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: 1, no: 15 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 17 |
GO:0042995 | cell projection | 2 | 17 |
GO:0043226 | organelle | 2 | 17 |
GO:0043227 | membrane-bounded organelle | 3 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 17 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: A4H3H4
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:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 3 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
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:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 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:0006950 | response to stress | 2 | 2 |
GO:0006952 | defense response | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007021 | tubulin complex assembly | 6 | 1 |
GO:0007023 | post-chaperonin tubulin folding pathway | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.291 |
CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.223 |
CLV_C14_Caspase3-7 | 611 | 615 | PF00656 | 0.203 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 798 | 802 | PF00656 | 0.284 |
CLV_C14_Caspase3-7 | 887 | 891 | PF00656 | 0.254 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.447 |
CLV_PCSK_FUR_1 | 786 | 790 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 850 | 854 | PF00082 | 0.527 |
CLV_Separin_Metazoa | 939 | 943 | PF03568 | 0.262 |
DEG_ODPH_VHL_1 | 341 | 353 | PF01847 | 0.205 |
DEG_ODPH_VHL_1 | 594 | 605 | PF01847 | 0.246 |
DOC_CDC14_PxL_1 | 173 | 181 | PF14671 | 0.266 |
DOC_CDC14_PxL_1 | 202 | 210 | PF14671 | 0.532 |
DOC_CDC14_PxL_1 | 224 | 232 | PF14671 | 0.214 |
DOC_CDC14_PxL_1 | 804 | 812 | PF14671 | 0.198 |
DOC_CYCLIN_RxL_1 | 693 | 703 | PF00134 | 0.273 |
DOC_MAPK_DCC_7 | 590 | 599 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 544 | 552 | PF00069 | 0.317 |
DOC_PP1_RVXF_1 | 168 | 174 | PF00149 | 0.275 |
DOC_PP1_RVXF_1 | 648 | 655 | PF00149 | 0.361 |
DOC_SPAK_OSR1_1 | 620 | 624 | PF12202 | 0.305 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.216 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.231 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.220 |
DOC_USP7_MATH_1 | 727 | 731 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 842 | 846 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 872 | 876 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 918 | 922 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.250 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.205 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 404 | 409 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 416 | 423 | PF00244 | 0.228 |
LIG_14-3-3_CanoR_1 | 437 | 447 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 515 | 524 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 528 | 538 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 590 | 597 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 598 | 604 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 620 | 629 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 636 | 644 | PF00244 | 0.226 |
LIG_14-3-3_CanoR_1 | 653 | 662 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 666 | 672 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 682 | 689 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 712 | 720 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 896 | 905 | PF00244 | 0.204 |
LIG_14-3-3_CanoR_1 | 934 | 940 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 942 | 950 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 405 | 423 | PF00022 | 0.268 |
LIG_Actin_WH2_2 | 545 | 560 | PF00022 | 0.332 |
LIG_Actin_WH2_2 | 637 | 652 | PF00022 | 0.415 |
LIG_Actin_WH2_2 | 774 | 790 | PF00022 | 0.282 |
LIG_Actin_WH2_2 | 81 | 97 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 834 | 852 | PF00022 | 0.294 |
LIG_Actin_WH2_2 | 866 | 882 | PF00022 | 0.281 |
LIG_Actin_WH2_2 | 912 | 928 | PF00022 | 0.270 |
LIG_APCC_ABBA_1 | 806 | 811 | PF00400 | 0.192 |
LIG_Clathr_ClatBox_1 | 764 | 768 | PF01394 | 0.218 |
LIG_deltaCOP1_diTrp_1 | 62 | 71 | PF00928 | 0.339 |
LIG_EH1_1 | 405 | 413 | PF00400 | 0.274 |
LIG_EH1_1 | 758 | 766 | PF00400 | 0.199 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.580 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.310 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.392 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.394 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.237 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.368 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.264 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.354 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.346 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.405 |
LIG_FHA_1 | 851 | 857 | PF00498 | 0.522 |
LIG_FHA_1 | 936 | 942 | PF00498 | 0.294 |
LIG_FHA_1 | 961 | 967 | PF00498 | 0.613 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.340 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.444 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.358 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.460 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.244 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.257 |
LIG_FHA_2 | 885 | 891 | PF00498 | 0.402 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 811 | 820 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 811 | 815 | PF02991 | 0.421 |
LIG_PCNA_yPIPBox_3 | 758 | 771 | PF02747 | 0.196 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.599 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 699 | 702 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.442 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.408 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.265 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.332 |
