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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0016020 | membrane | 2 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJ42
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 1 |
GO:0000963 | mitochondrial RNA processing | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010467 | gene expression | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016553 | base conversion or substitution editing | 6 | 1 |
GO:0016554 | cytidine to uridine editing | 7 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140053 | mitochondrial gene expression | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.603 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.692 |
CLV_PCSK_FUR_1 | 510 | 514 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 679 | 681 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 700 | 702 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 741 | 743 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 105 | 111 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 846 | 850 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 851 | 855 | PF00082 | 0.441 |
DEG_APCC_DBOX_1 | 413 | 421 | PF00400 | 0.435 |
DEG_APCC_DBOX_1 | 814 | 822 | PF00400 | 0.536 |
DEG_APCC_DBOX_1 | 850 | 858 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 895 | 903 | PF00400 | 0.471 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.701 |
DEG_SCF_FBW7_2 | 688 | 693 | PF00400 | 0.559 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.482 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.462 |
DOC_CDC14_PxL_1 | 4 | 12 | PF14671 | 0.761 |
DOC_CDC14_PxL_1 | 841 | 849 | PF14671 | 0.574 |
DOC_CYCLIN_RxL_1 | 785 | 796 | PF00134 | 0.560 |
DOC_CYCLIN_RxL_1 | 846 | 855 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 543 | 549 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 806 | 812 | PF00134 | 0.606 |
DOC_MAPK_DCC_7 | 541 | 549 | PF00069 | 0.436 |
DOC_MAPK_DCC_7 | 802 | 812 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 355 | 361 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 568 | 578 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 651 | 660 | PF00069 | 0.679 |
DOC_MAPK_gen_1 | 679 | 685 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 700 | 708 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 741 | 747 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 856 | 865 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 915 | 924 | PF00069 | 0.507 |
DOC_MAPK_JIP1_4 | 545 | 551 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 701 | 710 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 842 | 849 | PF00069 | 0.319 |
DOC_MAPK_RevD_3 | 399 | 414 | PF00069 | 0.448 |
DOC_PP1_RVXF_1 | 355 | 362 | PF00149 | 0.433 |
DOC_PP1_RVXF_1 | 788 | 794 | PF00149 | 0.306 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.488 |
DOC_PP4_FxxP_1 | 532 | 535 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 555 | 558 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.521 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 894 | 899 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 431 | 440 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 497 | 502 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 562 | 570 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 571 | 578 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 931 | 938 | PF00244 | 0.622 |
LIG_14-3-3_CterR_2 | 941 | 944 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 172 | 190 | PF00022 | 0.416 |
LIG_APCC_ABBA_1 | 328 | 333 | PF00400 | 0.343 |
LIG_APCC_ABBA_1 | 716 | 721 | PF00400 | 0.290 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.541 |
LIG_EH1_1 | 214 | 222 | PF00400 | 0.405 |
LIG_EVH1_2 | 556 | 560 | PF00568 | 0.431 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.548 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.674 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.371 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.422 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.365 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.559 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.563 |
LIG_FHA_1 | 867 | 873 | PF00498 | 0.599 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.560 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.468 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.520 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.495 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.733 |
LIG_FHA_2 | 712 | 718 | PF00498 | 0.418 |
LIG_FHA_2 | 881 | 887 | PF00498 | 0.455 |
LIG_FHA_2 | 895 | 901 | PF00498 | 0.432 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.512 |
LIG_LIR_Apic_2 | 375 | 379 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 427 | 437 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 445 | 456 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 523 | 532 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 559 | 566 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 619 | 629 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 717 | 724 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 774 | 784 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 786 | 793 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 889 | 898 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 439 | 443 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 619 | 624 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 717 | 722 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 774 | 780 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 786 | 791 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 889 | 893 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.588 |
LIG_Pex14_2 | 793 | 797 | PF04695 | 0.328 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.504 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.504 |
LIG_SH2_CRK | 803 | 807 | PF00017 | 0.638 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.713 |
LIG_SH2_NCK_1 | 448 | 452 | PF00017 | 0.353 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.281 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 776 | 779 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.455 |
LIG_SH3_1 | 413 | 419 | PF00018 | 0.558 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.540 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.558 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.708 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.512 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.528 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.508 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.716 |
LIG_SUMO_SIM_anti_2 | 189 | 197 | PF11976 | 0.551 |
LIG_SUMO_SIM_anti_2 | 707 | 712 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 822 | 828 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 194 | 201 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 218 | 225 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 689 | 697 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 709 | 714 | PF11976 | 0.204 |
LIG_SUMO_SIM_par_1 | 920 | 926 | PF11976 | 0.339 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.457 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.752 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.383 |
