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 | yes | yes: 1, no: 14 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 16 |
GO:0042995 | cell projection | 2 | 16 |
GO:0043226 | organelle | 2 | 16 |
GO:0043227 | membrane-bounded organelle | 3 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 16 |
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:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: E9ACE9
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 | 2 |
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:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006952 | defense response | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
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:0005488 | binding | 1 | 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 | 104 | 108 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 824 | 828 | PF00656 | 0.336 |
CLV_C14_Caspase3-7 | 897 | 901 | PF00656 | 0.250 |
CLV_C14_Caspase3-7 | 913 | 917 | PF00656 | 0.321 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 864 | 866 | PF00675 | 0.425 |
CLV_PCSK_FUR_1 | 491 | 495 | PF00082 | 0.263 |
CLV_PCSK_FUR_1 | 812 | 816 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 814 | 816 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 876 | 880 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 998 | 1002 | PF00082 | 0.403 |
DEG_ODPH_VHL_1 | 620 | 631 | PF01847 | 0.276 |
DEG_SCF_SKP2-CKS1_1 | 410 | 417 | PF00560 | 0.245 |
DOC_CDC14_PxL_1 | 228 | 236 | PF14671 | 0.414 |
DOC_CYCLIN_RxL_1 | 192 | 201 | PF00134 | 0.557 |
DOC_MAPK_DCC_7 | 409 | 418 | PF00069 | 0.253 |
DOC_MAPK_DCC_7 | 616 | 625 | PF00069 | 0.327 |
DOC_MAPK_DCC_7 | 646 | 654 | PF00069 | 0.241 |
DOC_MAPK_gen_1 | 192 | 199 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 352 | 359 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 409 | 418 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 719 | 726 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 865 | 874 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 417 | 425 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 570 | 578 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 646 | 654 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 738 | 746 | PF00069 | 0.275 |
DOC_PP1_RVXF_1 | 194 | 200 | PF00149 | 0.318 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.247 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.280 |
DOC_PP4_FxxP_1 | 647 | 650 | PF00568 | 0.252 |
DOC_SPAK_OSR1_1 | 141 | 145 | PF12202 | 0.347 |
DOC_SPAK_OSR1_1 | 646 | 650 | PF12202 | 0.340 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 753 | 757 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 782 | 786 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 831 | 835 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 898 | 902 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 923 | 927 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 944 | 948 | PF00917 | 0.340 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 384 | 391 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 509 | 517 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 541 | 550 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 554 | 558 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 616 | 624 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 646 | 650 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 662 | 670 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 679 | 688 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 73 | 77 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 738 | 742 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 950 | 956 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 960 | 965 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 102 | 120 | PF00022 | 0.477 |
LIG_Actin_WH2_2 | 433 | 449 | PF00022 | 0.375 |
LIG_Actin_WH2_2 | 571 | 586 | PF00022 | 0.387 |
LIG_Actin_WH2_2 | 663 | 678 | PF00022 | 0.466 |
LIG_Actin_WH2_2 | 754 | 770 | PF00022 | 0.298 |
LIG_Actin_WH2_2 | 800 | 816 | PF00022 | 0.334 |
LIG_Actin_WH2_2 | 860 | 878 | PF00022 | 0.547 |
LIG_Actin_WH2_2 | 892 | 908 | PF00022 | 0.464 |
LIG_Actin_WH2_2 | 970 | 988 | PF00022 | 0.326 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.434 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 834 | 838 | PF00533 | 0.294 |
LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.217 |
LIG_DLG_GKlike_1 | 868 | 875 | PF00625 | 0.325 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.530 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.455 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.465 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.377 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.391 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.459 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.441 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.537 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.354 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.333 |
LIG_FHA_1 | 986 | 992 | PF00498 | 0.411 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.549 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.577 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.452 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.306 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.379 |
LIG_FHA_2 | 789 | 795 | PF00498 | 0.463 |
LIG_FHA_2 | 822 | 828 | PF00498 | 0.556 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.345 |
LIG_FHA_2 | 911 | 917 | PF00498 | 0.459 |
LIG_FHA_2 | 938 | 944 | PF00498 | 0.522 |
LIG_GBD_Chelix_1 | 101 | 109 | PF00786 | 0.276 |
LIG_LIR_Apic_2 | 204 | 208 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 699 | 704 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 835 | 846 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 699 | 703 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 835 | 841 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 849 | 853 | PF02991 | 0.326 |
LIG_MYND_3 | 649 | 653 | PF01753 | 0.344 |
LIG_NRBOX | 468 | 474 | PF00104 | 0.260 |
LIG_SH2_PTP2 | 69 | 72 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 725 | 728 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 771 | 774 | PF00017 | 0.407 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.355 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.336 |
LIG_SUMO_SIM_anti_2 | 286 | 292 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.307 |
LIG_SUMO_SIM_anti_2 | 514 | 519 | PF11976 | 0.272 |
LIG_SUMO_SIM_anti_2 | 573 | 578 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 651 | 656 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 699 | 705 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 743 | 748 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 789 | 794 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 926 | 932 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 621 | 627 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 791 | 796 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 975 | 980 | PF11976 | 0.311 |
MOD_CDC14_SPxK_1 | 529 | 532 | PF00782 | 0.443 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.264 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.449 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.436 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.518 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.512 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.644 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.367 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.569 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.347 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.437 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.414 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.432 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.387 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.468 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.509 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.413 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.508 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.354 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.406 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.349 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.365 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.472 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.277 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.296 |
MOD_CK1_1 | 858 | 864 | PF00069 | 0.460 |
MOD_CK1_1 | 914 | 920 | PF00069 | 0.471 |
MOD_CK1_1 | 926 | 932 | PF00069 | 0.381 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.544 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.303 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.539 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.532 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.447 |
MOD_CK2_1 | 788 | 794 | PF00069 | 0.375 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.359 |
MOD_CK2_1 | 937 | 943 | PF00069 | 0.478 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.334 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.532 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.441 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.335 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.436 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.661 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.400 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.415 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.439 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.427 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.374 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.437 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.539 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.409 |
MOD_GlcNHglycan | 757 | 761 | PF01048 | 0.233 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.460 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.416 |
MOD_GlcNHglycan | 886 | 890 | PF01048 | 0.469 |
MOD_GlcNHglycan | 895 | 899 | PF01048 | 0.523 |
MOD_GlcNHglycan | 900 | 903 | PF01048 | 0.265 |
MOD_GlcNHglycan | 923 | 926 | PF01048 | 0.435 |
MOD_GlcNHglycan | 946 | 949 | PF01048 | 0.560 |
MOD_GlcNHglycan | 969 | 972 | PF01048 | 0.574 |
MOD_GlcNHglycan | 978 | 982 | PF01048 | 0.456 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.671 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.464 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.378 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.543 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.516 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.383 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.576 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.370 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.410 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.466 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.474 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.326 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.400 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.467 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.532 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.487 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.409 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.314 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.324 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.372 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.377 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.247 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.409 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.416 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.469 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.303 |
MOD_GSK3_1 | 956 | 963 | PF00069 | 0.453 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.474 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.409 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.353 |
MOD_N-GLC_1 | 819 | 824 | PF02516 | 0.309 |
MOD_N-GLC_1 | 839 | 844 | PF02516 | 0.187 |
MOD_N-GLC_1 | 911 | 916 | PF02516 | 0.296 |
MOD_N-GLC_1 | 937 | 942 | PF02516 | 0.528 |
MOD_N-GLC_2 | 64 | 66 | PF02516 | 0.510 |
MOD_N-GLC_2 | 934 | 936 | PF02516 | 0.264 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.612 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.619 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.439 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.351 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.431 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.361 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.346 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.347 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.416 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.370 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.399 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.374 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.376 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.285 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.443 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.349 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.464 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.444 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.571 |
MOD_NEK2_1 | 726 | 731 | PF00069 | 0.336 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.283 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.370 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.415 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.287 |
MOD_NEK2_1 | 818 | 823 | PF00069 | 0.368 |
MOD_NEK2_1 | 910 | 915 | PF00069 | 0.408 |
MOD_NEK2_1 | 921 | 926 | PF00069 | 0.446 |
MOD_NEK2_1 | 956 | 961 | PF00069 | 0.412 |
MOD_NEK2_1 | 967 | 972 | PF00069 | 0.424 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.540 |
MOD_NEK2_1 | 985 | 990 | PF00069 | 0.529 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.304 |
MOD_NEK2_2 | 855 | 860 | PF00069 | 0.332 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.454 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.476 |
MOD_PIKK_1 | 578 | 584 | PF00454 | 0.331 |
MOD_PK_1 | 116 | 122 | PF00069 | 0.386 |
MOD_PK_1 | 314 | 320 | PF00069 | 0.340 |
MOD_PK_1 | 776 | 782 | PF00069 | 0.304 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.292 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.322 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.343 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.564 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.310 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.332 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.418 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.533 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.516 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.486 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.481 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.320 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.444 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.367 |
MOD_PKA_2 | 737 | 743 | PF00069 | 0.453 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.274 |
MOD_PKA_2 | 949 | 955 | PF00069 | 0.502 |
MOD_PKA_2 | 959 | 965 | PF00069 | 0.408 |
MOD_PKA_2 | 985 | 991 | PF00069 | 0.592 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.515 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.459 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.439 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.408 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.459 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.334 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.474 |
MOD_Plk_1 | 819 | 825 | PF00069 | 0.503 |
MOD_Plk_1 | 894 | 900 | PF00069 | 0.331 |
MOD_Plk_1 | 911 | 917 | PF00069 | 0.250 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.537 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.317 |
MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.348 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.410 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.521 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.349 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.464 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.344 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.463 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.515 |
MOD_Plk_4 | 788 | 794 | PF00069 | 0.423 |
MOD_Plk_4 | 858 | 864 | PF00069 | 0.476 |
MOD_Plk_4 | 926 | 932 | PF00069 | 0.466 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.457 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.431 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.481 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.301 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.429 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.430 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.380 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.449 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.548 |
TRG_DiLeu_BaEn_1 | 665 | 670 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 699 | 704 | PF01217 | 0.233 |
TRG_DiLeu_BaLyEn_6 | 619 | 624 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 811 | 814 | PF00400 | 0.353 |
TRG_NLS_MonoExtC_3 | 864 | 870 | PF00514 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 218 | 223 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 719 | 723 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 865 | 870 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 998 | 1003 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8B3 | Leptomonas seymouri | 30% | 68% |
A0A0N1P921 | Leptomonas seymouri | 28% | 100% |
A0A0S4J2Y5 | Bodo saltans | 22% | 100% |
A0A3S5ISR4 | Trypanosoma rangeli | 24% | 100% |
A0A451EJK8 | Leishmania donovani | 88% | 94% |
A4H3H4 | Leishmania braziliensis | 71% | 100% |
A4H3R1 | Leishmania braziliensis | 26% | 100% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A5U4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 72% |
E9AEF0 | Leishmania major | 26% | 100% |
E9AG21 | Leishmania infantum | 88% | 99% |
E9AJN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QD45 | Leishmania major | 27% | 100% |
V5BKI3 | Trypanosoma cruzi | 25% | 100% |