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: 1, no: 12 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 3 |
GO:0016020 | membrane | 2 | 12 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QD29
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 3 |
GO:0006493 | protein O-linked glycosylation | 5 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0006950 | response to stress | 2 | 3 |
GO:0007165 | signal transduction | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0030968 | endoplasmic reticulum unfolded protein response | 3 | 3 |
GO:0033554 | cellular response to stress | 3 | 3 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 3 |
GO:0035268 | protein mannosylation | 4 | 3 |
GO:0035269 | protein O-linked mannosylation | 5 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0043413 | macromolecule glycosylation | 3 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0050789 | regulation of biological process | 2 | 3 |
GO:0050794 | regulation of cellular process | 3 | 3 |
GO:0050896 | response to stimulus | 1 | 3 |
GO:0051716 | cellular response to stimulus | 2 | 3 |
GO:0065007 | biological regulation | 1 | 3 |
GO:0070085 | glycosylation | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0097502 | mannosylation | 3 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000030 | mannosyltransferase activity | 5 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016757 | glycosyltransferase activity | 3 | 4 |
GO:0016758 | hexosyltransferase activity | 4 | 4 |
GO:0004169 | dolichyl-phosphate-mannose-protein mannosyltransferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 789 | 793 | PF00656 | 0.396 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 891 | 893 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 873 | 875 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 890 | 892 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 682 | 684 | PF00082 | 0.660 |
CLV_PCSK_PC7_1 | 303 | 309 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 891 | 895 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.494 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.590 |
DEG_ODPH_VHL_1 | 743 | 755 | PF01847 | 0.346 |
DEG_SCF_TRCP1_1 | 282 | 288 | PF00400 | 0.211 |
DEG_SPOP_SBC_1 | 729 | 733 | PF00917 | 0.591 |
DOC_CDC14_PxL_1 | 476 | 484 | PF14671 | 0.522 |
DOC_CKS1_1 | 807 | 812 | PF01111 | 0.342 |
DOC_CYCLIN_RxL_1 | 351 | 361 | PF00134 | 0.341 |
DOC_CYCLIN_RxL_1 | 609 | 619 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 160 | 166 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 176 | 182 | PF00134 | 0.186 |
DOC_MAPK_gen_1 | 152 | 161 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 581 | 590 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 134 | 141 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 812 | 819 | PF00069 | 0.389 |
DOC_MAPK_RevD_3 | 313 | 328 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 609 | 616 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.349 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 897 | 901 | PF00917 | 0.460 |
DOC_USP7_UBL2_3 | 735 | 739 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 343 | 351 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 517 | 527 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 783 | 790 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 891 | 897 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 91 | 96 | PF00244 | 0.317 |
LIG_Actin_WH2_1 | 327 | 345 | PF00022 | 0.424 |
LIG_Actin_WH2_2 | 469 | 485 | PF00022 | 0.453 |
LIG_Actin_WH2_2 | 570 | 586 | PF00022 | 0.285 |
LIG_Actin_WH2_2 | 626 | 644 | PF00022 | 0.394 |
LIG_AP2alpha_2 | 596 | 598 | PF02296 | 0.368 |
LIG_APCC_ABBA_1 | 816 | 821 | PF00400 | 0.350 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_BIR_III_4 | 792 | 796 | PF00653 | 0.315 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.384 |
LIG_Clathr_ClatBox_1 | 817 | 821 | PF01394 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 510 | 519 | PF00928 | 0.309 |
LIG_deltaCOP1_diTrp_1 | 75 | 84 | PF00928 | 0.473 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.507 |
LIG_eIF4E_1 | 196 | 202 | PF01652 | 0.453 |
LIG_eIF4E_1 | 490 | 496 | PF01652 | 0.478 |
LIG_eIF4E_1 | 627 | 633 | PF01652 | 0.477 |
LIG_eIF4E_1 | 697 | 703 | PF01652 | 0.302 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.530 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.413 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.730 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.507 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.444 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.419 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.368 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.336 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.368 |
LIG_FHA_2 | 787 | 793 | PF00498 | 0.367 |
LIG_FHA_2 | 803 | 809 | PF00498 | 0.433 |
LIG_Integrin_RGD_1 | 44 | 46 | PF01839 | 0.502 |
LIG_IRF3_LxIS_1 | 156 | 162 | PF10401 | 0.446 |