LIG_TRAF2_1 | 475 | 478 | PF00917 | 0.701 |
LIG_TRAF2_1 | 48 | 51 | PF00917 | 0.617 |
LIG_TRAF2_1 | 637 | 640 | PF00917 | 0.739 |
LIG_TRAF2_1 | 923 | 926 | PF00917 | 0.387 |
LIG_UBA3_1 | 853 | 859 | PF00899 | 0.568 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.428 |
LIG_WRC_WIRS_1 | 887 | 892 | PF05994 | 0.450 |
LIG_WRC_WIRS_1 | 908 | 913 | PF05994 | 0.283 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.564 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.703 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.484 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.628 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.359 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.410 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.610 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.642 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.398 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.435 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.597 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.468 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.669 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.645 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.516 |
MOD_CK2_1 | 849 | 855 | PF00069 | 0.495 |
MOD_CK2_1 | 886 | 892 | PF00069 | 0.545 |
MOD_CK2_1 | 920 | 926 | PF00069 | 0.516 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.723 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.598 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.703 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.601 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.456 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.369 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.644 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.493 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.567 |
MOD_GlcNHglycan | 647 | 651 | PF01048 | 0.700 |
MOD_GlcNHglycan | 730 | 734 | PF01048 | 0.425 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.748 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.611 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.412 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.580 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.615 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.568 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.536 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.598 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.599 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.551 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.488 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.509 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.644 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.544 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.498 |
MOD_GSK3_1 | 926 | 933 | PF00069 | 0.513 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.439 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.640 |
MOD_N-GLC_1 | 643 | 648 | PF02516 | 0.627 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.436 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.729 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.436 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.501 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.530 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.601 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.379 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.419 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.470 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.463 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.248 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.773 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.596 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.533 |
MOD_PIKK_1 | 711 | 717 | PF00454 | 0.534 |
MOD_PIKK_1 | 936 | 942 | PF00454 | 0.511 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.721 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.456 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.696 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.458 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.647 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.395 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.734 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.405 |
MOD_PKA_2 | 930 | 936 | PF00069 | 0.605 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.718 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.358 |
MOD_Plk_2-3 | 886 | 892 | PF00069 | 0.312 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.458 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.450 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.441 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.566 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.402 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.336 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.426 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.609 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.575 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.666 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.540 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.638 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.470 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.537 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.606 |
MOD_ProDKin_1 | 894 | 900 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 452 | 462 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 477 | 484 | PF00179 | 0.723 |
MOD_SUMO_rev_2 | 923 | 929 | PF00179 | 0.391 |
MOD_SUMO_rev_2 | 99 | 103 | PF00179 | 0.593 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 602 | 607 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 868 | 873 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_4 | 457 | 463 | PF01217 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 687 | 692 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.714 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 43 | 45 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 510 | 513 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 652 | 655 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 662 | 665 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 730 | 744 | PF08389 | 0.315 |
TRG_NES_CRM1_1 | 817 | 828 | PF08389 | 0.405 |
TRG_NLS_Bipartite_1 | 92 | 112 | PF00514 | 0.706 |
TRG_NLS_MonoExtC_3 | 107 | 113 | PF00514 | 0.652 |
TRG_NLS_MonoExtC_3 | 261 | 267 | PF00514 | 0.445 |
TRG_NLS_MonoExtN_4 | 105 | 112 | PF00514 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 441 | 445 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 851 | 855 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG9 | Leptomonas seymouri | 58% | 98% |
A0A1X0NJ60 | Trypanosomatidae | 43% | 100% |
A0A3Q8IF71 | Leishmania donovani | 79% | 96% |
A0A3S5IRN6 | Trypanosoma rangeli | 42% | 100% |
A4I6F7 | Leishmania infantum | 79% | 93% |
C9ZN75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZWW8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B1L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 97% |
Q4Q6K0 | Leishmania major | 80% | 100% |