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. | yes | yes: 20 |
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:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005643 | nuclear pore | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HAG4
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006913 | nucleocytoplasmic transport | 5 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0034504 | protein localization to nucleus | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051169 | nuclear transport | 4 | 12 |
GO:0051170 | import into nucleus | 6 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0019899 | enzyme binding | 3 | 11 |
GO:0031267 | small GTPase binding | 5 | 11 |
GO:0051020 | GTPase binding | 4 | 11 |
GO:0005048 | signal sequence binding | 4 | 1 |
GO:0008139 | nuclear localization sequence binding | 5 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
GO:0061608 | nuclear import signal receptor activity | 3 | 1 |
GO:0140104 | molecular carrier activity | 1 | 1 |
GO:0140142 | nucleocytoplasmic carrier activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 772 | 776 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 829 | 833 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 855 | 859 | PF00082 | 0.632 |
DEG_APCC_DBOX_1 | 860 | 868 | PF00400 | 0.576 |
DEG_ODPH_VHL_1 | 777 | 789 | PF01847 | 0.451 |
DOC_CKS1_1 | 443 | 448 | PF01111 | 0.541 |
DOC_MAPK_gen_1 | 377 | 386 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 584 | 593 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 495 | 504 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 550 | 557 | PF00069 | 0.385 |
DOC_PP4_FxxP_1 | 649 | 652 | PF00568 | 0.599 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.475 |
DOC_USP7_UBL2_3 | 854 | 858 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 495 | 504 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 734 | 741 | PF00244 | 0.548 |
LIG_Actin_WH2_2 | 402 | 419 | PF00022 | 0.557 |
LIG_Actin_WH2_2 | 50 | 65 | PF00022 | 0.392 |
LIG_Actin_WH2_2 | 830 | 848 | PF00022 | 0.366 |
LIG_AP2alpha_1 | 438 | 442 | PF02296 | 0.391 |
LIG_APCC_ABBA_1 | 590 | 595 | PF00400 | 0.527 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 714 | 718 | PF00533 | 0.562 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.469 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.412 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.413 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.407 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.498 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.482 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.473 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.478 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.534 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.476 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.574 |
LIG_FHA_1 | 832 | 838 | PF00498 | 0.384 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.540 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.561 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.471 |
LIG_FHA_2 | 659 | 665 | PF00498 | 0.330 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.489 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.585 |
LIG_FHA_2 | 847 | 853 | PF00498 | 0.597 |
LIG_GBD_Chelix_1 | 112 | 120 | PF00786 | 0.440 |
LIG_Integrin_RGD_1 | 742 | 744 | PF01839 | 0.645 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 436 | 446 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 494 | 505 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 653 | 662 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 683 | 693 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 703 | 713 | PF02991 | 0.206 |
LIG_LIR_Gen_1 | 760 | 769 | PF02991 | 0.423 |
LIG_LIR_LC3C_4 | 498 | 502 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 436 | 441 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 703 | 708 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 715 | 721 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 760 | 765 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.316 |
LIG_MYND_1 | 723 | 727 | PF01753 | 0.441 |
LIG_PCNA_yPIPBox_3 | 517 | 528 | PF02747 | 0.477 |
LIG_PCNA_yPIPBox_3 | 838 | 846 | PF02747 | 0.362 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.380 |
LIG_Pex14_2 | 701 | 705 | PF04695 | 0.471 |
LIG_PTB_Apo_2 | 679 | 686 | PF02174 | 0.535 |
LIG_PTB_Phospho_1 | 679 | 685 | PF10480 | 0.528 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.416 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.530 |
LIG_SH2_CRK | 656 | 660 | PF00017 | 0.542 |
LIG_SH2_CRK | 762 | 766 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.557 |
LIG_SH2_GRB2like | 685 | 688 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 656 | 660 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 762 | 766 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 685 | 688 | PF00017 | 0.573 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.316 |
LIG_SH2_STAT3 | 310 | 313 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 539 | 542 | PF00017 | 0.589 |
LIG_SH2_STAT3 | 611 | 614 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 750 | 753 | PF00017 | 0.412 |
LIG_SH3_1 | 717 | 723 | PF00018 | 0.444 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.525 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.315 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.444 |
LIG_SH3_3 | 816 | 822 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 498 | 505 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 603 | 608 | PF11976 | 0.577 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.560 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.512 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.509 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.505 |
LIG_TYR_ITIM | 253 | 258 | PF00017 | 0.494 |
LIG_UBA3_1 | 133 | 142 | PF00899 | 0.334 |
LIG_UBA3_1 | 412 | 420 | PF00899 | 0.326 |
LIG_WRC_WIRS_1 | 34 | 39 | PF05994 | 0.478 |
LIG_WRC_WIRS_1 | 784 | 789 | PF05994 | 0.498 |
LIG_WRPW_2 | 718 | 721 | PF00400 | 0.560 |
MOD_CDC14_SPxK_1 | 104 | 107 | PF00782 | 0.504 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.392 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.522 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.420 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.622 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.519 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.567 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.450 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.382 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.500 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.455 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.562 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.459 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.497 |
