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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005876 | spindle microtubule | 7 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0072686 | mitotic spindle | 6 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H7F1
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 7 |
GO:0007018 | microtubule-based movement | 3 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0000070 | mitotic sister chromatid segregation | 4 | 1 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0000819 | sister chromatid segregation | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0007059 | chromosome segregation | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0051225 | spindle assembly | 4 | 1 |
GO:0051231 | spindle elongation | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090307 | mitotic spindle assembly | 5 | 1 |
GO:0098813 | nuclear chromosome segregation | 3 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003774 | cytoskeletal motor activity | 1 | 7 |
GO:0003777 | microtubule motor activity | 2 | 7 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008017 | microtubule binding | 5 | 7 |
GO:0008092 | cytoskeletal protein binding | 3 | 7 |
GO:0015631 | tubulin binding | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 784 | 788 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 823 | 827 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 1021 | 1023 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 1055 | 1057 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 1061 | 1063 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 1021 | 1023 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 1034 | 1036 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 1055 | 1057 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 1061 | 1063 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 740 | 742 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 1034 | 1036 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 427 | 429 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 770 | 772 | PF00082 | 0.585 |
CLV_PCSK_PC7_1 | 766 | 772 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 843 | 847 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.653 |
DEG_APCC_DBOX_1 | 58 | 66 | PF00400 | 0.304 |
DEG_SIAH_1 | 611 | 619 | PF03145 | 0.641 |
DEG_SPOP_SBC_1 | 1040 | 1044 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 1050 | 1054 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 883 | 887 | PF00917 | 0.633 |
DOC_ANK_TNKS_1 | 110 | 117 | PF00023 | 0.303 |
DOC_CKS1_1 | 672 | 677 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 240 | 250 | PF00134 | 0.304 |
DOC_CYCLIN_RxL_1 | 402 | 412 | PF00134 | 0.386 |
DOC_CYCLIN_RxL_1 | 7 | 19 | PF00134 | 0.459 |
DOC_MAPK_gen_1 | 187 | 196 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 325 | 332 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 808 | 817 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.304 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.572 |
DOC_PP4_FxxP_1 | 518 | 521 | PF00568 | 0.608 |
DOC_USP7_MATH_1 | 1039 | 1043 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 1051 | 1055 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 883 | 887 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 954 | 958 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 996 | 1000 | PF00917 | 0.794 |
DOC_USP7_UBL2_3 | 448 | 452 | PF12436 | 0.584 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 851 | 856 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 908 | 913 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 926 | 931 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 958 | 963 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 153 | 160 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 187 | 197 | PF00244 | 0.224 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 387 | 396 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 532 | 536 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 595 | 602 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 604 | 612 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 713 | 722 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 741 | 747 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 781 | 790 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 810 | 817 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 843 | 850 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 871 | 877 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 997 | 1002 | PF00244 | 0.652 |
LIG_Actin_WH2_2 | 210 | 228 | PF00022 | 0.369 |
LIG_APCC_ABBA_1 | 126 | 131 | PF00400 | 0.304 |
LIG_APCC_ABBA_1 | 754 | 759 | PF00400 | 0.511 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.461 |
LIG_BIR_III_2 | 826 | 830 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_1 | 872 | 876 | PF00533 | 0.536 |
LIG_Clathr_ClatBox_1 | 214 | 218 | PF01394 | 0.304 |
LIG_EVH1_1 | 481 | 485 | PF00568 | 0.606 |
LIG_FHA_1 | 1007 | 1013 | PF00498 | 0.633 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.304 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.304 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.304 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.683 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.741 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.693 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.304 |
LIG_FHA_1 | 873 | 879 | PF00498 | 0.544 |
LIG_FHA_1 | 940 | 946 | PF00498 | 0.659 |
LIG_FHA_1 | 982 | 988 | PF00498 | 0.641 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.472 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.512 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.304 |
