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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005759 | mitochondrial matrix | 5 | 2 |
GO:0005782 | peroxisomal matrix | 6 | 2 |
GO:0031907 | microbody lumen | 5 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QIL8
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006084 | acetyl-CoA metabolic process | 5 | 2 |
GO:0006085 | acetyl-CoA biosynthetic process | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006163 | purine nucleotide metabolic process | 5 | 2 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 2 |
GO:0006195 | purine nucleotide catabolic process | 6 | 2 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006631 | fatty acid metabolic process | 4 | 12 |
GO:0006633 | fatty acid biosynthetic process | 5 | 12 |
GO:0006637 | acyl-CoA metabolic process | 4 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 2 |
GO:0006790 | sulfur compound metabolic process | 3 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009117 | nucleotide metabolic process | 5 | 2 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 2 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 2 |
GO:0009154 | purine ribonucleotide catabolic process | 6 | 2 |
GO:0009165 | nucleotide biosynthetic process | 6 | 2 |
GO:0009166 | nucleotide catabolic process | 6 | 2 |
GO:0009259 | ribonucleotide metabolic process | 5 | 2 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 2 |
GO:0009261 | ribonucleotide catabolic process | 5 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010565 | regulation of cellular ketone metabolic process | 5 | 2 |
GO:0016053 | organic acid biosynthetic process | 4 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019216 | regulation of lipid metabolic process | 5 | 2 |
GO:0019217 | regulation of fatty acid metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0019693 | ribose phosphate metabolic process | 4 | 2 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 12 |
GO:0033865 | nucleoside bisphosphate metabolic process | 5 | 2 |
GO:0033866 | nucleoside bisphosphate biosynthetic process | 6 | 2 |
GO:0033869 | nucleoside bisphosphate catabolic process | 6 | 2 |
GO:0033875 | ribonucleoside bisphosphate metabolic process | 6 | 2 |
GO:0034030 | ribonucleoside bisphosphate biosynthetic process | 7 | 2 |
GO:0034031 | ribonucleoside bisphosphate catabolic process | 7 | 2 |
GO:0034032 | purine nucleoside bisphosphate metabolic process | 5 | 2 |
GO:0034033 | purine nucleoside bisphosphate biosynthetic process | 6 | 2 |
GO:0034034 | purine nucleoside bisphosphate catabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0035383 | thioester metabolic process | 3 | 2 |
GO:0035384 | thioester biosynthetic process | 4 | 2 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 2 |
GO:0044273 | sulfur compound catabolic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0044283 | small molecule biosynthetic process | 3 | 12 |
GO:0045834 | positive regulation of lipid metabolic process | 5 | 2 |
GO:0045923 | positive regulation of fatty acid metabolic process | 6 | 2 |
GO:0046320 | regulation of fatty acid oxidation | 7 | 2 |
GO:0046321 | positive regulation of fatty acid oxidation | 7 | 2 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 2 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 12 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0062012 | regulation of small molecule metabolic process | 4 | 2 |
GO:0062013 | positive regulation of small molecule metabolic process | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071616 | acyl-CoA biosynthetic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 12 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 2 |
GO:0072523 | purine-containing compound catabolic process | 5 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 2 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 2 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:2001293 | malonyl-CoA metabolic process | 5 | 2 |
GO:2001294 | malonyl-CoA catabolic process | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016829 | lyase activity | 2 | 12 |
GO:0016830 | carbon-carbon lyase activity | 3 | 12 |
GO:0016831 | carboxy-lyase activity | 4 | 12 |
GO:0050080 | malonyl-CoA decarboxylase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 714 | 716 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.560 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.510 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.748 |
DEG_SCF_FBW7_1 | 549 | 554 | PF00400 | 0.562 |
DEG_SPOP_SBC_1 | 634 | 638 | PF00917 | 0.400 |
DEG_SPOP_SBC_1 | 676 | 680 | PF00917 | 0.359 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 784 | 792 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 162 | 165 | PF00134 | 0.543 |
DOC_CYCLIN_yCln2_LP_2 | 698 | 704 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 748 | 758 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 360 | 368 | PF00069 | 0.470 |
DOC_PP1_RVXF_1 | 736 | 742 | PF00149 | 0.517 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 698 | 701 | PF13499 | 0.547 |
DOC_PP2B_PxIxI_1 | 443 | 449 | PF00149 | 0.487 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.693 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.709 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 747 | 751 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.341 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 229 | 238 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 42 | 48 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 544 | 550 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 639 | 647 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.663 |
LIG_Actin_WH2_2 | 124 | 139 | PF00022 | 0.571 |
LIG_Actin_WH2_2 | 205 | 222 | PF00022 | 0.567 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 587 | 591 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_2 | 587 | 593 | PF00533 | 0.507 |
LIG_CtBP_PxDLS_1 | 521 | 527 | PF00389 | 0.581 |
LIG_deltaCOP1_diTrp_1 | 153 | 159 | PF00928 | 0.531 |
LIG_EVH1_1 | 53 | 57 | PF00568 | 0.725 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.662 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.553 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.438 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.481 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.574 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.487 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.442 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.582 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.477 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.539 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.480 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.559 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.628 |
LIG_LIR_Apic_2 | 112 | 118 | PF02991 | 0.677 |
LIG_LIR_Apic_2 | 601 | 607 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 153 | 164 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 182 | 191 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 382 | 391 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 554 | 563 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 554 | 558 | PF02991 | 0.488 |
LIG_MYND_1 | 51 | 55 | PF01753 | 0.722 |
LIG_NRBOX | 390 | 396 | PF00104 | 0.414 |
LIG_NRBOX | 652 | 658 | PF00104 | 0.506 |
LIG_PCNA_yPIPBox_3 | 520 | 533 | PF02747 | 0.491 |
LIG_PROFILIN_1 | 48 | 54 | PF00235 | 0.679 |
LIG_PTB_Apo_2 | 375 | 382 | PF02174 | 0.321 |
LIG_PTB_Apo_2 | 756 | 763 | PF02174 | 0.476 |
LIG_PTB_Phospho_1 | 756 | 762 | PF10480 | 0.476 |
LIG_SH2_CRK | 762 | 766 | PF00017 | 0.612 |
