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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
GO:0005680 | anaphase-promoting complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AY19
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007088 | regulation of mitotic nuclear division | 6 | 1 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010638 | positive regulation of organelle organization | 6 | 1 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0030071 | regulation of mitotic metaphase/anaphase transition | 7 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033044 | regulation of chromosome organization | 6 | 1 |
GO:0033045 | regulation of sister chromatid segregation | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044784 | metaphase/anaphase transition of cell cycle | 4 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0045840 | positive regulation of mitotic nuclear division | 7 | 1 |
GO:0045842 | positive regulation of mitotic metaphase/anaphase transition | 8 | 1 |
GO:0045931 | positive regulation of mitotic cell cycle | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051130 | positive regulation of cellular component organization | 5 | 1 |
GO:0051301 | cell division | 2 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051783 | regulation of nuclear division | 6 | 1 |
GO:0051785 | positive regulation of nuclear division | 7 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901970 | positive regulation of mitotic sister chromatid separation | 7 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901989 | positive regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901992 | positive regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902099 | regulation of metaphase/anaphase transition of cell cycle | 6 | 1 |
GO:1902101 | positive regulation of metaphase/anaphase transition of cell cycle | 7 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1905818 | regulation of chromosome separation | 5 | 1 |
GO:1905820 | positive regulation of chromosome separation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 240 | 244 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 800 | 802 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 792 | 796 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 797 | 801 | PF00082 | 0.312 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.594 |
DEG_SPOP_SBC_1 | 532 | 536 | PF00917 | 0.586 |
DOC_CKS1_1 | 483 | 488 | PF01111 | 0.550 |
DOC_CKS1_1 | 674 | 679 | PF01111 | 0.340 |
DOC_CYCLIN_RxL_1 | 172 | 184 | PF00134 | 0.556 |
DOC_CYCLIN_RxL_1 | 599 | 608 | PF00134 | 0.430 |
DOC_CYCLIN_RxL_1 | 789 | 798 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 172 | 181 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 265 | 275 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 557 | 566 | PF00069 | 0.430 |
DOC_MAPK_HePTP_8 | 343 | 355 | PF00069 | 0.444 |
DOC_MAPK_HePTP_8 | 554 | 566 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 346 | 355 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 557 | 566 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 447 | 454 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 600 | 607 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 769 | 772 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 837 | 840 | PF13499 | 0.435 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.291 |
LIG_14-3-3_CanoR_1 | 15 | 25 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 476 | 483 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 624 | 633 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 648 | 654 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 692 | 700 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 792 | 797 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.417 |
LIG_BIR_III_2 | 224 | 228 | PF00653 | 0.383 |
LIG_eIF4E_1 | 681 | 687 | PF01652 | 0.312 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.562 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.423 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.519 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.415 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.394 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.652 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.325 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.332 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.261 |
LIG_FHA_1 | 844 | 850 | PF00498 | 0.462 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.369 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.472 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.466 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.685 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.312 |
LIG_FHA_2 | 823 | 829 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 689 | 697 | PF00786 | 0.388 |
LIG_LIR_Apic_2 | 828 | 833 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 146 | 155 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 421 | 432 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 756 | 765 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 784 | 794 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 831 | 840 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 756 | 760 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 784 | 789 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 831 | 837 | PF02991 | 0.472 |
LIG_PDZ_Class_3 | 848 | 853 | PF00595 | 0.560 |
LIG_REV1ctd_RIR_1 | 451 | 459 | PF16727 | 0.400 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.388 |
LIG_SH2_CRK | 744 | 748 | PF00017 | 0.402 |
LIG_SH2_CRK | 757 | 761 | PF00017 | 0.242 |
LIG_SH2_NCK_1 | 802 | 806 | PF00017 | 0.312 |
LIG_SH2_NCK_1 | 830 | 834 | PF00017 | 0.455 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.465 |
LIG_SH2_SRC | 42 | 45 | PF00017 | 0.461 |
LIG_SH2_SRC | 612 | 615 | PF00017 | 0.455 |
LIG_SH2_SRC | 681 | 684 | PF00017 | 0.388 |
LIG_SH2_SRC | 750 | 753 | PF00017 | 0.388 |
LIG_SH2_SRC | 802 | 805 | PF00017 | 0.312 |
LIG_SH2_SRC | 99 | 102 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 750 | 754 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 802 | 806 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 643 | 646 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.312 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.714 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.766 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.590 |
LIG_SH3_3 | 762 | 768 | PF00018 | 0.293 |
LIG_SH3_3 | 846 | 852 | PF00018 | 0.622 |
LIG_SUMO_SIM_anti_2 | 235 | 240 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 562 | 567 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 845 | 851 | PF11976 | 0.480 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.395 |
LIG_TRAF2_1 | 840 | 843 | PF00917 | 0.485 |
LIG_TRAF2_1 | 848 | 851 | PF00917 | 0.569 |
LIG_TYR_ITIM | 832 | 837 | PF00017 | 0.473 |
MOD_CDK_SPK_2 | 501 | 506 | PF00069 | 0.603 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.640 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.357 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.457 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.604 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.735 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.725 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.575 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.470 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.515 |
MOD_CK1_1 | 778 | 784 | PF00069 | 0.221 |
MOD_CK1_1 | 815 | 821 | PF00069 | 0.562 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.332 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.423 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.451 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.464 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.698 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.604 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.537 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.243 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.311 |
MOD_CK2_1 | 792 | 798 | PF00069 | 0.312 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.312 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.501 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.715 |
MOD_GlcNHglycan | 517 | 521 | PF01048 | 0.713 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.446 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.425 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.340 |
MOD_GlcNHglycan | 816 | 820 | PF01048 | 0.463 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.376 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.368 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.634 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.479 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.370 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.396 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.655 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.717 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.650 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.596 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.470 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.291 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.327 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.471 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.676 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.345 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.386 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.488 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.444 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.534 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.588 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.520 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.548 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.680 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.469 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.481 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.374 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.482 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.684 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.548 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.494 |
MOD_PK_1 | 341 | 347 | PF00069 | 0.431 |
MOD_PK_1 | 512 | 518 | PF00069 | 0.597 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.434 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.582 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.521 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.584 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.495 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.340 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.358 |
MOD_PKB_1 | 474 | 482 | PF00069 | 0.513 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.431 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.387 |
MOD_Plk_1 | 775 | 781 | PF00069 | 0.207 |
MOD_Plk_1 | 842 | 848 | PF00069 | 0.518 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.374 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.401 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.389 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.371 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.748 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.674 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.653 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.543 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.291 |
MOD_SUMO_for_1 | 523 | 526 | PF00179 | 0.679 |
MOD_SUMO_rev_2 | 167 | 177 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 507 | 514 | PF00179 | 0.616 |
TRG_DiLeu_BaEn_1 | 206 | 211 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_4 | 720 | 726 | PF01217 | 0.591 |
TRG_DiLeu_LyEn_5 | 720 | 725 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 744 | 747 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 757 | 760 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 834 | 837 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.432 |
TRG_NLS_MonoExtC_3 | 240 | 246 | PF00514 | 0.441 |
TRG_NLS_MonoExtN_4 | 172 | 179 | PF00514 | 0.396 |
TRG_NLS_MonoExtN_4 | 240 | 245 | PF00514 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 542 | 547 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P507 | Leptomonas seymouri | 50% | 100% |
A0A3Q8IDI5 | Leishmania donovani | 90% | 100% |
A4HEP3 | Leishmania braziliensis | 73% | 100% |
A4I1X3 | Leishmania infantum | 90% | 100% |
Q4Q9F4 | Leishmania major | 90% | 100% |