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:0005730 | nucleolus | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1905354 | exoribonuclease complex | 3 | 12 |
Related structures:
AlphaFold database: Q4Q2N6
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:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008334 | histone mRNA metabolic process | 7 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0016073 | snRNA metabolic process | 7 | 2 |
GO:0016074 | sno(s)RNA metabolic process | 7 | 2 |
GO:0016075 | rRNA catabolic process | 7 | 2 |
GO:0016076 | snRNA catabolic process | 7 | 2 |
GO:0016077 | sno(s)RNA catabolic process | 7 | 2 |
GO:0016078 | tRNA catabolic process | 7 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0031125 | rRNA 3'-end processing | 9 | 12 |
GO:0031126 | sno(s)RNA 3'-end processing | 9 | 2 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0034661 | ncRNA catabolic process | 6 | 2 |
GO:0042868 | antisense RNA metabolic process | 7 | 2 |
GO:0043144 | sno(s)RNA processing | 8 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 12 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0043633 | polyadenylation-dependent RNA catabolic process | 6 | 2 |
GO:0043634 | polyadenylation-dependent ncRNA catabolic process | 7 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071025 | RNA surveillance | 6 | 2 |
GO:0071027 | nuclear RNA surveillance | 7 | 2 |
GO:0071029 | nuclear ncRNA surveillance | 7 | 2 |
GO:0071034 | CUT catabolic process | 7 | 2 |
GO:0071035 | nuclear polyadenylation-dependent rRNA catabolic process | 8 | 2 |
GO:0071036 | nuclear polyadenylation-dependent snoRNA catabolic process | 8 | 2 |
GO:0071037 | nuclear polyadenylation-dependent snRNA catabolic process | 8 | 2 |
GO:0071038 | nuclear polyadenylation-dependent tRNA catabolic process | 8 | 2 |
GO:0071039 | nuclear polyadenylation-dependent CUT catabolic process | 8 | 2 |
GO:0071040 | nuclear polyadenylation-dependent antisense transcript catabolic process | 8 | 2 |
GO:0071041 | antisense RNA transcript catabolic process | 7 | 2 |
GO:0071043 | CUT metabolic process | 7 | 2 |
GO:0071044 | histone mRNA catabolic process | 8 | 2 |
GO:0071046 | nuclear polyadenylation-dependent ncRNA catabolic process | 8 | 2 |
GO:0071051 | polyadenylation-dependent snoRNA 3'-end processing | 10 | 2 |
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:0106354 | tRNA surveillance | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
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:0003723 | RNA binding | 4 | 2 |
GO:0003727 | single-stranded RNA binding | 5 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.266 |
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.266 |
CLV_C14_Caspase3-7 | 690 | 694 | PF00656 | 0.654 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.266 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.152 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 713 | 717 | PF00082 | 0.652 |
DEG_ODPH_VHL_1 | 296 | 308 | PF01847 | 0.448 |
DEG_SIAH_1 | 217 | 225 | PF03145 | 0.495 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.474 |
DOC_CKS1_1 | 2 | 7 | PF01111 | 0.661 |
DOC_CYCLIN_RxL_1 | 244 | 253 | PF00134 | 0.508 |
DOC_CYCLIN_RxL_1 | 391 | 402 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 340 | 346 | PF00134 | 0.498 |
DOC_MAPK_DCC_7 | 219 | 227 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 164 | 170 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 14 | 21 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 219 | 227 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.538 |
DOC_PP1_SILK_1 | 303 | 308 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.422 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.391 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.583 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.386 |
DOC_USP7_UBL2_3 | 727 | 731 | PF12436 | 0.679 |
DOC_USP7_UBL2_3 | 737 | 741 | PF12436 | 0.700 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 29 | 36 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 370 | 379 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 674 | 679 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.396 |
LIG_APCC_ABBA_1 | 412 | 417 | PF00400 | 0.381 |
LIG_BIR_III_2 | 228 | 232 | PF00653 | 0.421 |
LIG_BIR_III_4 | 187 | 191 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.461 |
LIG_deltaCOP1_diTrp_1 | 314 | 323 | PF00928 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 558 | 561 | PF00928 | 0.636 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.460 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.422 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.514 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.501 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.484 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.568 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.399 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.464 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.594 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.286 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.443 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.662 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.604 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.376 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 351 | 358 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 608 | 617 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.643 |
LIG_NRBOX | 393 | 399 | PF00104 | 0.422 |
LIG_PCNA_yPIPBox_3 | 242 | 252 | PF02747 | 0.367 |
LIG_PCNA_yPIPBox_3 | 302 | 313 | PF02747 | 0.488 |
LIG_Rb_pABgroove_1 | 325 | 333 | PF01858 | 0.388 |
LIG_RPA_C_Fungi | 635 | 647 | PF08784 | 0.510 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.282 |
LIG_SH2_CRK | 562 | 566 | PF00017 | 0.672 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.382 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.282 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.282 |
LIG_SH2_STAT3 | 379 | 382 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.268 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.461 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.511 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.422 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.577 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.541 |
LIG_SH3_5 | 35 | 39 | PF00018 | 0.302 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 510 | 517 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 56 | 64 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 481 | 488 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 512 | 517 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 56 | 64 | PF11976 | 0.300 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.401 |
LIG_TRAF2_1 | 594 | 597 | PF00917 | 0.617 |