LIG_SH2_NCK_1 | 762 | 766 | PF00017 | 0.603 |
LIG_SH2_PTP2 | 215 | 218 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.476 |
LIG_SH3_1 | 45 | 51 | PF00018 | 0.715 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.734 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.530 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.486 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.715 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.641 |
LIG_SxIP_EBH_1 | 554 | 566 | PF03271 | 0.553 |
LIG_TRAF2_1 | 597 | 600 | PF00917 | 0.596 |
LIG_TRAF2_2 | 118 | 123 | PF00917 | 0.689 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.443 |
LIG_UBA3_1 | 248 | 256 | PF00899 | 0.471 |
LIG_UBA3_1 | 376 | 383 | PF00899 | 0.544 |
LIG_WRC_WIRS_1 | 552 | 557 | PF05994 | 0.344 |
LIG_WRC_WIRS_1 | 671 | 676 | PF05994 | 0.535 |
LIG_WW_2 | 51 | 54 | PF00397 | 0.719 |
MOD_CDK_SPK_2 | 743 | 748 | PF00069 | 0.398 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.625 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.619 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.681 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.544 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.514 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.363 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.324 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.728 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.394 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.461 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.328 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.557 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.670 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.530 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.625 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.664 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.653 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.560 |
MOD_DYRK1A_RPxSP_1 | 547 | 551 | PF00069 | 0.449 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.708 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.638 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.520 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.663 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.705 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.649 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.462 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.548 |
MOD_GlcNHglycan | 488 | 492 | PF01048 | 0.425 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.360 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.558 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.565 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.359 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.334 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.407 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.713 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.622 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.367 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.704 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.509 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.550 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.571 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.530 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.328 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.342 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.549 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.486 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.634 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.475 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.340 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.293 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.585 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.535 |
MOD_LATS_1 | 293 | 299 | PF00433 | 0.521 |
MOD_LATS_1 | 308 | 314 | PF00433 | 0.534 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.608 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.449 |
MOD_N-GLC_1 | 640 | 645 | PF02516 | 0.363 |
MOD_N-GLC_1 | 743 | 748 | PF02516 | 0.328 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.616 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.495 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.430 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.506 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.609 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.481 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.531 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.307 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.344 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.344 |
MOD_NEK2_2 | 709 | 714 | PF00069 | 0.242 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.519 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.606 |
MOD_PIKK_1 | 678 | 684 | PF00454 | 0.320 |
MOD_PK_1 | 406 | 412 | PF00069 | 0.475 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.516 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.612 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.474 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.344 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.554 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.558 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.344 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.535 |
MOD_Plk_1 | 690 | 696 | PF00069 | 0.359 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.640 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.478 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.530 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.424 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.479 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.252 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.374 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.475 |
MOD_Plk_4 | 732 | 738 | PF00069 | 0.344 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.493 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.701 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.504 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.460 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.326 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.344 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.350 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.298 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.598 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.449 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.627 |
MOD_SUMO_for_1 | 255 | 258 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 390 | 395 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 441 | 446 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 524 | 529 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 652 | 657 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 698 | 703 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 415 | 419 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 655 | 659 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF8 | Leptomonas seymouri | 55% | 100% |
A0A0S4J4K1 | Bodo saltans | 31% | 100% |
A0A1X0NPQ8 | Trypanosomatidae | 39% | 100% |
A0A3R7N686 | Trypanosoma rangeli | 39% | 100% |
A0A3S5H5Z5 | Leishmania donovani | 91% | 100% |
A4H525 | Leishmania braziliensis | 77% | 100% |
A4HT98 | Leishmania infantum | 91% | 100% |
C9ZUM4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AL87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BY47 | Trypanosoma cruzi | 43% | 100% |