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 |
Related structures:
AlphaFold database: Q4Q414
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009895 | negative regulation of catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0010628 | positive regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016553 | base conversion or substitution editing | 6 | 2 |
GO:0016554 | cytidine to uridine editing | 7 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043487 | regulation of RNA stability | 3 | 2 |
GO:0043488 | regulation of mRNA stability | 4 | 2 |
GO:0043489 | RNA stabilization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0048255 | mRNA stabilization | 5 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 2 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 2 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 2 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.397 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 641 | 645 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 879 | 883 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 761 | 763 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 809 | 811 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 851 | 853 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 860 | 862 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 761 | 763 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 809 | 811 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 860 | 862 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 723 | 725 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 772 | 776 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 836 | 840 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 634 | 638 | PF03568 | 0.525 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.471 |
DEG_APCC_DBOX_1 | 585 | 593 | PF00400 | 0.372 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.487 |
DEG_SCF_FBW7_1 | 774 | 779 | PF00400 | 0.461 |
DEG_SCF_FBW7_2 | 618 | 623 | PF00400 | 0.544 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.402 |
DOC_ANK_TNKS_1 | 479 | 486 | PF00023 | 0.583 |
DOC_CDC14_PxL_1 | 342 | 350 | PF14671 | 0.522 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.670 |
DOC_CKS1_1 | 115 | 120 | PF01111 | 0.366 |
DOC_CKS1_1 | 754 | 759 | PF01111 | 0.476 |
DOC_CKS1_1 | 773 | 778 | PF01111 | 0.526 |
DOC_CKS1_1 | 820 | 825 | PF01111 | 0.446 |
DOC_CKS1_1 | 829 | 834 | PF01111 | 0.378 |
DOC_CYCLIN_RxL_1 | 416 | 426 | PF00134 | 0.338 |
DOC_CYCLIN_RxL_1 | 833 | 843 | PF00134 | 0.396 |
DOC_CYCLIN_yCln2_LP_2 | 754 | 760 | PF00134 | 0.458 |
DOC_MAPK_DCC_7 | 444 | 454 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 498 | 507 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 884 | 892 | PF00069 | 0.613 |
DOC_PP2B_LxvP_1 | 387 | 390 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.423 |
DOC_PP4_FxxP_1 | 773 | 776 | PF00568 | 0.321 |
DOC_PP4_FxxP_1 | 820 | 823 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 883 | 887 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.509 |
DOC_USP7_MATH_2 | 558 | 564 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 681 | 685 | PF12436 | 0.422 |
DOC_USP7_UBL2_3 | 795 | 799 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 819 | 824 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.378 |
LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 513 | 522 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 637 | 646 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 698 | 704 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 766 | 774 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 827 | 832 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 884 | 892 | PF00244 | 0.576 |
LIG_14-3-3_CterR_2 | 891 | 893 | PF00244 | 0.629 |
LIG_Actin_WH2_2 | 745 | 763 | PF00022 | 0.477 |
LIG_APCC_ABBA_1 | 34 | 39 | PF00400 | 0.431 |
LIG_BIR_III_4 | 180 | 184 | PF00653 | 0.417 |
LIG_CSL_BTD_1 | 115 | 118 | PF09270 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 347 | 354 | PF00928 | 0.488 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.554 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.413 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.583 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.521 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.483 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.258 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.407 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.424 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.470 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.461 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.388 |
LIG_FHA_1 | 871 | 877 | PF00498 | 0.423 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.360 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.511 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.521 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.514 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.515 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.536 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.354 |
LIG_FHA_2 | 745 | 751 | PF00498 | 0.391 |
LIG_FHA_2 | 773 | 779 | PF00498 | 0.462 |
LIG_FHA_2 | 877 | 883 | PF00498 | 0.648 |
LIG_HCF-1_HBM_1 | 664 | 667 | PF13415 | 0.473 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 502 | 511 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 540 | 551 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 606 | 614 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 627 | 636 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 651 | 660 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 717 | 725 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 731 | 742 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 502 | 507 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 581 | 585 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 606 | 611 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 627 | 632 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 651 | 656 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 717 | 722 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.500 |
LIG_LYPXL_yS_3 | 345 | 348 | PF13949 | 0.535 |
LIG_LYPXL_yS_3 | 582 | 585 | PF13949 | 0.383 |
LIG_PCNA_TLS_4 | 498 | 505 | PF02747 | 0.391 |
LIG_Pex14_1 | 350 | 354 | PF04695 | 0.460 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.350 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.488 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.500 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.401 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.482 |
LIG_SH3_3 | 831 | 837 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 337 | 342 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 160 | 167 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 333 | 339 | PF11976 | 0.455 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.354 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.526 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.510 |
