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: 1, no: 29 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005819 | spindle | 5 | 3 |
GO:0005930 | axoneme | 2 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0072686 | mitotic spindle | 6 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9AI34
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 3 |
GO:0000281 | mitotic cytokinesis | 4 | 3 |
GO:0000910 | cytokinesis | 3 | 3 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 3 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0007010 | cytoskeleton organization | 5 | 3 |
GO:0007017 | microtubule-based process | 2 | 3 |
GO:0007051 | spindle organization | 3 | 3 |
GO:0007052 | mitotic spindle organization | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0022402 | cell cycle process | 2 | 3 |
GO:0048870 | cell motility | 2 | 3 |
GO:0060285 | cilium-dependent cell motility | 4 | 3 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 3 |
GO:1903047 | mitotic cell cycle process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 20 |
GO:0005509 | calcium ion binding | 5 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043169 | cation binding | 3 | 19 |
GO:0046872 | metal ion binding | 4 | 19 |
GO:0005515 | protein binding | 2 | 3 |
GO:0008092 | cytoskeletal protein binding | 3 | 3 |
GO:0015631 | tubulin binding | 4 | 3 |
GO:0043014 | alpha-tubulin binding | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 738 | 742 | PF00656 | 0.546 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.606 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.426 |
CLV_PCSK_FUR_1 | 58 | 62 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 837 | 839 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 837 | 839 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.392 |
DEG_SPOP_SBC_1 | 855 | 859 | PF00917 | 0.538 |
DOC_ANK_TNKS_1 | 291 | 298 | PF00023 | 0.541 |
DOC_CKS1_1 | 779 | 784 | PF01111 | 0.448 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 32 | PF00134 | 0.586 |
DOC_CYCLIN_yCln2_LP_2 | 408 | 414 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 484 | 490 | PF00134 | 0.542 |
DOC_MAPK_DCC_7 | 541 | 549 | PF00069 | 0.368 |
DOC_MAPK_DCC_7 | 776 | 785 | PF00069 | 0.425 |
DOC_MAPK_FxFP_2 | 808 | 811 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 140 | 146 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 274 | 283 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 301 | 309 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 527 | 534 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 642 | 650 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 277 | 285 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.428 |
DOC_PP1_RVXF_1 | 269 | 276 | PF00149 | 0.484 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.376 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.548 |
DOC_PP4_FxxP_1 | 771 | 774 | PF00568 | 0.668 |
DOC_PP4_FxxP_1 | 808 | 811 | PF00568 | 0.379 |
DOC_SPAK_OSR1_1 | 496 | 500 | PF12202 | 0.528 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 727 | 731 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.616 |
DOC_USP7_UBL2_3 | 529 | 533 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.419 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 319 | 329 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 495 | 500 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 702 | 706 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 752 | 758 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 96 | 103 | PF00244 | 0.618 |
LIG_APCC_ABBA_1 | 305 | 310 | PF00400 | 0.517 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.661 |
LIG_BIR_III_4 | 454 | 458 | PF00653 | 0.552 |
LIG_BIR_III_4 | 607 | 611 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.570 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.580 |
LIG_BRCT_BRCA1_1 | 504 | 508 | PF00533 | 0.576 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.459 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.410 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.484 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.659 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.383 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.717 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.605 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.381 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.467 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.488 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.634 |
LIG_FHA_2 | 684 | 690 | PF00498 | 0.412 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.631 |
LIG_FHA_2 | 796 | 802 | PF00498 | 0.409 |
LIG_GBD_Chelix_1 | 618 | 626 | PF00786 | 0.473 |
LIG_Integrin_RGD_1 | 765 | 767 | PF01839 | 0.433 |
LIG_LIR_Apic_2 | 770 | 774 | PF02991 | 0.607 |
LIG_LIR_Apic_2 | 807 | 811 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 636 | 643 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 682 | 691 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 636 | 640 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 807 | 813 | PF02991 | 0.476 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.681 |
LIG_PCNA_PIPBox_1 | 802 | 811 | PF02747 | 0.400 |
LIG_PCNA_yPIPBox_3 | 80 | 90 | PF02747 | 0.410 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.462 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.493 |
LIG_REV1ctd_RIR_1 | 397 | 407 | PF16727 | 0.364 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 818 | 821 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.363 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.561 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.408 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.747 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.555 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.509 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.553 |
LIG_SH3_3 | 808 | 814 | PF00018 | 0.446 |
LIG_SH3_CIN85_PxpxPR_1 | 536 | 541 | PF14604 | 0.558 |
LIG_SUMO_SIM_anti_2 | 313 | 318 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 686 | 692 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 410 | 415 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 611 | 616 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 645 | 652 | PF11976 | 0.440 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.661 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.506 |