LIG_FHA_2 | 782 | 788 | PF00498 | 0.577 |
LIG_FHA_2 | 852 | 858 | PF00498 | 0.594 |
LIG_LIR_Apic_2 | 515 | 521 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 200 | 207 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 371 | 380 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 457 | 464 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 84 | 92 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.304 |
LIG_MYND_1 | 484 | 488 | PF01753 | 0.581 |
LIG_MYND_1 | 671 | 675 | PF01753 | 0.593 |
LIG_NRBOX | 273 | 279 | PF00104 | 0.304 |
LIG_NRBOX | 403 | 409 | PF00104 | 0.497 |
LIG_PCNA_PIPBox_1 | 208 | 217 | PF02747 | 0.304 |
LIG_PCNA_yPIPBox_3 | 737 | 750 | PF02747 | 0.526 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.549 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.493 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 731 | 734 | PF00017 | 0.689 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.304 |
LIG_SH3_1 | 533 | 539 | PF00018 | 0.561 |
LIG_SH3_3 | 1026 | 1032 | PF00018 | 0.645 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.635 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.569 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.649 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.557 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.579 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.649 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.573 |
LIG_SH3_3 | 933 | 939 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 142 | 149 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 706 | 712 | PF11976 | 0.600 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.575 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.620 |
LIG_TRAF2_1 | 49 | 52 | PF00917 | 0.369 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.637 |
LIG_UBA3_1 | 245 | 249 | PF00899 | 0.304 |
LIG_WRC_WIRS_1 | 932 | 937 | PF05994 | 0.558 |
MOD_CDC14_SPxK_1 | 529 | 532 | PF00782 | 0.632 |
MOD_CDC14_SPxK_1 | 617 | 620 | PF00782 | 0.620 |
MOD_CDC14_SPxK_1 | 961 | 964 | PF00782 | 0.634 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 614 | 620 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 958 | 964 | PF00069 | 0.641 |
MOD_CDK_SPxxK_3 | 526 | 533 | PF00069 | 0.676 |
MOD_CDK_SPxxK_3 | 614 | 621 | PF00069 | 0.624 |
MOD_CK1_1 | 1042 | 1048 | PF00069 | 0.654 |
MOD_CK1_1 | 1054 | 1060 | PF00069 | 0.690 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.304 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.407 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.304 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.304 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.369 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.624 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.560 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.613 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.641 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.643 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.692 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.735 |
MOD_CK1_1 | 904 | 910 | PF00069 | 0.491 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.304 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.466 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.575 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.369 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.575 |
MOD_Cter_Amidation | 1019 | 1022 | PF01082 | 0.684 |
MOD_GlcNHglycan | 1003 | 1006 | PF01048 | 0.644 |
MOD_GlcNHglycan | 1024 | 1027 | PF01048 | 0.809 |
MOD_GlcNHglycan | 1037 | 1040 | PF01048 | 0.639 |
MOD_GlcNHglycan | 1045 | 1048 | PF01048 | 0.649 |
MOD_GlcNHglycan | 1062 | 1065 | PF01048 | 0.543 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.304 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.304 |
MOD_GlcNHglycan | 514 | 518 | PF01048 | 0.661 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.701 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.628 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.704 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.535 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.605 |
MOD_GlcNHglycan | 704 | 708 | PF01048 | 0.688 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.503 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.507 |
MOD_GlcNHglycan | 886 | 889 | PF01048 | 0.624 |
MOD_GlcNHglycan | 906 | 909 | PF01048 | 0.471 |
MOD_GlcNHglycan | 973 | 976 | PF01048 | 0.721 |
MOD_GlcNHglycan | 987 | 990 | PF01048 | 0.594 |
MOD_GlcNHglycan | 994 | 997 | PF01048 | 0.604 |
MOD_GSK3_1 | 1001 | 1008 | PF00069 | 0.625 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.647 |
MOD_GSK3_1 | 1050 | 1057 | PF00069 | 0.632 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.304 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.304 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.183 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.304 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.304 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.304 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.302 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.734 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.588 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.639 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.671 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.713 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.622 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.531 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.325 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.532 |
