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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0016592 | mediator complex | 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:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4I302
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0000086 | G2/M transition of mitotic cell cycle | 5 | 1 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 1 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044839 | cell cycle G2/M phase transition | 4 | 1 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 900 | 904 | PF00656 | 0.734 |
CLV_C14_Caspase3-7 | 932 | 936 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 799 | 801 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 921 | 923 | PF00675 | 0.735 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 921 | 923 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.574 |
CLV_Separin_Metazoa | 771 | 775 | PF03568 | 0.445 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.593 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.656 |
DEG_SPOP_SBC_1 | 396 | 400 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 819 | 823 | PF00917 | 0.622 |
DOC_CDC14_PxL_1 | 617 | 625 | PF14671 | 0.291 |
DOC_CYCLIN_RxL_1 | 647 | 657 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 648 | 654 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 577 | 586 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 348 | 356 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 489 | 497 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 94 | 101 | PF00069 | 0.516 |
DOC_MAPK_RevD_3 | 634 | 650 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 562 | 569 | PF00149 | 0.385 |
DOC_PP2B_LxvP_1 | 669 | 672 | PF13499 | 0.367 |
DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 788 | 792 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 864 | 868 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 874 | 878 | PF00917 | 0.700 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.421 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 860 | 865 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 866 | 871 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 233 | 240 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 275 | 283 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 509 | 518 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 695 | 705 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 825 | 833 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 921 | 928 | PF00244 | 0.610 |
LIG_BIR_III_4 | 149 | 153 | PF00653 | 0.582 |
LIG_Clathr_ClatBox_1 | 367 | 371 | PF01394 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 635 | 643 | PF00928 | 0.367 |
LIG_EVH1_2 | 75 | 79 | PF00568 | 0.664 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.761 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.728 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.536 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.684 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.408 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.692 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.303 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.291 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.367 |
LIG_FHA_1 | 936 | 942 | PF00498 | 0.585 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.648 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.452 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.620 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.750 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.569 |
LIG_LIR_Apic_2 | 615 | 621 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 492 | 502 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 557 | 568 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 588 | 599 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 588 | 594 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 674 | 680 | PF02991 | 0.315 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.522 |
LIG_Pex14_2 | 643 | 647 | PF04695 | 0.367 |
LIG_REV1ctd_RIR_1 | 757 | 763 | PF16727 | 0.319 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.407 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.328 |
LIG_SH2_CRK | 560 | 564 | PF00017 | 0.367 |
LIG_SH2_CRK | 681 | 685 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 270 | 274 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 511 | 515 | PF00017 | 0.506 |
LIG_SH2_PTP2 | 591 | 594 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 630 | 634 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 293 | 296 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.357 |
LIG_SH3_2 | 202 | 207 | PF14604 | 0.619 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.600 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.736 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.465 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.669 |
LIG_SH3_3 | 763 | 769 | PF00018 | 0.445 |
LIG_SH3_CIN85_PxpxPR_1 | 372 | 377 | PF14604 | 0.673 |
LIG_SUMO_SIM_anti_2 | 349 | 354 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 366 | 371 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 612 | 618 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 731 | 739 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 366 | 371 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 661 | 667 | PF11976 | 0.385 |
LIG_TRAF2_1 | 672 | 675 | PF00917 | 0.363 |
LIG_TYR_ITIM | 533 | 538 | PF00017 | 0.521 |
LIG_TYR_ITIM | 558 | 563 | PF00017 | 0.367 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.554 |
MOD_CDC14_SPxK_1 | 381 | 384 | PF00782 | 0.631 |
MOD_CDK_SPK_2 | 536 | 541 | PF00069 | 0.545 |
MOD_CDK_SPxK_1 | 378 | 384 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 370 | 377 | PF00069 | 0.646 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.665 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.792 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.656 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.577 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.698 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.769 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.596 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.513 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.610 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.385 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.659 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.513 |
MOD_CK1_1 | 813 | 819 | PF00069 | 0.658 |
MOD_CK1_1 | 827 | 833 | PF00069 | 0.595 |
