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: 25 |
NetGPI | no | yes: 0, no: 26 |
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: A0A3S5H688
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 | 18 |
GO:0005509 | calcium ion binding | 5 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043169 | cation binding | 3 | 17 |
GO:0046872 | metal ion binding | 4 | 17 |
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 | 0.532 |
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.761 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.490 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.538 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.576 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 767 | 769 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 864 | 866 | PF00675 | 0.711 |
CLV_PCSK_FUR_1 | 765 | 769 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 767 | 769 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 840 | 842 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 864 | 866 | PF00082 | 0.759 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 840 | 842 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.400 |
DEG_SPOP_SBC_1 | 858 | 862 | PF00917 | 0.529 |
DOC_CKS1_1 | 782 | 787 | PF01111 | 0.435 |
DOC_CYCLIN_RxL_1 | 431 | 439 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 32 | PF00134 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 408 | 414 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 486 | 492 | PF00134 | 0.554 |
DOC_MAPK_DCC_7 | 779 | 788 | PF00069 | 0.419 |
DOC_MAPK_FxFP_2 | 811 | 814 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 140 | 146 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 301 | 309 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 529 | 536 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 644 | 652 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.429 |
DOC_PP1_RVXF_1 | 279 | 286 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.556 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.720 |
DOC_PP4_FxxP_1 | 774 | 777 | PF00568 | 0.642 |
DOC_PP4_FxxP_1 | 811 | 814 | PF00568 | 0.374 |
DOC_SPAK_OSR1_1 | 498 | 502 | PF12202 | 0.502 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 857 | 861 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 535 | 539 | PF12436 | 0.507 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 497 | 502 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 710 | 715 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 755 | 761 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.706 |
LIG_APCC_ABBA_1 | 305 | 310 | PF00400 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BIR_III_4 | 456 | 460 | PF00653 | 0.563 |
LIG_BIR_III_4 | 609 | 613 | PF00653 | 0.596 |
LIG_BIR_III_4 | 697 | 701 | PF00653 | 0.422 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.466 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.450 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.471 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.655 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.501 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.537 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.502 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.669 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.631 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.460 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.477 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.610 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.395 |
LIG_FHA_2 | 773 | 779 | PF00498 | 0.609 |
LIG_FHA_2 | 799 | 805 | PF00498 | 0.417 |
LIG_GBD_Chelix_1 | 620 | 628 | PF00786 | 0.486 |
LIG_LIR_Apic_2 | 69 | 74 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 773 | 777 | PF02991 | 0.587 |
LIG_LIR_Apic_2 | 810 | 814 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 638 | 645 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 684 | 693 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 638 | 642 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 810 | 816 | PF02991 | 0.473 |
LIG_MLH1_MIPbox_1 | 414 | 418 | PF16413 | 0.568 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.656 |
LIG_PCNA_PIPBox_1 | 805 | 814 | PF02747 | 0.394 |
LIG_PCNA_yPIPBox_3 | 80 | 90 | PF02747 | 0.409 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.468 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.487 |
LIG_REV1ctd_RIR_1 | 397 | 407 | PF16727 | 0.375 |
LIG_SH2_GRB2like | 504 | 507 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 513 | 517 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.554 |
LIG_SH2_SRC | 627 | 630 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 513 | 517 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 831 | 835 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 821 | 824 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 843 | 846 | PF00017 | 0.367 |
LIG_SH3_1 | 543 | 549 | PF00018 | 0.536 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.553 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.405 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.717 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.571 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.533 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.542 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.550 |
LIG_SH3_3 | 811 | 817 | PF00018 | 0.414 |
LIG_SH3_CIN85_PxpxPR_1 | 538 | 543 | PF14604 | 0.554 |
LIG_SUMO_SIM_anti_2 | 313 | 318 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 688 | 694 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 613 | 618 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 647 | 654 | PF11976 | 0.427 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.502 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.437 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.454 |
LIG_WRC_WIRS_1 | 771 | 776 | PF05994 | 0.460 |
LIG_WW_3 | 30 | 34 | PF00397 | 0.583 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.567 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.435 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.598 |
MOD_CK1_1 | 860 | 866 | PF00069 | 0.490 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.598 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.347 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.335 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.565 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.430 |
MOD_CK2_1 | 798 | 804 | PF00069 | 0.441 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.622 |
MOD_Cter_Amidation | 765 | 768 | PF01082 | 0.585 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.321 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.592 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.579 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.379 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.699 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.335 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.658 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.610 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.360 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.621 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.641 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.475 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.398 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.694 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.451 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.565 |
MOD_GSK3_1 | 860 | 867 | PF00069 | 0.540 |
MOD_LATS_1 | 629 | 635 | PF00433 | 0.554 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.624 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.262 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.654 |
MOD_N-GLC_1 | 826 | 831 | PF02516 | 0.536 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.344 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.447 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.280 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.673 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.655 |
MOD_NEK2_1 | 756 | 761 | PF00069 | 0.378 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.566 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.480 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.386 |
MOD_NEK2_2 | 476 | 481 | PF00069 | 0.581 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.545 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.603 |
MOD_PK_1 | 338 | 344 | PF00069 | 0.396 |
MOD_PKA_1 | 497 | 503 | PF00069 | 0.340 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.396 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.351 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.660 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.353 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.669 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.725 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.555 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.709 |
MOD_PKA_2 | 778 | 784 | PF00069 | 0.517 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.320 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.591 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.298 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.344 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.494 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.531 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.690 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.367 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.202 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.601 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.693 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.631 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.290 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.503 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.510 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.514 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.625 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.341 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.662 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.402 |
MOD_SUMO_rev_2 | 561 | 569 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 716 | 726 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 733 | 741 | PF00179 | 0.449 |
TRG_DiLeu_BaEn_1 | 804 | 809 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_2 | 303 | 309 | PF01217 | 0.340 |
TRG_DiLeu_BaEn_4 | 189 | 195 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 842 | 845 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.224 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 788 | 790 | PF00400 | 0.377 |
TRG_NLS_MonoCore_2 | 528 | 533 | PF00514 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 23 | 28 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 734 | 738 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 790 | 794 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 71% | 100% |
A0A0N1HZ98 | Leptomonas seymouri | 22% | 100% |
A0A0N1PBW1 | Leptomonas seymouri | 26% | 100% |
A0A0S4IJW8 | Bodo saltans | 36% | 100% |
A0A1X0NEV8 | Trypanosomatidae | 47% | 100% |
A0A1X0NLI2 | Trypanosomatidae | 24% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 23% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 47% | 100% |
A0A3R7L048 | Trypanosoma rangeli | 24% | 100% |
A0A422NK00 | Trypanosoma rangeli | 26% | 100% |
A4HE78 | Leishmania braziliensis | 22% | 99% |
A4HFK9 | Leishmania braziliensis | 23% | 100% |
A4HTP5 | Leishmania infantum | 99% | 100% |
A4I1J2 | Leishmania infantum | 23% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AD64 | Leishmania major | 22% | 100% |
E9AI34 | Leishmania braziliensis | 87% | 100% |
E9AMI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
Q4Q9U5 | Leishmania major | 23% | 100% |
Q4QI57 | Leishmania major | 96% | 100% |
V5ASV2 | Trypanosoma cruzi | 24% | 100% |
V5D3X9 | Trypanosoma cruzi | 22% | 100% |