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: 30 |
NetGPI | no | yes: 0, no: 31 |
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: E9AMI2
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 | 22 |
GO:0005509 | calcium ion binding | 5 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043169 | cation binding | 3 | 21 |
GO:0046872 | metal ion binding | 4 | 21 |
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 | 0.534 |
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.740 |
CLV_C14_Caspase3-7 | 740 | 744 | PF00656 | 0.520 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.559 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 727 | 729 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 766 | 768 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.396 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.263 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 839 | 841 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.767 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.416 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.413 |
DOC_ANK_TNKS_1 | 291 | 298 | PF00023 | 0.518 |
DOC_CKS1_1 | 473 | 478 | PF01111 | 0.385 |
DOC_CKS1_1 | 781 | 786 | PF01111 | 0.428 |
DOC_CYCLIN_RxL_1 | 431 | 440 | PF00134 | 0.493 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 301 | 307 | PF00134 | 0.503 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 32 | PF00134 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 408 | 414 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 486 | 492 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 546 | 552 | PF00134 | 0.367 |
DOC_MAPK_DCC_7 | 778 | 787 | PF00069 | 0.387 |
DOC_MAPK_FxFP_2 | 810 | 813 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 140 | 146 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 529 | 536 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 644 | 652 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 279 | 286 | PF00149 | 0.439 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 546 | 549 | PF13499 | 0.367 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.531 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.703 |
DOC_PP4_FxxP_1 | 773 | 776 | PF00568 | 0.641 |
DOC_PP4_FxxP_1 | 810 | 813 | PF00568 | 0.352 |
DOC_SPAK_OSR1_1 | 498 | 502 | PF12202 | 0.488 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 856 | 860 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 535 | 539 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.395 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 319 | 329 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 709 | 714 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 754 | 760 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.711 |
LIG_APCC_ABBA_1 | 305 | 310 | PF00400 | 0.490 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.667 |
LIG_BIR_III_4 | 456 | 460 | PF00653 | 0.536 |
LIG_BIR_III_4 | 609 | 613 | PF00653 | 0.588 |
LIG_BIR_III_4 | 697 | 701 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.621 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.544 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.426 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.459 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.457 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.641 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.463 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.648 |
LIG_FHA_1 | 827 | 833 | PF00498 | 0.504 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.348 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.686 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.623 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.440 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.470 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.588 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.361 |
LIG_FHA_2 | 772 | 778 | PF00498 | 0.581 |
LIG_FHA_2 | 798 | 804 | PF00498 | 0.438 |
LIG_GBD_Chelix_1 | 620 | 628 | PF00786 | 0.457 |
LIG_Integrin_RGD_1 | 767 | 769 | PF01839 | 0.402 |
LIG_LIR_Apic_2 | 69 | 74 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 772 | 776 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 809 | 813 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 638 | 645 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 684 | 693 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 638 | 642 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 809 | 815 | PF02991 | 0.455 |
LIG_MLH1_MIPbox_1 | 414 | 418 | PF16413 | 0.544 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.652 |
LIG_PCNA_PIPBox_1 | 804 | 813 | PF02747 | 0.369 |
LIG_PCNA_yPIPBox_3 | 80 | 90 | PF02747 | 0.372 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.428 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.511 |
LIG_REV1ctd_RIR_1 | 397 | 407 | PF16727 | 0.337 |
LIG_SH2_GRB2like | 504 | 507 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 513 | 517 | PF00017 | 0.487 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.540 |
LIG_SH2_SRC | 627 | 630 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 513 | 517 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 830 | 834 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 820 | 823 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 842 | 845 | PF00017 | 0.338 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.544 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.382 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.752 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.543 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.538 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.502 |
LIG_SH3_3 | 778 | 784 | PF00018 | 0.529 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.420 |
LIG_SH3_CIN85_PxpxPR_1 | 538 | 543 | PF14604 | 0.540 |
LIG_SUMO_SIM_anti_2 | 313 | 318 | PF11976 | 0.439 |
LIG_SUMO_SIM_anti_2 | 688 | 694 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 613 | 618 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 647 | 654 | PF11976 | 0.401 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.478 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.417 |
LIG_WRC_WIRS_1 | 770 | 775 | PF05994 | 0.428 |
