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:0000176 | nuclear exosome (RNase complex) | 3 | 12 |
GO:0000178 | exosome (RNase complex) | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1905354 | exoribonuclease complex | 3 | 12 |
GO:0005730 | nucleolus | 5 | 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: A0A3S7X869
Term | Name | Level | Count |
---|---|---|---|
GO:0000459 | exonucleolytic trimming involved in rRNA processing | 8 | 12 |
GO:0000467 | exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 12 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0031125 | rRNA 3'-end processing | 9 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 12 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 12 |
GO:0090503 | RNA phosphodiester bond hydrolysis, exonucleolytic | 7 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006402 | mRNA catabolic process | 6 | 1 |
GO:0008334 | histone mRNA metabolic process | 7 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016073 | snRNA metabolic process | 7 | 1 |
GO:0016074 | sno(s)RNA metabolic process | 7 | 1 |
GO:0016075 | rRNA catabolic process | 7 | 1 |
GO:0016076 | snRNA catabolic process | 7 | 1 |
GO:0016077 | sno(s)RNA catabolic process | 7 | 1 |
GO:0016078 | tRNA catabolic process | 7 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0031126 | sno(s)RNA 3'-end processing | 9 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0034661 | ncRNA catabolic process | 6 | 1 |
GO:0042868 | antisense RNA metabolic process | 7 | 1 |
GO:0043144 | sno(s)RNA processing | 8 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0043633 | polyadenylation-dependent RNA catabolic process | 6 | 1 |
GO:0043634 | polyadenylation-dependent ncRNA catabolic process | 7 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071025 | RNA surveillance | 6 | 1 |
GO:0071027 | nuclear RNA surveillance | 7 | 1 |
GO:0071029 | nuclear ncRNA surveillance | 7 | 1 |
GO:0071034 | CUT catabolic process | 7 | 1 |
GO:0071035 | nuclear polyadenylation-dependent rRNA catabolic process | 8 | 1 |
GO:0071036 | nuclear polyadenylation-dependent snoRNA catabolic process | 8 | 1 |
GO:0071037 | nuclear polyadenylation-dependent snRNA catabolic process | 8 | 1 |
GO:0071038 | nuclear polyadenylation-dependent tRNA catabolic process | 8 | 1 |
GO:0071039 | nuclear polyadenylation-dependent CUT catabolic process | 8 | 1 |
GO:0071040 | nuclear polyadenylation-dependent antisense transcript catabolic process | 8 | 1 |
GO:0071041 | antisense RNA transcript catabolic process | 7 | 1 |
GO:0071043 | CUT metabolic process | 7 | 1 |
GO:0071044 | histone mRNA catabolic process | 8 | 1 |
GO:0071046 | nuclear polyadenylation-dependent ncRNA catabolic process | 8 | 1 |
GO:0071051 | polyadenylation-dependent snoRNA 3'-end processing | 10 | 1 |
GO:0106354 | tRNA surveillance | 7 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 12 |
GO:0004527 | exonuclease activity | 5 | 12 |
GO:0004532 | RNA exonuclease activity | 5 | 12 |
GO:0004540 | RNA nuclease activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 12 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003727 | single-stranded RNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.295 |
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.295 |
CLV_C14_Caspase3-7 | 691 | 695 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.164 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.681 |
DEG_ODPH_VHL_1 | 297 | 309 | PF01847 | 0.467 |
DEG_SIAH_1 | 218 | 226 | PF03145 | 0.522 |
DOC_CKS1_1 | 171 | 176 | PF01111 | 0.495 |
DOC_CKS1_1 | 2 | 7 | PF01111 | 0.685 |
DOC_CYCLIN_RxL_1 | 245 | 254 | PF00134 | 0.548 |
DOC_CYCLIN_RxL_1 | 393 | 403 | PF00134 | 0.442 |
DOC_MAPK_DCC_7 | 220 | 228 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 165 | 171 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 14 | 21 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 220 | 228 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 510 | 519 | PF00069 | 0.544 |
DOC_PP1_SILK_1 | 304 | 309 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.443 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.630 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.283 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.454 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 728 | 732 | PF12436 | 0.701 |
DOC_USP7_UBL2_3 | 738 | 742 | PF12436 | 0.716 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 291 | 295 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 371 | 380 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 551 | 560 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 675 | 680 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.407 |
LIG_APCC_ABBA_1 | 413 | 418 | PF00400 | 0.430 |
LIG_APCC_ABBAyCdc20_2 | 49 | 55 | PF00400 | 0.240 |
LIG_BIR_III_2 | 229 | 233 | PF00653 | 0.460 |
LIG_BIR_III_4 | 188 | 192 | PF00653 | 0.521 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.570 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.559 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 315 | 324 | PF00928 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 559 | 562 | PF00928 | 0.672 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.489 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.443 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.421 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.525 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.513 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.593 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.414 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.484 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.315 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.454 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.689 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.657 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.395 |
LIG_GBD_Chelix_1 | 251 | 259 | PF00786 | 0.204 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 352 | 359 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 609 | 618 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.637 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.443 |
LIG_PCNA_yPIPBox_3 | 303 | 314 | PF02747 | 0.504 |
LIG_RPA_C_Fungi | 150 | 162 | PF08784 | 0.526 |
LIG_RPA_C_Fungi | 636 | 648 | PF08784 | 0.562 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.311 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.268 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.674 |
LIG_SH2_NCK_1 | 427 | 431 | PF00017 | 0.406 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.311 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.291 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.496 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.516 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.457 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.617 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.576 |