LIG_LIR_Apic_2 | 772 | 778 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 605 | 615 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 626 | 633 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 70 | 81 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 764 | 773 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 785 | 794 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 855 | 866 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 902 | 908 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 567 | 572 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 626 | 630 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 764 | 769 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 785 | 790 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 855 | 861 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 902 | 908 | PF02991 | 0.335 |
LIG_LRP6_Inhibitor_1 | 38 | 44 | PF00058 | 0.329 |
LIG_NRBOX | 155 | 161 | PF00104 | 0.529 |
LIG_NRBOX | 410 | 416 | PF00104 | 0.424 |
LIG_NRBOX | 432 | 438 | PF00104 | 0.399 |
LIG_OCRL_FandH_1 | 203 | 215 | PF00620 | 0.545 |
LIG_PDZ_Class_2 | 903 | 908 | PF00595 | 0.422 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.372 |
LIG_Pex14_1 | 17 | 21 | PF04695 | 0.594 |
LIG_Pex14_2 | 113 | 117 | PF04695 | 0.388 |
LIG_Pex14_2 | 326 | 330 | PF04695 | 0.445 |
LIG_Pex14_2 | 72 | 76 | PF04695 | 0.381 |
LIG_PTB_Apo_2 | 344 | 351 | PF02174 | 0.298 |
LIG_PTB_Apo_2 | 689 | 696 | PF02174 | 0.362 |
LIG_PTB_Apo_2 | 832 | 839 | PF02174 | 0.350 |
LIG_PTB_Phospho_1 | 344 | 350 | PF10480 | 0.298 |
LIG_PTB_Phospho_1 | 689 | 695 | PF10480 | 0.363 |
LIG_PTB_Phospho_1 | 832 | 838 | PF10480 | 0.292 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.405 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.303 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.405 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.507 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.326 |
LIG_SH2_CRK | 627 | 631 | PF00017 | 0.350 |
LIG_SH2_CRK | 775 | 779 | PF00017 | 0.504 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.394 |
LIG_SH2_GRB2like | 123 | 126 | PF00017 | 0.507 |
LIG_SH2_GRB2like | 801 | 804 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 775 | 779 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 136 | 139 | PF00017 | 0.455 |
LIG_SH2_PTP2 | 587 | 590 | PF00017 | 0.288 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.496 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.397 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.405 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.176 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 690 | 693 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 801 | 804 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.418 |
LIG_SH3_1 | 739 | 745 | PF00018 | 0.524 |
LIG_SH3_1 | 775 | 781 | PF00018 | 0.458 |
LIG_SH3_2 | 778 | 783 | PF14604 | 0.449 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.476 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.336 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.453 |
LIG_SH3_3 | 739 | 745 | PF00018 | 0.494 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.458 |
LIG_SPRY_1 | 576 | 581 | PF00622 | 0.326 |
LIG_SUMO_SIM_anti_2 | 29 | 35 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 426 | 432 | PF11976 | 0.621 |
LIG_SUMO_SIM_anti_2 | 629 | 635 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 814 | 819 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 469 | 474 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.394 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.516 |
LIG_TYR_ITIM | 121 | 126 | PF00017 | 0.507 |
LIG_TYR_ITIM | 417 | 422 | PF00017 | 0.303 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.371 |
LIG_TYR_ITIM | 625 | 630 | PF00017 | 0.408 |
LIG_TYR_ITIM | 802 | 807 | PF00017 | 0.424 |
LIG_TYR_ITSM | 783 | 790 | PF00017 | 0.610 |
LIG_UBA3_1 | 274 | 281 | PF00899 | 0.351 |
LIG_UBA3_1 | 630 | 637 | PF00899 | 0.446 |
LIG_WRC_WIRS_1 | 453 | 458 | PF05994 | 0.516 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.405 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.398 |
MOD_CDK_SPxK_1 | 806 | 812 | PF00069 | 0.599 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.488 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.361 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.502 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.797 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.269 |
MOD_CK1_1 | 895 | 901 | PF00069 | 0.490 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.440 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.458 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.525 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.519 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.719 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.597 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.405 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.413 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.420 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.695 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.545 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.604 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.692 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.418 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.443 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.435 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.342 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.386 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.619 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.452 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.758 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.511 |