LIG_UBA3_1 | 745 | 751 | PF00899 | 0.459 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.480 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.465 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.467 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.539 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.335 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.534 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.498 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.447 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.558 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.514 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.346 |
MOD_CK1_1 | 727 | 733 | PF00069 | 0.531 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.432 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.529 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.539 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.412 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.531 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.542 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.380 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.369 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.371 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.371 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.440 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.504 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.536 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.715 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.403 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.505 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.337 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.585 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.330 |
MOD_GlcNHglycan | 861 | 864 | PF01048 | 0.288 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.486 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.522 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.391 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.378 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.489 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.446 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.574 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.708 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.591 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.563 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.369 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.200 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.324 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.540 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.478 |
MOD_LATS_1 | 127 | 133 | PF00433 | 0.381 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.463 |
MOD_N-GLC_2 | 274 | 276 | PF02516 | 0.385 |
MOD_N-GLC_2 | 407 | 409 | PF02516 | 0.459 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.535 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.283 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.384 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.453 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.390 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.383 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.442 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.517 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.562 |
MOD_NEK2_2 | 718 | 723 | PF00069 | 0.371 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.574 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.415 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.500 |
MOD_PIKK_1 | 845 | 851 | PF00454 | 0.427 |
MOD_PKA_1 | 129 | 135 | PF00069 | 0.391 |
MOD_PKA_1 | 723 | 729 | PF00069 | 0.257 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.439 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.508 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.568 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.472 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.587 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.550 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.467 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.462 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.332 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.468 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.400 |
MOD_PKA_2 | 883 | 889 | PF00069 | 0.581 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.469 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.378 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.418 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.382 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.477 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.522 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.269 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.442 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.393 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.522 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.364 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.372 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.445 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.521 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.553 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.451 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.493 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.373 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.456 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.255 |
MOD_ProDKin_1 | 819 | 825 | PF00069 | 0.438 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.372 |
MOD_SUMO_rev_2 | 388 | 397 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 663 | 668 | PF00179 | 0.343 |
TRG_DiLeu_BaEn_1 | 732 | 737 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_2 | 292 | 298 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_2 | 768 | 774 | PF01217 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 834 | 839 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 636 | 639 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 760 | 762 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 809 | 811 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 859 | 861 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 874 | 876 | PF00400 | 0.453 |
TRG_NES_CRM1_1 | 292 | 307 | PF08389 | 0.380 |
TRG_NES_CRM1_1 | 499 | 510 | PF08389 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 306 | 310 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 836 | 841 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 866 | 870 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAS6 | Leptomonas seymouri | 60% | 98% |
A0A0S4JFF4 | Bodo saltans | 34% | 85% |
A0A1X0P174 | Trypanosomatidae | 41% | 100% |
A0A3Q8IHV0 | Leishmania donovani | 95% | 100% |
A0A3R7M0F7 | Trypanosoma rangeli | 41% | 100% |
A4HLN4 | Leishmania braziliensis | 90% | 99% |
A4I969 | Leishmania infantum | 95% | 100% |
C9ZIW5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B410 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5AXB1 | Trypanosoma cruzi | 43% | 100% |