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:0005811 | lipid droplet | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IE08
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0034389 | lipid droplet organization | 5 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0055088 | lipid homeostasis | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004645 | 1,4-alpha-oligoglucan phosphorylase activity | 5 | 3 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016757 | glycosyltransferase activity | 3 | 5 |
GO:0016758 | hexosyltransferase activity | 4 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
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:0102250 | linear malto-oligosaccharide phosphorylase activity | 5 | 3 |
GO:0102499 | SHG alpha-glucan phosphorylase activity | 5 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.736 |
CLV_C14_Caspase3-7 | 617 | 621 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.523 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 738 | 740 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 556 | 562 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 208 | 212 | PF03568 | 0.496 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.481 |
DEG_SCF_FBW7_1 | 15 | 21 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 115 | 119 | PF00917 | 0.474 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.553 |
DOC_CKS1_1 | 579 | 584 | PF01111 | 0.673 |
DOC_CYCLIN_RxL_1 | 139 | 152 | PF00134 | 0.492 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.530 |
DOC_CYCLIN_RxL_1 | 553 | 562 | PF00134 | 0.342 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 396 | 407 | PF00069 | 0.728 |
DOC_MAPK_gen_1 | 525 | 534 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 570 | 578 | PF00069 | 0.614 |
DOC_MAPK_RevD_3 | 546 | 561 | PF00069 | 0.313 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.612 |
DOC_PP2B_LxvP_1 | 730 | 733 | PF13499 | 0.771 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.847 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.819 |
DOC_USP7_MATH_1 | 733 | 737 | PF00917 | 0.840 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.492 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.845 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 845 | 850 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 396 | 404 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 525 | 531 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 684 | 690 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 706 | 711 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 774 | 782 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 802 | 811 | PF00244 | 0.702 |
LIG_APCC_ABBAyCdc20_2 | 157 | 163 | PF00400 | 0.576 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.832 |
LIG_eIF4E_1 | 142 | 148 | PF01652 | 0.574 |
LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.492 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.725 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.492 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.587 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.537 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.450 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.492 |
LIG_FHA_1 | 741 | 747 | PF00498 | 0.715 |
LIG_FHA_1 | 793 | 799 | PF00498 | 0.764 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.749 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 551 | 559 | PF00786 | 0.453 |
LIG_Integrin_RGD_1 | 244 | 246 | PF01839 | 0.376 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 577 | 583 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.779 |
LIG_LIR_Gen_1 | 458 | 465 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 484 | 495 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 574 | 583 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.807 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 865 | 870 | PF02991 | 0.714 |
LIG_NBox_RRM_1 | 403 | 413 | PF00076 | 0.682 |
LIG_NRBOX | 554 | 560 | PF00104 | 0.342 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.576 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.492 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.555 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.571 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.775 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.715 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 721 | 725 | PF00017 | 0.743 |
LIG_SH2_STAT3 | 143 | 146 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.781 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.492 |
LIG_SH3_1 | 580 | 586 | PF00018 | 0.640 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.592 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.735 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.713 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.660 |
LIG_SH3_3 | 687 | 693 | PF00018 | 0.799 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.754 |
LIG_SH3_3 | 846 | 852 | PF00018 | 0.706 |
LIG_SH3_CIN85_PxpxPR_1 | 673 | 678 | PF14604 | 0.748 |
LIG_SUMO_SIM_anti_2 | 98 | 105 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 248 | 258 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.783 |
LIG_SxIP_EBH_1 | 625 | 638 | PF03271 | 0.665 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.665 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.778 |
LIG_WRC_WIRS_1 | 465 | 470 | PF05994 | 0.673 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.645 |
LIG_WW_3 | 581 | 585 | PF00397 | 0.642 |
MOD_CDK_SPxK_1 | 578 | 584 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 806 | 812 | PF00069 | 0.747 |
MOD_CDK_SPxxK_3 | 578 | 585 | PF00069 | 0.753 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.471 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.697 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.513 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.755 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.719 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.741 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.687 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.689 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.776 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.647 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.680 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.648 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.828 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.765 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.623 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.821 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.693 |
MOD_CK1_1 | 792 | 798 | PF00069 | 0.696 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.792 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.721 |
MOD_CK1_1 | 837 | 843 | PF00069 | 0.742 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.686 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.704 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.675 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.741 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.689 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.730 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.702 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.652 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.768 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.292 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.334 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.330 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.376 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.552 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.493 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.447 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.298 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.516 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.509 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.512 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.555 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.498 |
MOD_GlcNHglycan | 620 | 624 | PF01048 | 0.612 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.430 |
MOD_GlcNHglycan | 726 | 730 | PF01048 | 0.571 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.503 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.524 |
MOD_GlcNHglycan | 835 | 839 | PF01048 | 0.513 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.599 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.549 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.585 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.416 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.668 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.755 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.750 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.723 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.767 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.672 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.780 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.651 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.659 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.721 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.704 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.673 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.661 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.681 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.843 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.492 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.746 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.694 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.666 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.685 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.769 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.779 |
MOD_LATS_1 | 680 | 686 | PF00433 | 0.762 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.584 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.536 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.486 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.583 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.492 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.691 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.704 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.718 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.672 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.683 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.476 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.802 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.678 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.710 |
MOD_NEK2_1 | 834 | 839 | PF00069 | 0.744 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.492 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.492 |
MOD_NEK2_2 | 797 | 802 | PF00069 | 0.769 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.796 |
MOD_PIKK_1 | 698 | 704 | PF00454 | 0.833 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.723 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.764 |
MOD_PKA_1 | 706 | 712 | PF00069 | 0.764 |
MOD_PKA_1 | 774 | 780 | PF00069 | 0.708 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.476 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.576 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.492 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.764 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.697 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.762 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.396 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.665 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.764 |
MOD_PKA_2 | 773 | 779 | PF00069 | 0.729 |
MOD_PKB_1 | 761 | 769 | PF00069 | 0.813 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.576 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.771 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.708 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.697 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.769 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.781 |
MOD_Plk_1 | 725 | 731 | PF00069 | 0.730 |
MOD_Plk_1 | 766 | 772 | PF00069 | 0.815 |
MOD_Plk_1 | 834 | 840 | PF00069 | 0.678 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.576 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.703 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.492 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.542 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.494 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.495 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.660 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.635 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.684 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.721 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.680 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.504 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.553 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.484 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.708 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.778 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.795 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.663 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.675 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.754 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.499 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.846 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.766 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.770 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.706 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.754 |
MOD_ProDKin_1 | 845 | 851 | PF00069 | 0.704 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.492 |
MOD_SUMO_for_1 | 448 | 451 | PF00179 | 0.732 |
MOD_SUMO_for_1 | 559 | 562 | PF00179 | 0.583 |
TRG_DiLeu_BaEn_1 | 95 | 100 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.806 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.674 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.800 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 583 | 585 | PF00400 | 0.757 |
TRG_Pf-PMV_PEXEL_1 | 177 | 182 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD19 | Leptomonas seymouri | 42% | 98% |
A4HGQ4 | Leishmania braziliensis | 66% | 98% |
A4I3S8 | Leishmania infantum | 99% | 100% |
E9B020 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
Q4Q866 | Leishmania major | 90% | 100% |