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: A4HGQ4
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 | 0.529 |
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 762 | 764 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 767 | 769 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 732 | 734 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 767 | 769 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.217 |
CLV_PCSK_PC1ET2_1 | 732 | 734 | PF00082 | 0.545 |
CLV_PCSK_PC7_1 | 630 | 636 | PF00082 | 0.360 |
CLV_PCSK_PC7_1 | 763 | 769 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.388 |
CLV_Separin_Metazoa | 208 | 212 | PF03568 | 0.469 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 772 | 780 | PF00400 | 0.643 |
DEG_SCF_FBW7_1 | 15 | 21 | PF00400 | 0.512 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.512 |
DOC_CKS1_1 | 422 | 427 | PF01111 | 0.624 |
DOC_CKS1_1 | 571 | 576 | PF01111 | 0.640 |
DOC_CYCLIN_RxL_1 | 139 | 153 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 544 | 553 | PF00134 | 0.303 |
DOC_CYCLIN_yCln2_LP_2 | 826 | 832 | PF00134 | 0.629 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 551 | 559 | PF00069 | 0.620 |
DOC_PP2B_LxvP_1 | 423 | 426 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.606 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 722 | 725 | PF13499 | 0.735 |
DOC_PP4_MxPP_1 | 620 | 623 | PF00568 | 0.614 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 683 | 687 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 728 | 732 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 799 | 803 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.829 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 307 | 314 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 414 | 423 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 431 | 439 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 518 | 522 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 579 | 589 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 767 | 775 | PF00244 | 0.692 |
LIG_Actin_WH2_2 | 416 | 433 | PF00022 | 0.630 |
LIG_Actin_WH2_2 | 95 | 113 | PF00022 | 0.417 |
LIG_APCC_ABBAyCdc20_2 | 157 | 163 | PF00400 | 0.529 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.733 |
LIG_Clathr_ClatBox_1 | 776 | 780 | PF01394 | 0.650 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.524 |
LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.475 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.618 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.475 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.413 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.564 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.613 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.716 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.738 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.225 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.434 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.383 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.732 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.417 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.629 |
LIG_FHA_2 | 789 | 795 | PF00498 | 0.639 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.475 |
LIG_GBD_Chelix_1 | 542 | 550 | PF00786 | 0.388 |
LIG_Integrin_RGD_1 | 244 | 246 | PF01839 | 0.329 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.475 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 351 | 362 | PF02991 | 0.730 |
LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 443 | 451 | PF02991 | 0.740 |
LIG_LIR_Gen_1 | 475 | 486 | PF02991 | 0.820 |
LIG_LIR_Gen_1 | 565 | 574 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 857 | 862 | PF02991 | 0.684 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.303 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.529 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.475 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.479 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.531 |
LIG_SH2_CRK | 354 | 358 | PF00017 | 0.728 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.413 |
LIG_SH2_SRC | 831 | 834 | PF00017 | 0.678 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 143 | 146 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 831 | 834 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.475 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.427 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.481 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.629 |
LIG_SH3_3 | 679 | 685 | PF00018 | 0.785 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.646 |
LIG_SH3_3 | 735 | 741 | PF00018 | 0.670 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.733 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.724 |
LIG_SH3_3 | 838 | 844 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 248 | 258 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 600 | 606 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 147 | 153 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 248 | 258 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.747 |
LIG_SUMO_SIM_par_1 | 774 | 781 | PF11976 | 0.661 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.743 |
LIG_WRC_WIRS_1 | 566 | 571 | PF05994 | 0.615 |
MOD_CDK_SPK_2 | 372 | 377 | PF00069 | 0.653 |
MOD_CDK_SPK_2 | 768 | 773 | PF00069 | 0.644 |
MOD_CDK_SPxK_1 | 570 | 576 | PF00069 | 0.629 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 372 | 379 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 570 | 577 | PF00069 | 0.690 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.456 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.659 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.662 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.461 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.712 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.748 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.737 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.631 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.691 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.733 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.691 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.822 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.690 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.652 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.683 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.643 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.703 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.601 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.413 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.624 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.630 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.683 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.683 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.657 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.275 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.277 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.396 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.370 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.539 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.220 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.513 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.446 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.423 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.454 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.615 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.375 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.514 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.488 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.435 |
MOD_GlcNHglycan | 746 | 750 | PF01048 | 0.428 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.492 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.507 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.548 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.420 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.756 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.709 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.675 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.740 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.647 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.801 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.672 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.692 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.719 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.661 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.679 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.678 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.657 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.579 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.824 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.475 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.648 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.752 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.745 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.676 |
MOD_LATS_1 | 490 | 496 | PF00433 | 0.625 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.504 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.542 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.476 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.488 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.475 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.673 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.721 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.650 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.490 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.624 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.769 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.617 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.777 |
MOD_NEK2_2 | 150 | 155 | PF00069 | 0.413 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.475 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.475 |
MOD_NEK2_2 | 799 | 804 | PF00069 | 0.694 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.644 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.618 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.748 |
MOD_PIKK_1 | 690 | 696 | PF00454 | 0.828 |
MOD_PIKK_1 | 766 | 772 | PF00454 | 0.691 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.703 |
MOD_PK_1 | 713 | 719 | PF00069 | 0.644 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.413 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.413 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.529 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.475 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.644 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.715 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.373 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.610 |
MOD_PKA_2 | 757 | 763 | PF00069 | 0.723 |
MOD_PKA_2 | 766 | 772 | PF00069 | 0.699 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.529 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.695 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.727 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.659 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.819 |
MOD_Plk_1 | 758 | 764 | PF00069 | 0.761 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.529 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.413 |
MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.692 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.475 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.413 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.475 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.383 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.647 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.617 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.475 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.512 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.468 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.670 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.791 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.625 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.654 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.754 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.649 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.636 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.645 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.771 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.829 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.475 |
MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.735 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.678 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 105 | 113 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_1 | 95 | 100 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.725 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.759 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 633 | 635 | PF00400 | 0.556 |
TRG_NLS_MonoExtC_3 | 172 | 177 | PF00514 | 0.413 |
TRG_NLS_MonoExtC_3 | 762 | 767 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 763 | 768 | PF00514 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.217 |
TRG_Pf-PMV_PEXEL_1 | 383 | 388 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD19 | Leptomonas seymouri | 44% | 97% |
A0A3Q8IE08 | Leishmania donovani | 66% | 99% |
A4I3S8 | Leishmania infantum | 67% | 99% |
E9B020 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q866 | Leishmania major | 67% | 99% |