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 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q866
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:0006996 | organelle organization | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0034389 | lipid droplet organization | 5 | 2 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0042592 | homeostatic process | 3 | 2 |
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:0046777 | protein autophosphorylation | 6 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0055088 | lipid homeostasis | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
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: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:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004645 | 1,4-alpha-oligoglucan phosphorylase activity | 5 | 2 |
GO:0016758 | hexosyltransferase activity | 4 | 2 |
GO:0102250 | linear malto-oligosaccharide phosphorylase activity | 5 | 2 |
GO:0102499 | SHG alpha-glucan phosphorylase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.222 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 739 | 741 | PF00082 | 0.505 |
CLV_PCSK_PC7_1 | 556 | 562 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.499 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.460 |
DEG_SCF_FBW7_1 | 15 | 21 | PF00400 | 0.500 |
DEG_SPOP_SBC_1 | 627 | 631 | PF00917 | 0.616 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.500 |
DOC_CKS1_1 | 580 | 585 | PF01111 | 0.627 |
DOC_CYCLIN_RxL_1 | 139 | 152 | PF00134 | 0.469 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 323 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 396 | 407 | PF00069 | 0.707 |
DOC_MAPK_gen_1 | 524 | 534 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 570 | 578 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 560 | 568 | PF00069 | 0.583 |
DOC_MAPK_NFAT4_5 | 561 | 569 | PF00069 | 0.547 |
DOC_MAPK_RevD_3 | 546 | 561 | PF00069 | 0.284 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.636 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.572 |
DOC_PP2B_LxvP_1 | 731 | 734 | PF13499 | 0.708 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 811 | 815 | PF00917 | 0.667 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.469 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 846 | 851 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 396 | 404 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 442 | 452 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 525 | 531 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 585 | 591 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 650 | 654 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 707 | 712 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 775 | 783 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 803 | 812 | PF00244 | 0.679 |
LIG_Actin_WH2_2 | 569 | 587 | PF00022 | 0.549 |
LIG_APCC_ABBAyCdc20_2 | 157 | 163 | PF00400 | 0.516 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.513 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.738 |
LIG_eIF4E_1 | 142 | 148 | PF01652 | 0.514 |
LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.469 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.580 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.469 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.582 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.489 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.429 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.620 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.634 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.383 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.726 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.535 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.654 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.469 |
LIG_GBD_Chelix_1 | 551 | 559 | PF00786 | 0.369 |
LIG_Integrin_RGD_1 | 244 | 246 | PF01839 | 0.316 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 458 | 465 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 484 | 495 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 574 | 583 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 866 | 871 | PF02991 | 0.689 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.617 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.469 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.502 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.484 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.684 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.647 |
LIG_SH2_SRC | 840 | 843 | PF00017 | 0.672 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.691 |
LIG_SH2_STAT3 | 143 | 146 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.689 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.469 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.472 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.644 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.692 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.785 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.674 |
LIG_SH3_3 | 778 | 784 | PF00018 | 0.727 |
LIG_SH3_3 | 785 | 791 | PF00018 | 0.718 |
LIG_SH3_3 | 847 | 853 | PF00018 | 0.678 |
LIG_SH3_CIN85_PxpxPR_1 | 674 | 679 | PF14604 | 0.700 |
LIG_SUMO_SIM_anti_2 | 98 | 105 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 248 | 258 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.728 |
LIG_SxIP_EBH_1 | 626 | 639 | PF03271 | 0.650 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.704 |
LIG_UBA3_1 | 563 | 570 | PF00899 | 0.531 |
LIG_WRC_WIRS_1 | 465 | 470 | PF05994 | 0.603 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.585 |
MOD_CDK_SPxK_1 | 579 | 585 | PF00069 | 0.615 |
MOD_CDK_SPxK_1 | 807 | 813 | PF00069 | 0.704 |
MOD_CDK_SPxxK_3 | 579 | 586 | PF00069 | 0.670 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.679 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.475 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.691 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.696 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.718 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.653 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.634 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.718 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.551 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.654 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.681 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.822 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.688 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.808 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.679 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.657 |
MOD_CK1_1 | 801 | 807 | PF00069 | 0.765 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.688 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.597 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.654 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.698 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.663 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.588 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.625 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.629 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.703 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.295 |
MOD_Cter_Amidation | 522 | 525 | PF01082 | 0.396 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.290 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.284 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.376 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.497 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.481 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.433 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.413 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.260 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.489 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.454 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.462 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.494 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.482 |
MOD_GlcNHglycan | 621 | 625 | PF01048 | 0.596 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.435 |
MOD_GlcNHglycan | 727 | 731 | PF01048 | 0.543 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.465 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.514 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.491 |
MOD_GlcNHglycan | 836 | 840 | PF01048 | 0.488 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.509 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.469 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.564 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.422 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.407 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.649 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.823 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.736 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.696 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.745 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.661 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.755 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.621 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.567 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.667 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.669 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.640 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.679 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.823 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.469 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.651 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.669 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.731 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.786 |
MOD_LATS_1 | 681 | 687 | PF00433 | 0.713 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.530 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.507 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.463 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.489 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.469 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.636 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.679 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.696 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.632 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.658 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.455 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.619 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.783 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.671 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.695 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.469 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.504 |
MOD_NEK2_2 | 798 | 803 | PF00069 | 0.700 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.422 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.773 |
MOD_PIKK_1 | 699 | 705 | PF00454 | 0.819 |
MOD_PIKK_1 | 817 | 823 | PF00454 | 0.703 |
MOD_PKA_1 | 679 | 685 | PF00069 | 0.715 |
MOD_PKA_1 | 707 | 713 | PF00069 | 0.720 |
MOD_PKA_1 | 775 | 781 | PF00069 | 0.686 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.455 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.516 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.469 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.722 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.668 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.705 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.364 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.603 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.664 |
MOD_PKA_2 | 707 | 713 | PF00069 | 0.720 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.708 |
MOD_PKB_1 | 762 | 770 | PF00069 | 0.794 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.516 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.721 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.626 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.666 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.614 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.741 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.682 |
MOD_Plk_1 | 767 | 773 | PF00069 | 0.758 |
MOD_Plk_1 | 835 | 841 | PF00069 | 0.656 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.516 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.680 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.469 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.484 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.467 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.504 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.644 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.591 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.671 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.469 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.500 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.463 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.685 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.726 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.627 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.621 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.637 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.666 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.650 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.469 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.831 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.716 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.729 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.686 |
MOD_ProDKin_1 | 846 | 852 | PF00069 | 0.677 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.469 |
MOD_SUMO_for_1 | 448 | 451 | PF00179 | 0.673 |
TRG_DiLeu_BaEn_1 | 95 | 100 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.757 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 439 | 442 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 177 | 182 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD19 | Leptomonas seymouri | 43% | 98% |
A0A3Q8IE08 | Leishmania donovani | 90% | 100% |
A4HGQ4 | Leishmania braziliensis | 67% | 100% |
A4I3S8 | Leishmania infantum | 91% | 100% |
E9B020 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |