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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9A7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 851 | 855 | PF00656 | 0.366 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 982 | 984 | PF00675 | 0.449 |
CLV_PCSK_FUR_1 | 797 | 801 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 846 | 848 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 982 | 984 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 799 | 801 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 846 | 848 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 841 | 845 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 870 | 874 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.406 |
DEG_COP1_1 | 292 | 304 | PF00400 | 0.476 |
DEG_Kelch_Keap1_1 | 146 | 151 | PF01344 | 0.317 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.531 |
DOC_CDC14_PxL_1 | 160 | 168 | PF14671 | 0.281 |
DOC_CKS1_1 | 495 | 500 | PF01111 | 0.416 |
DOC_CYCLIN_RxL_1 | 313 | 322 | PF00134 | 0.534 |
DOC_CYCLIN_RxL_1 | 62 | 73 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 89 | 95 | PF00134 | 0.402 |
DOC_MAPK_DCC_7 | 161 | 171 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 124 | 134 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 453 | 461 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 314 | 321 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.409 |
DOC_PP1_RVXF_1 | 844 | 851 | PF00149 | 0.366 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.241 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.352 |
DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.255 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.161 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 729 | 734 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 280 | 286 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 525 | 533 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 71 | 81 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 718 | 726 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 797 | 807 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 847 | 856 | PF00244 | 0.385 |
LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.396 |
LIG_Actin_WH2_2 | 38 | 56 | PF00022 | 0.398 |
LIG_APCC_ABBA_1 | 390 | 395 | PF00400 | 0.304 |
LIG_APCC_ABBA_1 | 466 | 471 | PF00400 | 0.310 |
LIG_BIR_III_4 | 303 | 307 | PF00653 | 0.240 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.358 |
LIG_BRCT_BRCA1_1 | 662 | 666 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 738 | 742 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 962 | 966 | PF00533 | 0.347 |
LIG_BRCT_BRCA1_2 | 962 | 968 | PF00533 | 0.378 |
LIG_EH1_1 | 111 | 119 | PF00400 | 0.349 |
LIG_FAT_LD_1 | 478 | 486 | PF03623 | 0.382 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.598 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.548 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.492 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.421 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.396 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.385 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.379 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.358 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.390 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.290 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.263 |
LIG_FHA_1 | 774 | 780 | PF00498 | 0.291 |
LIG_FHA_1 | 809 | 815 | PF00498 | 0.368 |
LIG_FHA_1 | 843 | 849 | PF00498 | 0.389 |
LIG_FHA_1 | 860 | 866 | PF00498 | 0.369 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.404 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.287 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.403 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.288 |
LIG_FHA_2 | 722 | 728 | PF00498 | 0.430 |
LIG_FHA_2 | 834 | 840 | PF00498 | 0.546 |
LIG_LIR_Gen_1 | 205 | 213 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 312 | 320 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 427 | 435 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 444 | 455 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 500 | 507 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 654 | 665 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 669 | 679 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 723 | 733 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 739 | 750 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 776 | 781 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 809 | 819 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 920 | 928 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 564 | 570 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 599 | 605 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 654 | 660 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 669 | 675 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 739 | 745 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 776 | 780 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 885 | 890 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 920 | 924 | PF02991 | 0.388 |
LIG_LRP6_Inhibitor_1 | 132 | 138 | PF00058 | 0.264 |
LIG_MYND_1 | 164 | 168 | PF01753 | 0.436 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.226 |
LIG_PCNA_PIPBox_1 | 78 | 87 | PF02747 | 0.364 |
LIG_PCNA_yPIPBox_3 | 108 | 118 | PF02747 | 0.366 |
LIG_PCNA_yPIPBox_3 | 687 | 696 | PF02747 | 0.461 |
LIG_Pex14_1 | 981 | 985 | PF04695 | 0.443 |
LIG_Pex14_2 | 240 | 244 | PF04695 | 0.360 |
LIG_Rb_pABgroove_1 | 720 | 728 | PF01858 | 0.352 |
LIG_Rb_pABgroove_1 | 826 | 834 | PF01858 | 0.379 |
LIG_REV1ctd_RIR_1 | 241 | 249 | PF16727 | 0.447 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.353 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.388 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.317 |
LIG_SH2_CRK | 567 | 571 | PF00017 | 0.376 |
LIG_SH2_CRK | 637 | 641 | PF00017 | 0.367 |
LIG_SH2_CRK | 777 | 781 | PF00017 | 0.335 |
LIG_SH2_CRK | 887 | 891 | PF00017 | 0.425 |
LIG_SH2_CRK | 921 | 925 | PF00017 | 0.368 |
LIG_SH2_CRK | 985 | 989 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 519 | 523 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 985 | 989 | PF00017 | 0.600 |
LIG_SH2_SRC | 519 | 522 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 985 | 989 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 679 | 682 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 770 | 773 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 812 | 815 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 887 | 890 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 894 | 897 | PF00017 | 0.302 |
LIG_SH3_1 | 697 | 703 | PF00018 | 0.467 |
LIG_SH3_3 | 697 | 703 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 197 | 205 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 130 | 136 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 197 | 205 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 77 | 83 | PF11976 | 0.363 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.465 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.433 |
LIG_TRAF2_1 | 836 | 839 | PF00917 | 0.564 |
LIG_TYR_ITAM | 774 | 793 | PF00017 | 0.318 |
LIG_TYR_ITIM | 426 | 431 | PF00017 | 0.419 |
LIG_TYR_ITIM | 775 | 780 | PF00017 | 0.335 |
LIG_TYR_ITIM | 919 | 924 | PF00017 | 0.391 |
LIG_UBA3_1 | 118 | 127 | PF00899 | 0.228 |
LIG_UBA3_1 | 152 | 161 | PF00899 | 0.500 |
LIG_UBA3_1 | 481 | 487 | PF00899 | 0.368 |
LIG_UBA3_1 | 537 | 545 | PF00899 | 0.546 |
LIG_UBA3_1 | 570 | 576 | PF00899 | 0.418 |
LIG_UBA3_1 | 725 | 730 | PF00899 | 0.335 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.408 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.413 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.423 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.507 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.442 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.402 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.412 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.391 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.347 |
MOD_CK2_1 | 833 | 839 | PF00069 | 0.533 |
MOD_CK2_1 | 992 | 998 | PF00069 | 0.431 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.577 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.367 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.445 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.340 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.547 |
MOD_GlcNHglycan | 352 | 356 | PF01048 | 0.416 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.308 |
MOD_GlcNHglycan | 631 | 635 | PF01048 | 0.433 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.314 |
MOD_GlcNHglycan | 800 | 803 | PF01048 | 0.417 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.389 |
MOD_GlcNHglycan | 850 | 853 | PF01048 | 0.410 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.409 |
MOD_GlcNHglycan | 882 | 885 | PF01048 | 0.324 |
MOD_GlcNHglycan | 962 | 965 | PF01048 | 0.381 |
MOD_GlcNHglycan | 990 | 993 | PF01048 | 0.589 |
MOD_GlcNHglycan | 994 | 997 | PF01048 | 0.569 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.479 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.446 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.421 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.469 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.343 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.373 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.422 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.430 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.373 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.277 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.493 |
MOD_GSK3_1 | 878 | 885 | PF00069 | 0.419 |
MOD_GSK3_1 | 988 | 995 | PF00069 | 0.577 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.457 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.554 |
MOD_N-GLC_1 | 683 | 688 | PF02516 | 0.486 |
MOD_N-GLC_1 | 773 | 778 | PF02516 | 0.419 |
MOD_N-GLC_1 | 859 | 864 | PF02516 | 0.548 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.308 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.372 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.579 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.478 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.300 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.469 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.322 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.368 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.487 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.438 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.342 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.445 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.351 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.288 |
MOD_NEK2_1 | 960 | 965 | PF00069 | 0.380 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.529 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.470 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.380 |
MOD_PK_1 | 591 | 597 | PF00069 | 0.533 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.410 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.355 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.409 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.333 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.498 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.139 |
MOD_Plk_1 | 773 | 779 | PF00069 | 0.382 |
MOD_Plk_1 | 808 | 814 | PF00069 | 0.414 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.357 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.523 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.457 |
MOD_Plk_2-3 | 322 | 328 | PF00069 | 0.426 |
MOD_Plk_2-3 | 721 | 727 | PF00069 | 0.274 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.332 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.336 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.391 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.337 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.405 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.283 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.366 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.458 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.281 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.285 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.655 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.161 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.415 |
MOD_ProDKin_1 | 729 | 735 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 590 | 593 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 292 | 298 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 723 | 732 | PF00179 | 0.288 |
TRG_DiLeu_BaEn_1 | 620 | 625 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_1 | 839 | 844 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_4 | 293 | 299 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 905 | 910 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 790 | 793 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 812 | 815 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 887 | 890 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 894 | 897 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 921 | 924 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 985 | 988 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 821 | 824 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 981 | 983 | PF00400 | 0.438 |
TRG_NES_CRM1_1 | 254 | 269 | PF08389 | 0.387 |
TRG_NES_CRM1_1 | 899 | 912 | PF08389 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.273 |
TRG_Pf-PMV_PEXEL_1 | 873 | 878 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 908 | 912 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M4 | Leptomonas seymouri | 33% | 93% |
A0A0N0P521 | Leptomonas seymouri | 77% | 100% |
A0A0S4JES4 | Bodo saltans | 56% | 98% |
A0A0S4JKV4 | Bodo saltans | 32% | 97% |
A0A1X0NLE6 | Trypanosomatidae | 65% | 99% |
A0A1X0P5E9 | Trypanosomatidae | 33% | 94% |
A0A3R7JX82 | Trypanosoma rangeli | 67% | 100% |
A0A3S7WUP9 | Leishmania donovani | 86% | 100% |
A0A3S7X9I5 | Leishmania donovani | 33% | 95% |
A0A422P2S2 | Trypanosoma rangeli | 33% | 96% |
A4HMW2 | Leishmania braziliensis | 33% | 100% |
A4HXM7 | Leishmania infantum | 86% | 100% |
A4IBI3 | Leishmania infantum | 33% | 91% |
C9ZJ61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
C9ZZ57 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 98% |
E9AFB9 | Leishmania major | 34% | 100% |
E9ARD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B6H4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 95% |
O04647 | Arabidopsis thaliana | 21% | 97% |
Q4QE41 | Leishmania major | 85% | 100% |
Q76C99 | Oryza sativa subsp. indica | 20% | 100% |
Q9LVQ5 | Arabidopsis thaliana | 20% | 91% |
Q9LYZ9 | Arabidopsis thaliana | 20% | 100% |
Q9SFV9 | Arabidopsis thaliana | 20% | 100% |
Q9SZ52 | Arabidopsis thaliana | 21% | 90% |
V5B5M6 | Trypanosoma cruzi | 66% | 100% |
V5BY63 | Trypanosoma cruzi | 33% | 96% |