LIG_SH3_5 | 35 | 39 | PF00018 | 0.330 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 511 | 518 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 54 | 64 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 482 | 489 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 54 | 64 | PF11976 | 0.336 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.415 |
LIG_TRAF2_1 | 595 | 598 | PF00917 | 0.682 |
LIG_TRAF2_1 | 661 | 664 | PF00917 | 0.709 |
LIG_TRAF2_2 | 626 | 631 | PF00917 | 0.533 |
LIG_UBA3_1 | 515 | 521 | PF00899 | 0.407 |
LIG_UBA3_1 | 709 | 714 | PF00899 | 0.642 |
LIG_Vh1_VBS_1 | 99 | 117 | PF01044 | 0.289 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.369 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.525 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.388 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.490 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.375 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.741 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.658 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.726 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.279 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.429 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.315 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.669 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.706 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.674 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.677 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.326 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.539 |
MOD_Cter_Amidation | 736 | 739 | PF01082 | 0.661 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.641 |
MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.458 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.496 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.423 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.443 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.530 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.154 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.495 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.578 |
MOD_GlcNHglycan | 597 | 602 | PF01048 | 0.648 |
MOD_GlcNHglycan | 666 | 670 | PF01048 | 0.737 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.396 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.344 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.278 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.533 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.436 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.351 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.310 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.581 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.712 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.639 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.527 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.723 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.774 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.409 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.341 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.570 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.564 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.364 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.295 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.295 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.295 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.420 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.295 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.570 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.610 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.483 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.669 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.658 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.330 |
MOD_NEK2_2 | 715 | 720 | PF00069 | 0.674 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.518 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.541 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.722 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.406 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.654 |
MOD_PK_1 | 208 | 214 | PF00069 | 0.463 |
MOD_PK_1 | 675 | 681 | PF00069 | 0.649 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.332 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.333 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.447 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.374 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.379 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.407 |
MOD_PKB_1 | 369 | 377 | PF00069 | 0.443 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.347 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.397 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.402 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.662 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.369 |
MOD_Plk_2-3 | 543 | 549 | PF00069 | 0.492 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.369 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.267 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.248 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.514 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.535 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.408 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.350 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.497 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.339 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.380 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.316 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.713 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.325 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.691 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.444 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.295 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.651 |
MOD_SUMO_for_1 | 719 | 722 | PF00179 | 0.629 |
TRG_DiLeu_BaEn_1 | 598 | 603 | PF01217 | 0.692 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.649 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.332 |
TRG_NLS_MonoCore_2 | 71 | 76 | PF00514 | 0.380 |
TRG_NLS_MonoExtN_4 | 71 | 76 | PF00514 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 120 | 125 | PF00026 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 318 | 323 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 371 | 376 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2R9 | Leptomonas seymouri | 69% | 100% |
A0A0S4JND8 | Bodo saltans | 48% | 100% |
A0A1X0P9Z3 | Trypanosomatidae | 53% | 100% |
A0A381MTM9 | Leishmania infantum | 100% | 100% |
A0A3R7LLL0 | Trypanosoma rangeli | 55% | 100% |
A4HB27 | Leishmania braziliensis | 79% | 100% |
C9ZM21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B597 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P56960 | Mus musculus | 34% | 84% |
Q01780 | Homo sapiens | 33% | 84% |
Q4Q2N6 | Leishmania major | 93% | 100% |
V5BQF7 | Trypanosoma cruzi | 52% | 100% |