LIG_TRAF2_1 | 660 | 663 | PF00917 | 0.658 |
LIG_UBA3_1 | 514 | 520 | PF00899 | 0.390 |
LIG_UBA3_1 | 708 | 713 | PF00899 | 0.600 |
LIG_Vh1_VBS_1 | 99 | 117 | PF01044 | 0.260 |
MOD_CDC14_SPxK_1 | 139 | 142 | PF00782 | 0.468 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.462 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.326 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.368 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.427 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.351 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.652 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.624 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.713 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.263 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.302 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.630 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.661 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.631 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.648 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.301 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.507 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.487 |
MOD_GlcNHglycan | 187 | 191 | PF01048 | 0.505 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.401 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.415 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.396 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.526 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.170 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.471 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.525 |
MOD_GlcNHglycan | 596 | 601 | PF01048 | 0.585 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.700 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.623 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.377 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.316 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.250 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.512 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.426 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.329 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.281 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.529 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.664 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.583 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.473 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.689 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.716 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.529 |
MOD_LATS_1 | 51 | 57 | PF00433 | 0.280 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.331 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.311 |
MOD_N-GLC_1 | 664 | 669 | PF02516 | 0.487 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.560 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.345 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.274 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.266 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.266 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.408 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.279 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.513 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.602 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.467 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.634 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.621 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.302 |
MOD_NEK2_2 | 714 | 719 | PF00069 | 0.646 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.477 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.670 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.356 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.620 |
MOD_PK_1 | 207 | 213 | PF00069 | 0.428 |
MOD_PK_1 | 674 | 680 | PF00069 | 0.608 |
MOD_PKA_1 | 540 | 546 | PF00069 | 0.416 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.304 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.189 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.305 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.409 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.368 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.438 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.356 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.390 |
MOD_PKB_1 | 368 | 376 | PF00069 | 0.386 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.189 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.378 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.387 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.329 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.602 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.326 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.326 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.239 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.222 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.477 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.526 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.386 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.324 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.522 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.371 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.260 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.287 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.709 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.297 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.669 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.530 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.429 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.266 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.604 |
MOD_SUMO_for_1 | 718 | 721 | PF00179 | 0.600 |
TRG_DiLeu_BaEn_1 | 597 | 602 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.304 |
TRG_NLS_MonoCore_2 | 71 | 76 | PF00514 | 0.358 |
TRG_NLS_MonoExtN_4 | 71 | 76 | PF00514 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 120 | 125 | PF00026 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 317 | 322 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 370 | 375 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2R9 | Leptomonas seymouri | 70% | 100% |
A0A0S4JND8 | Bodo saltans | 48% | 100% |
A0A1X0P9Z3 | Trypanosomatidae | 54% | 100% |
A0A381MTM9 | Leishmania infantum | 93% | 100% |
A0A3R7LLL0 | Trypanosoma rangeli | 54% | 100% |
A0A3S7X869 | Leishmania donovani | 93% | 100% |
A4HB27 | Leishmania braziliensis | 79% | 100% |
C9ZM21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B597 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P56960 | Mus musculus | 32% | 84% |
Q01780 | Homo sapiens | 33% | 84% |
V5BQF7 | Trypanosoma cruzi | 52% | 100% |