MOD_CK2_1 | 793 | 799 | PF00069 | 0.501 |
MOD_CK2_1 | 845 | 851 | PF00069 | 0.660 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.570 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.441 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.357 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.329 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.521 |
MOD_GlcNHglycan | 425 | 429 | PF01048 | 0.439 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.611 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.617 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.486 |
MOD_GlcNHglycan | 606 | 610 | PF01048 | 0.484 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.433 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.415 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.240 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.527 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.478 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.538 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.485 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.453 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.451 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.305 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.395 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.551 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.414 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.630 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.547 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.441 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.587 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.576 |
MOD_N-GLC_1 | 793 | 798 | PF02516 | 0.400 |
MOD_N-GLC_1 | 817 | 822 | PF02516 | 0.380 |
MOD_N-GLC_2 | 232 | 234 | PF02516 | 0.338 |
MOD_N-GLC_2 | 533 | 535 | PF02516 | 0.470 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.523 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.425 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.374 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.564 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.370 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.443 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.448 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.592 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.378 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.497 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.441 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.410 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.388 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.386 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.491 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.623 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.341 |
MOD_OFUCOSY | 699 | 704 | PF10250 | 0.505 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.326 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.427 |
MOD_PIKK_1 | 763 | 769 | PF00454 | 0.481 |
MOD_PIKK_1 | 798 | 804 | PF00454 | 0.543 |
MOD_PK_1 | 379 | 385 | PF00069 | 0.528 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.525 |
MOD_PKA_2 | 733 | 739 | PF00069 | 0.559 |
MOD_PKA_2 | 845 | 851 | PF00069 | 0.407 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.536 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.440 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.422 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.528 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.500 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.429 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.553 |
MOD_Plk_1 | 663 | 669 | PF00069 | 0.404 |
MOD_Plk_1 | 798 | 804 | PF00069 | 0.515 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.561 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.421 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.449 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.528 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.514 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.280 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.392 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.416 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.273 |
MOD_Plk_4 | 757 | 763 | PF00069 | 0.407 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.403 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.384 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 94 | 97 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 190 | 198 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 414 | 422 | PF00179 | 0.334 |
MOD_SUMO_rev_2 | 44 | 52 | PF00179 | 0.374 |
MOD_SUMO_rev_2 | 509 | 519 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 692 | 700 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 821 | 831 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_4 | 277 | 283 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 762 | 765 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.554 |
TRG_NES_CRM1_1 | 589 | 603 | PF08389 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 84 | 89 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB22 | Leptomonas seymouri | 77% | 100% |
A0A0S4J2L0 | Bodo saltans | 48% | 100% |
A0A1X0P8K4 | Trypanosomatidae | 53% | 100% |
A0A3Q8IUD8 | Leishmania donovani | 89% | 100% |
A0A3R7LLX8 | Trypanosoma rangeli | 51% | 100% |
A4I9L9 | Leishmania infantum | 88% | 100% |
D0A1Y4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B4L7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O00410 | Homo sapiens | 21% | 79% |
O13864 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
O18388 | Drosophila melanogaster | 27% | 98% |
P52296 | Rattus norvegicus | 28% | 99% |
P52297 | Xenopus laevis | 28% | 99% |
P70168 | Mus musculus | 29% | 99% |
Q06142 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
Q14974 | Homo sapiens | 29% | 99% |
Q3SYU7 | Bos taurus | 21% | 97% |
Q4Q3F9 | Leishmania major | 88% | 100% |
Q8BFY9 | Mus musculus | 21% | 97% |
Q8BKC5 | Mus musculus | 21% | 79% |
Q8H0U4 | Arabidopsis thaliana | 21% | 98% |
Q92973 | Homo sapiens | 21% | 97% |
Q9FJD4 | Arabidopsis thaliana | 30% | 100% |
V5BHR5 | Trypanosoma cruzi | 48% | 100% |