LIG_TRAF2_2 | 72 | 77 | PF00917 | 0.457 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.441 |
LIG_WRC_WIRS_1 | 634 | 639 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 768 | 773 | PF05994 | 0.699 |
LIG_WW_3 | 30 | 34 | PF00397 | 0.609 |
MOD_CDK_SPxK_1 | 674 | 680 | PF00069 | 0.308 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.420 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.720 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.610 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.351 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.337 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.561 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.420 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.457 |
MOD_Cter_Amidation | 58 | 61 | PF01082 | 0.487 |
MOD_Cter_Amidation | 762 | 765 | PF01082 | 0.627 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.324 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.512 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.652 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.758 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.332 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.494 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.685 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.349 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.402 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.634 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.497 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.446 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.369 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.711 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.461 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.641 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.551 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.630 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.259 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.199 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.654 |
MOD_N-GLC_1 | 823 | 828 | PF02516 | 0.552 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.353 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.405 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.451 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.621 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.674 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.386 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.524 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.495 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.315 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.376 |
MOD_NEK2_2 | 474 | 479 | PF00069 | 0.259 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.533 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.635 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.420 |
MOD_PK_1 | 338 | 344 | PF00069 | 0.400 |
MOD_PKA_1 | 495 | 501 | PF00069 | 0.369 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.369 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.344 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.676 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.348 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.568 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.595 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.676 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.644 |
MOD_PKA_2 | 775 | 781 | PF00069 | 0.507 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.682 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.331 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.514 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.317 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.346 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.535 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.700 |
MOD_Plk_2-3 | 695 | 701 | PF00069 | 0.552 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.391 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.205 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.560 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.497 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.739 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.517 |
MOD_Plk_4 | 843 | 849 | PF00069 | 0.636 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.587 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.411 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.420 |
MOD_SUMO_rev_2 | 559 | 567 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 713 | 723 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 730 | 738 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 563 | 568 | PF01217 | 0.175 |
TRG_DiLeu_BaEn_2 | 303 | 309 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_4 | 189 | 195 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 839 | 842 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 785 | 787 | PF00400 | 0.412 |
TRG_NLS_MonoCore_2 | 526 | 531 | PF00514 | 0.441 |
TRG_NLS_MonoExtN_4 | 527 | 532 | PF00514 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 731 | 735 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 787 | 791 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 69% | 100% |
A0A0N1HZ98 | Leptomonas seymouri | 23% | 100% |
A0A0N1I3M2 | Leptomonas seymouri | 21% | 100% |
A0A0S4IJW8 | Bodo saltans | 35% | 100% |
A0A0S4IQM0 | Bodo saltans | 25% | 100% |
A0A0S4J8J7 | Bodo saltans | 24% | 94% |
A0A1X0NEV8 | Trypanosomatidae | 46% | 100% |
A0A1X0P419 | Trypanosomatidae | 23% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 24% | 100% |
A0A3Q8IPU3 | Leishmania donovani | 23% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 48% | 100% |
A0A3R7L048 | Trypanosoma rangeli | 23% | 100% |
A0A3S5H688 | Leishmania donovani | 87% | 99% |
A0A422NK00 | Trypanosoma rangeli | 27% | 100% |
A4HE78 | Leishmania braziliensis | 24% | 100% |
A4HFK9 | Leishmania braziliensis | 23% | 100% |
A4HTP5 | Leishmania infantum | 87% | 99% |
A4I1J2 | Leishmania infantum | 24% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AD64 | Leishmania major | 23% | 100% |
E9AHF6 | Leishmania infantum | 23% | 100% |
E9AMI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
Q4Q9U5 | Leishmania major | 24% | 99% |
Q4QI57 | Leishmania major | 87% | 100% |
V5ASV2 | Trypanosoma cruzi | 24% | 100% |
V5D3X9 | Trypanosoma cruzi | 23% | 100% |