MOD_GSK3_1 | 802 | 809 | PF00069 | 0.504 |
MOD_GSK3_1 | 842 | 849 | PF00069 | 0.343 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.460 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.471 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.289 |
MOD_N-GLC_1 | 616 | 621 | PF02516 | 0.469 |
MOD_N-GLC_1 | 669 | 674 | PF02516 | 0.516 |
MOD_N-GLC_1 | 802 | 807 | PF02516 | 0.550 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.414 |
MOD_N-GLC_1 | 876 | 881 | PF02516 | 0.608 |
MOD_N-GLC_2 | 125 | 127 | PF02516 | 0.405 |
MOD_N-GLC_2 | 601 | 603 | PF02516 | 0.381 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.402 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.361 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.376 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.320 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.370 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.504 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.426 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.392 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.397 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.504 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.572 |
MOD_NEK2_2 | 289 | 294 | PF00069 | 0.434 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.512 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.383 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.504 |
MOD_PIKK_1 | 669 | 675 | PF00454 | 0.356 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.421 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.507 |
MOD_PK_1 | 543 | 549 | PF00069 | 0.378 |
MOD_PKA_1 | 682 | 688 | PF00069 | 0.543 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.320 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.628 |
MOD_PKA_2 | 782 | 788 | PF00069 | 0.547 |
MOD_PKB_1 | 890 | 898 | PF00069 | 0.330 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.458 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.371 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.476 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.392 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.316 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.613 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.543 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.607 |
MOD_Plk_1 | 820 | 826 | PF00069 | 0.518 |
MOD_Plk_1 | 901 | 907 | PF00069 | 0.420 |
MOD_Plk_2-3 | 511 | 517 | PF00069 | 0.394 |
MOD_Plk_2-3 | 620 | 626 | PF00069 | 0.415 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.439 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.430 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.496 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.515 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.496 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.523 |
MOD_Plk_4 | 829 | 835 | PF00069 | 0.448 |
MOD_Plk_4 | 901 | 907 | PF00069 | 0.405 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.519 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.453 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.487 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 681 | 684 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 558 | 565 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 60 | 68 | PF00179 | 0.293 |
TRG_AP2beta_CARGO_1 | 855 | 865 | PF09066 | 0.337 |
TRG_DiLeu_BaEn_1 | 620 | 625 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.303 |
TRG_DiLeu_BaLyEn_6 | 337 | 342 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 787 | 790 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 804 | 807 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 827 | 830 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 872 | 874 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 890 | 892 | PF00400 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJE2 | Leptomonas seymouri | 60% | 99% |
A0A0S4JIN2 | Bodo saltans | 30% | 100% |
A0A1X0NWI5 | Trypanosomatidae | 32% | 98% |
A0A3S5H779 | Leishmania donovani | 93% | 100% |
A0A3S7WX22 | Leishmania donovani | 63% | 100% |
A4HBI3 | Leishmania braziliensis | 78% | 100% |
A4HC73 | Leishmania braziliensis | 61% | 100% |
A4HYK6 | Leishmania infantum | 93% | 100% |
A4HZP9 | Leishmania infantum | 63% | 100% |
E9AUF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AVK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QBX4 | Leishmania major | 61% | 98% |