LIG_WW_3 | 30 | 34 | PF00397 | 0.565 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.416 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.556 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.570 |
MOD_CK1_1 | 814 | 820 | PF00069 | 0.566 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.564 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.311 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.669 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.303 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.521 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.401 |
MOD_CK2_1 | 797 | 803 | PF00069 | 0.450 |
MOD_Cter_Amidation | 764 | 767 | PF01082 | 0.569 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.304 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.597 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.542 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.343 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.732 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.310 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.568 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.651 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.443 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.584 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.325 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.595 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.626 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.571 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.445 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.376 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.676 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.410 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.512 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.349 |
MOD_LATS_1 | 629 | 635 | PF00433 | 0.525 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.605 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.224 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.607 |
MOD_N-GLC_1 | 825 | 830 | PF02516 | 0.524 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.305 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.224 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.571 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.256 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.634 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.651 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.348 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.484 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.456 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.347 |
MOD_NEK2_2 | 476 | 481 | PF00069 | 0.364 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.499 |
MOD_PIKK_1 | 818 | 824 | PF00454 | 0.621 |
MOD_PK_1 | 338 | 344 | PF00069 | 0.364 |
MOD_PK_1 | 704 | 710 | PF00069 | 0.444 |
MOD_PKA_1 | 497 | 503 | PF00069 | 0.329 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.364 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.316 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.625 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.319 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.619 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.700 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.563 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.706 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.480 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.639 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.294 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.553 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.294 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.336 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.503 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.515 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.663 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.392 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.309 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.584 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.674 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.540 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.500 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.475 |
MOD_Plk_4 | 845 | 851 | PF00069 | 0.621 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.647 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.393 |
MOD_SUMO_rev_2 | 561 | 569 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 715 | 725 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 732 | 740 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 803 | 808 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_2 | 303 | 309 | PF01217 | 0.304 |
TRG_DiLeu_BaEn_4 | 189 | 195 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 841 | 844 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.374 |
TRG_NLS_MonoCore_2 | 528 | 533 | PF00514 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 733 | 737 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 789 | 793 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 70% | 100% |
A0A0N1HZ98 | Leptomonas seymouri | 22% | 100% |
A0A0N1I3M2 | Leptomonas seymouri | 23% | 100% |
A0A0N1PBW1 | Leptomonas seymouri | 24% | 100% |
A0A0S4IJW8 | Bodo saltans | 35% | 100% |
A0A0S4IQM0 | Bodo saltans | 25% | 100% |
A0A1X0NEV8 | Trypanosomatidae | 46% | 100% |
A0A1X0NLI2 | Trypanosomatidae | 23% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 23% | 100% |
A0A3Q8IPU3 | Leishmania donovani | 23% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 47% | 100% |
A0A3R7L048 | Trypanosoma rangeli | 24% | 100% |
A0A3S5H688 | Leishmania donovani | 95% | 99% |
A0A422NK00 | Trypanosoma rangeli | 26% | 100% |
A4HE78 | Leishmania braziliensis | 22% | 99% |
A4HFK9 | Leishmania braziliensis | 23% | 97% |
A4HTP5 | Leishmania infantum | 94% | 99% |
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% |
E9AD64 | Leishmania major | 23% | 100% |
E9AHF6 | Leishmania infantum | 23% | 100% |
E9AI34 | Leishmania braziliensis | 88% | 100% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
Q4Q9U5 | Leishmania major | 24% | 100% |
Q4QI57 | Leishmania major | 94% | 100% |
V5ASV2 | Trypanosoma cruzi | 24% | 100% |
V5D3X9 | Trypanosoma cruzi | 23% | 100% |