MOD_GSK3_1 | 883 | 890 | PF00069 | 0.571 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.497 |
MOD_GSK3_1 | 954 | 961 | PF00069 | 0.620 |
MOD_GSK3_1 | 981 | 988 | PF00069 | 0.743 |
MOD_GSK3_1 | 992 | 999 | PF00069 | 0.536 |
MOD_LATS_1 | 1033 | 1039 | PF00433 | 0.690 |
MOD_N-GLC_1 | 1012 | 1017 | PF02516 | 0.564 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.310 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.694 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.304 |
MOD_N-GLC_1 | 742 | 747 | PF02516 | 0.495 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.441 |
MOD_NEK2_1 | 1001 | 1006 | PF00069 | 0.628 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.304 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.369 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.304 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.304 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.304 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.637 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.776 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.304 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.650 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.535 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.496 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.560 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.562 |
MOD_NEK2_1 | 985 | 990 | PF00069 | 0.690 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.304 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.304 |
MOD_NEK2_2 | 735 | 740 | PF00069 | 0.478 |
MOD_NEK2_2 | 981 | 986 | PF00069 | 0.528 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.304 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.503 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.425 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.304 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.536 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.745 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.689 |
MOD_PIKK_1 | 987 | 993 | PF00454 | 0.670 |
MOD_PK_1 | 313 | 319 | PF00069 | 0.304 |
MOD_PKA_1 | 1055 | 1061 | PF00069 | 0.664 |
MOD_PKA_2 | 1054 | 1060 | PF00069 | 0.632 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.278 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.304 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.363 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.256 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.297 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.314 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.498 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.683 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.618 |
MOD_PKA_2 | 603 | 609 | PF00069 | 0.631 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.715 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.653 |
MOD_PKA_2 | 809 | 815 | PF00069 | 0.568 |
MOD_PKA_2 | 870 | 876 | PF00069 | 0.530 |
MOD_PKA_2 | 969 | 975 | PF00069 | 0.765 |
MOD_PKA_2 | 981 | 987 | PF00069 | 0.601 |
MOD_PKA_2 | 996 | 1002 | PF00069 | 0.653 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.304 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.304 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.304 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.617 |
MOD_Plk_1 | 742 | 748 | PF00069 | 0.493 |
MOD_Plk_1 | 786 | 792 | PF00069 | 0.497 |
MOD_Plk_2-3 | 35 | 41 | PF00069 | 0.304 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.304 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.304 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.304 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.304 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.350 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.304 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.681 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.304 |
MOD_Plk_4 | 892 | 898 | PF00069 | 0.579 |
MOD_Plk_4 | 931 | 937 | PF00069 | 0.634 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.304 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.369 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.639 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.678 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.739 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.786 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.608 |
MOD_ProDKin_1 | 851 | 857 | PF00069 | 0.536 |
MOD_ProDKin_1 | 908 | 914 | PF00069 | 0.572 |
MOD_ProDKin_1 | 926 | 932 | PF00069 | 0.696 |
MOD_ProDKin_1 | 946 | 952 | PF00069 | 0.487 |
MOD_ProDKin_1 | 958 | 964 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 265 | 275 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 29 | 38 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 300 | 307 | PF00179 | 0.304 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.304 |
TRG_DiLeu_BaEn_1 | 324 | 329 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 705 | 710 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 638 | 640 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 739 | 741 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 814 | 817 | PF00400 | 0.594 |
TRG_NES_CRM1_1 | 326 | 338 | PF08389 | 0.495 |
TRG_NLS_Bipartite_1 | 1021 | 1038 | PF00514 | 0.633 |
TRG_NLS_MonoExtN_4 | 1031 | 1038 | PF00514 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 13 | 18 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBE0 | Leptomonas seymouri | 60% | 100% |
A4HE97 | Leishmania braziliensis | 80% | 100% |
A4I1P3 | Leishmania infantum | 99% | 100% |
E9AXS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q9P4 | Leishmania major | 94% | 99% |