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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005819 | spindle | 5 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0072686 | mitotic spindle | 6 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XC76
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.208 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.344 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.254 |
CLV_PCSK_FUR_1 | 508 | 512 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 617 | 623 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 728 | 736 | PF00400 | 0.389 |
DEG_SCF_FBW7_2 | 365 | 371 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 553 | 557 | PF00917 | 0.494 |
DOC_ANK_TNKS_1 | 141 | 148 | PF00023 | 0.475 |
DOC_CDC14_PxL_1 | 9 | 17 | PF14671 | 0.441 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.450 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.437 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.392 |
DOC_CKS1_1 | 700 | 705 | PF01111 | 0.563 |
DOC_CKS1_1 | 717 | 722 | PF01111 | 0.346 |
DOC_CYCLIN_RxL_1 | 656 | 665 | PF00134 | 0.385 |
DOC_CYCLIN_RxL_1 | 725 | 734 | PF00134 | 0.408 |
DOC_CYCLIN_yClb1_LxF_4 | 250 | 256 | PF00134 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.391 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 261 | 268 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 296 | 308 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 486 | 495 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 263 | 269 | PF00149 | 0.511 |
DOC_PP1_RVXF_1 | 734 | 741 | PF00149 | 0.339 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 460 | 463 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.422 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.375 |
DOC_USP7_UBL2_3 | 697 | 701 | PF12436 | 0.520 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.330 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 659 | 664 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 667 | 671 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 673 | 683 | PF00244 | 0.305 |
LIG_Actin_WH2_2 | 474 | 490 | PF00022 | 0.511 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BIR_III_4 | 390 | 394 | PF00653 | 0.487 |
LIG_BRCT_BRCA1_1 | 545 | 549 | PF00533 | 0.278 |
LIG_deltaCOP1_diTrp_1 | 593 | 601 | PF00928 | 0.490 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.454 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.425 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.410 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.581 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.490 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.421 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.376 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.574 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.409 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.524 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.475 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.436 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.481 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.633 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.565 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.418 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.434 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.384 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.511 |
LIG_IRF3_LxIS_1 | 605 | 612 | PF10401 | 0.431 |
LIG_LIR_Apic_2 | 336 | 341 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 19 | 27 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 509 | 520 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 593 | 601 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 593 | 598 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.438 |
LIG_PDZ_Class_2 | 736 | 741 | PF00595 | 0.369 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.514 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.408 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.408 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.418 |
LIG_Pex14_2 | 601 | 605 | PF04695 | 0.362 |
LIG_Pex14_2 | 610 | 614 | PF04695 | 0.466 |
LIG_Rb_pABgroove_1 | 273 | 281 | PF01858 | 0.511 |
LIG_SH2_CRK | 717 | 721 | PF00017 | 0.476 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.421 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.420 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.475 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.531 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 120 | 126 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 274 | 280 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 333 | 339 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 452 | 459 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 668 | 674 | PF11976 | 0.477 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.511 |
LIG_TRAF2_1 | 731 | 734 | PF00917 | 0.477 |
LIG_TYR_ITIM | 164 | 169 | PF00017 | 0.403 |
LIG_UBA3_1 | 501 | 510 | PF00899 | 0.478 |
LIG_WRC_WIRS_1 | 672 | 677 | PF05994 | 0.482 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.400 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.438 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.511 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.410 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.434 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.391 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.546 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.458 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.488 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.408 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.573 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.418 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.641 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.468 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.322 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.357 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.387 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.408 |
MOD_Cter_Amidation | 29 | 32 | PF01082 | 0.532 |
MOD_Cter_Amidation | 377 | 380 | PF01082 | 0.622 |
MOD_Cter_Amidation | 395 | 398 | PF01082 | 0.549 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.208 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.445 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.634 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.559 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.208 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.591 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.492 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.554 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.399 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.416 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.419 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.503 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.409 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.568 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.437 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.475 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.443 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.582 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.432 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.121 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.650 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.406 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.627 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.552 |
MOD_NEK2_2 | 671 | 676 | PF00069 | 0.462 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.371 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.574 |
MOD_PIKK_1 | 616 | 622 | PF00454 | 0.672 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.555 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.370 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.618 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.399 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.407 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.614 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.494 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.408 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.477 |
MOD_Plk_2-3 | 453 | 459 | PF00069 | 0.418 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.462 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.445 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.422 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.513 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.508 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.418 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.420 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.460 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.485 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.408 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.404 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.581 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.568 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.336 |
MOD_SUMO_rev_2 | 78 | 87 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_1 | 708 | 713 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 728 | 730 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 735 | 737 | PF00400 | 0.336 |
TRG_NLS_MonoExtC_3 | 378 | 383 | PF00514 | 0.549 |
TRG_NLS_MonoExtN_4 | 106 | 112 | PF00514 | 0.418 |
TRG_NLS_MonoExtN_4 | 261 | 266 | PF00514 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 728 | 733 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ98 | Leptomonas seymouri | 27% | 96% |
A0A0N1I3M2 | Leptomonas seymouri | 26% | 97% |
A0A0N1PBW1 | Leptomonas seymouri | 72% | 99% |
A0A0S4IQM0 | Bodo saltans | 39% | 100% |
A0A0S4J8J7 | Bodo saltans | 26% | 81% |
A0A1X0NEV8 | Trypanosomatidae | 27% | 93% |
A0A1X0NLI2 | Trypanosomatidae | 50% | 100% |
A0A1X0NMQ3 | Trypanosomatidae | 28% | 95% |
A0A1X0P419 | Trypanosomatidae | 25% | 98% |
A0A3Q1N1R0 | Bos taurus | 25% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 27% | 100% |
A0A3Q8IPU3 | Leishmania donovani | 27% | 99% |
A0A3R7KM50 | Trypanosoma rangeli | 26% | 93% |
A0A3R7L048 | Trypanosoma rangeli | 27% | 98% |
A0A422N0Z6 | Trypanosoma rangeli | 27% | 95% |
A0A422NK00 | Trypanosoma rangeli | 52% | 100% |
A4HE78 | Leishmania braziliensis | 27% | 100% |
A4HFK9 | Leishmania braziliensis | 26% | 100% |
A4HQF8 | Leishmania braziliensis | 87% | 100% |
A4I1J2 | Leishmania infantum | 27% | 100% |
A4IC94 | Leishmania infantum | 99% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 92% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 95% |
D0A3K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 99% |
E1BKH1 | Bos taurus | 28% | 100% |
E9AD64 | Leishmania major | 27% | 98% |
E9AHF6 | Leishmania infantum | 27% | 99% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 96% |
Q32TF8 | Danio rerio | 27% | 99% |
Q32TG3 | Gallus gallus | 26% | 99% |
Q4Q0C0 | Leishmania major | 96% | 100% |
Q4Q9U5 | Leishmania major | 26% | 100% |
Q5JST6 | Homo sapiens | 25% | 99% |
Q9D485 | Mus musculus | 24% | 99% |
Q9D9T8 | Mus musculus | 29% | 100% |
V5ASV2 | Trypanosoma cruzi | 51% | 100% |
V5D3X9 | Trypanosoma cruzi | 26% | 95% |
V5DA42 | Trypanosoma cruzi | 27% | 98% |