MOD_CK1_1 | 853 | 859 | PF00069 | 0.635 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.513 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.713 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.567 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.685 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.654 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.582 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.557 |
MOD_CK2_1 | 747 | 753 | PF00069 | 0.325 |
MOD_CK2_1 | 840 | 846 | PF00069 | 0.631 |
MOD_CK2_1 | 851 | 857 | PF00069 | 0.622 |
MOD_CK2_1 | 931 | 937 | PF00069 | 0.612 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.728 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.801 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.675 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.612 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.657 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.400 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.651 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.661 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.711 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.659 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.340 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.206 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.797 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.729 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.675 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.737 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.774 |
MOD_GlcNHglycan | 866 | 869 | PF01048 | 0.649 |
MOD_GlcNHglycan | 898 | 902 | PF01048 | 0.691 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.504 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.615 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.638 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.526 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.675 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.631 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.679 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.661 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.665 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.704 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.575 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.681 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.710 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.680 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.338 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.408 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.782 |
MOD_GSK3_1 | 853 | 860 | PF00069 | 0.685 |
MOD_GSK3_1 | 876 | 883 | PF00069 | 0.736 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.617 |
MOD_GSK3_1 | 917 | 924 | PF00069 | 0.683 |
MOD_GSK3_1 | 931 | 938 | PF00069 | 0.716 |
MOD_LATS_1 | 919 | 925 | PF00433 | 0.690 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.665 |
MOD_N-GLC_1 | 696 | 701 | PF02516 | 0.454 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.529 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.412 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.281 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.319 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.367 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.650 |
MOD_NEK2_2 | 876 | 881 | PF00069 | 0.549 |
MOD_OFUCOSY | 98 | 103 | PF10250 | 0.548 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.647 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.494 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.517 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.687 |
MOD_PIKK_1 | 805 | 811 | PF00454 | 0.691 |
MOD_PK_1 | 554 | 560 | PF00069 | 0.385 |
MOD_PKA_1 | 747 | 753 | PF00069 | 0.385 |
MOD_PKA_1 | 921 | 927 | PF00069 | 0.695 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.649 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.628 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.476 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.766 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.599 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.385 |
MOD_PKA_2 | 747 | 753 | PF00069 | 0.291 |
MOD_PKA_2 | 805 | 811 | PF00069 | 0.642 |
MOD_PKA_2 | 824 | 830 | PF00069 | 0.492 |
MOD_PKA_2 | 920 | 926 | PF00069 | 0.713 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.596 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.576 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.291 |
MOD_Plk_1 | 845 | 851 | PF00069 | 0.627 |
MOD_Plk_2-3 | 931 | 937 | PF00069 | 0.612 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.483 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.567 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.565 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.388 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.566 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.405 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.300 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.598 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.328 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.341 |
MOD_Plk_4 | 736 | 742 | PF00069 | 0.447 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.637 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.709 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.539 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.604 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.537 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.385 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.576 |
MOD_ProDKin_1 | 860 | 866 | PF00069 | 0.663 |
MOD_SUMO_for_1 | 760 | 763 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 520 | 527 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 572 | 582 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_4 | 911 | 917 | PF01217 | 0.633 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.385 |
TRG_NLS_Bipartite_1 | 424 | 444 | PF00514 | 0.599 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.551 |
TRG_NLS_MonoExtC_3 | 439 | 445 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 573 | 578 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 946 | 951 | PF00026 | 0.737 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6G8 | Leptomonas seymouri | 49% | 100% |
A0A3R7KFZ3 | Trypanosoma rangeli | 38% | 100% |
A0A3S5H7I2 | Leishmania donovani | 99% | 100% |
A4HFW9 | Leishmania braziliensis | 77% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ADH4 | Leishmania major | 92% | 100% |
E9AZ98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |