 | PF11976 | 0.407 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.563 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.429 |
LIG_TYR_ITAM | 489 | 511 | PF00017 | 0.436 |
LIG_UBA3_1 | 264 | 272 | PF00899 | 0.519 |
LIG_WW_3 | 95 | 99 | PF00397 | 0.700 |
MOD_CDK_SPK_2 | 113 | 118 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.615 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.429 |
MOD_CDK_SPxxK_3 | 654 | 661 | PF00069 | 0.638 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.670 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.606 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.674 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.600 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.621 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.446 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.661 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.722 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.587 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.657 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.511 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.447 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.715 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.617 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.674 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.646 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.317 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.757 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.772 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.763 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.519 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.492 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.518 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.736 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.672 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.532 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.622 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.542 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.436 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.507 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.440 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.654 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.709 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.472 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.687 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.649 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.270 |
MOD_N-GLC_2 | 482 | 484 | PF02516 | 0.233 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.541 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.469 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.782 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.647 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.524 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.443 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.522 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.439 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.602 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.527 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.711 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.468 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.270 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.513 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.314 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.426 |
MOD_OFUCOSY | 48 | 55 | PF10250 | 0.464 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.527 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.531 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.555 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.527 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.616 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.493 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.450 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.386 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.612 |
MOD_PKB_1 | 425 | 433 | PF00069 | 0.616 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.476 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.531 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.447 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.399 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.507 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.436 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.437 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.404 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.634 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.726 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.505 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.474 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.542 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.694 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.682 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.712 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.459 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.684 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.494 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.292 |
MOD_SUMO_for_1 | 265 | 268 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 268 | 274 | PF00179 | 0.451 |
TRG_DiLeu_BaEn_1 | 358 | 363 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_1 | 491 | 496 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.640 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 757 | 759 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 461 | 474 | PF08389 | 0.289 |
TRG_NES_CRM1_1 | 60 | 74 | PF08389 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 197 | 202 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 327 | 332 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 464 | 468 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 574 | 579 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 759 | 763 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I193 | Leptomonas seymouri | 58% | 100% |
A0A0S4ILT7 | Bodo saltans | 35% | 100% |
A0A1X0NMQ4 | Trypanosomatidae | 36% | 100% |
A0A3R7NDD0 | Trypanosoma rangeli | 36% | 100% |
A4H405 | Leishmania braziliensis | 78% | 98% |
A4HS67 | Leishmania infantum | 100% | 100% |
E9AK54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q9U110 | Leishmania major | 93% | 100% |
V5BIA8 | Trypanosoma cruzi | 35% | 100% |