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: A4HEP3
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 | 464 | 468 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 655 | 659 | PF00656 | 0.317 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 797 | 799 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 797 | 799 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 794 | 798 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.303 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.320 |
DEG_SCF_SKP2-CKS1_1 | 300 | 307 | PF00560 | 0.484 |
DOC_CYCLIN_RxL_1 | 174 | 186 | PF00134 | 0.564 |
DOC_CYCLIN_RxL_1 | 596 | 605 | PF00134 | 0.455 |
DOC_CYCLIN_RxL_1 | 786 | 795 | PF00134 | 0.312 |
DOC_CYCLIN_yClb1_LxF_4 | 81 | 86 | PF00134 | 0.327 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 766 | 772 | PF00134 | 0.231 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 267 | 277 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 521 | 527 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.484 |
DOC_MAPK_HePTP_8 | 345 | 357 | PF00069 | 0.468 |
DOC_MAPK_HePTP_8 | 551 | 563 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 270 | 279 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 554 | 563 | PF00069 | 0.640 |
DOC_MAPK_NFAT4_5 | 270 | 278 | PF00069 | 0.293 |
DOC_PP1_RVXF_1 | 597 | 604 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 81 | 87 | PF00149 | 0.319 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 766 | 769 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 834 | 837 | PF13499 | 0.432 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 778 | 782 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.508 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.280 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 370 | 379 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 396 | 406 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 457 | 465 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 522 | 528 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 531 | 537 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 759 | 766 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 779 | 784 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 789 | 794 | PF00244 | 0.302 |
LIG_Actin_WH2_2 | 324 | 342 | PF00022 | 0.338 |
LIG_Actin_WH2_2 | 95 | 111 | PF00022 | 0.297 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.482 |
LIG_BRCT_BRCA1_1 | 476 | 480 | PF00533 | 0.504 |
LIG_eIF4E_1 | 596 | 602 | PF01652 | 0.293 |
LIG_eIF4E_1 | 678 | 684 | PF01652 | 0.363 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.415 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.461 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.571 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.484 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.541 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.503 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.425 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.626 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.389 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.419 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.406 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.513 |
LIG_FHA_1 | 765 | 771 | PF00498 | 0.261 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.366 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.356 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.398 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.474 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.349 |
LIG_FHA_2 | 790 | 796 | PF00498 | 0.312 |
LIG_FHA_2 | 820 | 826 | PF00498 | 0.459 |
LIG_GBD_Chelix_1 | 686 | 694 | PF00786 | 0.465 |
LIG_LIR_Apic_2 | 825 | 830 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 423 | 434 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 753 | 758 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 828 | 839 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 753 | 757 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 781 | 786 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 828 | 834 | PF02991 | 0.473 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.443 |
LIG_SH2_CRK | 680 | 684 | PF00017 | 0.430 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.402 |
LIG_SH2_CRK | 754 | 758 | PF00017 | 0.242 |
LIG_SH2_GRB2like | 44 | 47 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 596 | 599 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 799 | 803 | PF00017 | 0.312 |
LIG_SH2_NCK_1 | 827 | 831 | PF00017 | 0.474 |
LIG_SH2_SRC | 101 | 104 | PF00017 | 0.394 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.465 |
LIG_SH2_SRC | 44 | 47 | PF00017 | 0.454 |
LIG_SH2_SRC | 609 | 612 | PF00017 | 0.457 |
LIG_SH2_SRC | 678 | 681 | PF00017 | 0.447 |
LIG_SH2_SRC | 747 | 750 | PF00017 | 0.388 |
LIG_SH2_SRC | 799 | 802 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 747 | 751 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 799 | 803 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 640 | 643 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 831 | 834 | PF00017 | 0.394 |
LIG_SH3_2 | 492 | 497 | PF14604 | 0.565 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.778 |
LIG_SH3_5 | 674 | 678 | PF00018 | 0.303 |
LIG_SUMO_SIM_anti_2 | 237 | 244 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 408 | 413 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 410 | 415 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 503 | 509 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 611 | 618 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 767 | 775 | PF11976 | 0.340 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.394 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.529 |
LIG_TYR_ITIM | 829 | 834 | PF00017 | 0.472 |
MOD_CDC14_SPxK_1 | 494 | 497 | PF00782 | 0.563 |
MOD_CDK_SPxK_1 | 301 | 307 | PF00069 | 0.637 |
MOD_CDK_SPxK_1 | 491 | 497 | PF00069 | 0.565 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.297 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.495 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.305 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.661 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.588 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.724 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.718 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.556 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.489 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.491 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.304 |
MOD_CK1_1 | 764 | 770 | PF00069 | 0.238 |
MOD_CK1_1 | 812 | 818 | PF00069 | 0.567 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.513 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.330 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.297 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.310 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.363 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.639 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.548 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.461 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.585 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.412 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.547 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.396 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.334 |
MOD_CK2_1 | 789 | 795 | PF00069 | 0.312 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.383 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.490 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.352 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.704 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.527 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.641 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.558 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.703 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.476 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.422 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.306 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.433 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.241 |
MOD_GlcNHglycan | 813 | 817 | PF01048 | 0.467 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.503 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.436 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.368 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.476 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.370 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.450 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.633 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.471 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.379 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.548 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.527 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.603 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.688 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.522 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.318 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.419 |
MOD_LATS_1 | 129 | 135 | PF00433 | 0.299 |
MOD_N-GLC_2 | 93 | 95 | PF02516 | 0.405 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.343 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.462 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.391 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.495 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.515 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.588 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.562 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.413 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.547 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.506 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.310 |
MOD_NEK2_1 | 817 | 822 | PF00069 | 0.490 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.544 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.525 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.391 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.490 |
MOD_PK_1 | 131 | 137 | PF00069 | 0.319 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.437 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.360 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.582 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.493 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.482 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.231 |
MOD_PKA_2 | 778 | 784 | PF00069 | 0.231 |
MOD_PKB_1 | 476 | 484 | PF00069 | 0.530 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.384 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.429 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.249 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.745 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.644 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.642 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.752 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.575 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.280 |
MOD_SUMO_rev_2 | 169 | 179 | PF00179 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.307 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 754 | 757 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 831 | 834 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 475 | 478 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.459 |
TRG_NES_CRM1_1 | 410 | 423 | PF08389 | 0.452 |
TRG_NLS_MonoExtN_4 | 174 | 181 | PF00514 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 10 | 14 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 440 | 444 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P507 | Leptomonas seymouri | 47% | 100% |
A0A3Q8IDI5 | Leishmania donovani | 74% | 99% |
A4I1X3 | Leishmania infantum | 74% | 99% |
E9AY19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 99% |
Q4Q9F4 | Leishmania major | 73% | 100% |