LIG_SH3_3 | 802 | 808 | PF00018 | 0.207 |
LIG_SH3_3 | 845 | 851 | PF00018 | 0.303 |
LIG_SUMO_SIM_anti_2 | 350 | 355 | PF11976 | 0.258 |
LIG_SUMO_SIM_anti_2 | 440 | 447 | PF11976 | 0.254 |
LIG_SUMO_SIM_anti_2 | 546 | 552 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 579 | 584 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 624 | 630 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 717 | 722 | PF11976 | 0.244 |
LIG_SUMO_SIM_anti_2 | 776 | 782 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 844 | 850 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 900 | 906 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.208 |
LIG_SUMO_SIM_par_1 | 453 | 458 | PF11976 | 0.211 |
LIG_SUMO_SIM_par_1 | 624 | 630 | PF11976 | 0.191 |
LIG_SUMO_SIM_par_1 | 949 | 954 | PF11976 | 0.281 |
LIG_TRAF2_1 | 855 | 858 | PF00917 | 0.205 |
LIG_TYR_ITIM | 253 | 258 | PF00017 | 0.291 |
LIG_UBA3_1 | 390 | 398 | PF00899 | 0.215 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.403 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.339 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.382 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.329 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.439 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.454 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.385 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.250 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.491 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.441 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.322 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.706 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.302 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.223 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.429 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.437 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.314 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.449 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.365 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.253 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.313 |
MOD_CK1_1 | 832 | 838 | PF00069 | 0.387 |
MOD_CK1_1 | 900 | 906 | PF00069 | 0.510 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.357 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.205 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.201 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.441 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.287 |
MOD_CK2_1 | 852 | 858 | PF00069 | 0.331 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.476 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.514 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.483 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.301 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.342 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.400 |
MOD_GlcNHglycan | 639 | 643 | PF01048 | 0.251 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.468 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.486 |
MOD_GlcNHglycan | 774 | 778 | PF01048 | 0.424 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.489 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.451 |
MOD_GlcNHglycan | 860 | 864 | PF01048 | 0.458 |
MOD_GlcNHglycan | 869 | 873 | PF01048 | 0.456 |
MOD_GlcNHglycan | 874 | 877 | PF01048 | 0.392 |
MOD_GlcNHglycan | 897 | 900 | PF01048 | 0.394 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.411 |
MOD_GlcNHglycan | 943 | 946 | PF01048 | 0.456 |
MOD_GlcNHglycan | 952 | 956 | PF01048 | 0.411 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.475 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.427 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.422 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.481 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.391 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.316 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.377 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.350 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.449 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.354 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.469 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.346 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.268 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.402 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.457 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.308 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.358 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.401 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.378 |
MOD_GSK3_1 | 930 | 937 | PF00069 | 0.412 |
MOD_LATS_1 | 427 | 433 | PF00433 | 0.221 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.370 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.307 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.307 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.254 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.365 |
MOD_N-GLC_1 | 793 | 798 | PF02516 | 0.400 |
MOD_N-GLC_1 | 813 | 818 | PF02516 | 0.300 |
MOD_N-GLC_1 | 911 | 916 | PF02516 | 0.519 |
MOD_N-GLC_1 | 935 | 940 | PF02516 | 0.346 |
MOD_N-GLC_1 | 960 | 965 | PF02516 | 0.350 |
MOD_N-GLC_1 | 966 | 971 | PF02516 | 0.390 |
MOD_N-GLC_2 | 25 | 27 | PF02516 | 0.395 |
MOD_N-GLC_2 | 41 | 43 | PF02516 | 0.350 |
MOD_N-GLC_2 | 886 | 888 | PF02516 | 0.225 |
MOD_N-GLC_2 | 908 | 910 | PF02516 | 0.228 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.504 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.341 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.306 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.360 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.340 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.316 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.366 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.483 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.607 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.447 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.505 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.417 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.358 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.332 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.467 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.415 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.457 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.470 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.418 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.304 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.317 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.554 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.327 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.327 |
MOD_NEK2_1 | 757 | 762 | PF00069 | 0.395 |
MOD_NEK2_1 | 767 | 772 | PF00069 | 0.366 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.315 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.408 |
MOD_NEK2_1 | 895 | 900 | PF00069 | 0.426 |
MOD_NEK2_1 | 930 | 935 | PF00069 | 0.382 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.361 |
MOD_NEK2_1 | 959 | 964 | PF00069 | 0.317 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.197 |
MOD_NEK2_2 | 829 | 834 | PF00069 | 0.443 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.273 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.368 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.229 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.382 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.246 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.412 |
MOD_PK_1 | 404 | 410 | PF00069 | 0.214 |
MOD_PK_1 | 429 | 435 | PF00069 | 0.222 |
MOD_PK_1 | 671 | 677 | PF00069 | 0.222 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.294 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.359 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.232 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.407 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.318 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.415 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.523 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.425 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.542 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.408 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.329 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.490 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.511 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.479 |
MOD_PKA_2 | 895 | 901 | PF00069 | 0.211 |
MOD_PKA_2 | 930 | 936 | PF00069 | 0.404 |
MOD_PKA_2 | 941 | 947 | PF00069 | 0.332 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.434 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.345 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.390 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.202 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.423 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.295 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.318 |
MOD_Plk_1 | 868 | 874 | PF00069 | 0.385 |
MOD_Plk_1 | 880 | 886 | PF00069 | 0.325 |
MOD_Plk_1 | 911 | 917 | PF00069 | 0.290 |
MOD_Plk_1 | 960 | 966 | PF00069 | 0.496 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.256 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.342 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.276 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.379 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.634 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.377 |
MOD_Plk_4 | 816 | 822 | PF00069 | 0.285 |
MOD_Plk_4 | 832 | 838 | PF00069 | 0.398 |
MOD_Plk_4 | 900 | 906 | PF00069 | 0.254 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.294 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.287 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.254 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.523 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.304 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.209 |
MOD_SUMO_rev_2 | 139 | 146 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.211 |
TRG_DiLeu_BaEn_1 | 639 | 644 | PF01217 | 0.290 |
TRG_DiLeu_BaEn_2 | 124 | 130 | PF01217 | 0.246 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.220 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 785 | 788 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 928 | 931 | PF00400 | 0.297 |
TRG_NES_CRM1_1 | 363 | 376 | PF08389 | 0.291 |
TRG_NES_CRM1_1 | 617 | 630 | PF08389 | 0.204 |
TRG_NES_CRM1_1 | 755 | 768 | PF08389 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 839 | 844 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P921 | Leptomonas seymouri | 27% | 100% |
A0A0S4J2Y5 | Bodo saltans | 23% | 100% |
A0A1X0P1M5 | Trypanosomatidae | 23% | 100% |
A0A3S5ISR4 | Trypanosoma rangeli | 25% | 100% |
A0A451EJK8 | Leishmania donovani | 71% | 91% |
A4H3R1 | Leishmania braziliensis | 27% | 100% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A5U4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 70% |
E9ACE9 | Leishmania major | 71% | 100% |
E9AEF0 | Leishmania major | 24% | 100% |
E9AG21 | Leishmania infantum | 71% | 97% |
E9AJN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
O23530 | Arabidopsis thaliana | 21% | 68% |
Q4Q0S9 | Leishmania major | 24% | 81% |
Q4Q6A2 | Leishmania major | 22% | 100% |
Q4QD45 | Leishmania major | 29% | 100% |