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: A4HB27
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 | 0.297 |
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 547 | 551 | PF00656 | 0.690 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.284 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 706 | 708 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.166 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.571 |
CLV_Separin_Metazoa | 497 | 501 | PF03568 | 0.392 |
DEG_APCC_DBOX_1 | 154 | 162 | PF00400 | 0.457 |
DEG_ODPH_VHL_1 | 297 | 309 | PF01847 | 0.469 |
DOC_CKS1_1 | 171 | 176 | PF01111 | 0.510 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 245 | 254 | PF00134 | 0.550 |
DOC_CYCLIN_RxL_1 | 393 | 403 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 165 | 171 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 417 | 426 | PF00069 | 0.280 |
DOC_MAPK_MEF2A_6 | 417 | 426 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 510 | 519 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.445 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.433 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.609 |
DOC_USP7_MATH_2 | 148 | 154 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.285 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.704 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 371 | 380 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.342 |
LIG_APCC_ABBA_1 | 413 | 418 | PF00400 | 0.430 |
LIG_BIR_III_4 | 188 | 192 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 315 | 324 | PF00928 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 559 | 562 | PF00928 | 0.639 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.479 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.316 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.435 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.420 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.527 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.515 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.581 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.399 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.501 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.456 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.486 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.457 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 352 | 359 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 609 | 618 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.612 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.445 |
LIG_PCNA_yPIPBox_3 | 303 | 314 | PF02747 | 0.506 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.366 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.313 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.425 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 345 | 349 | PF00017 | 0.514 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.446 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.623 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.554 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.468 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.292 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.669 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.600 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.593 |
LIG_SH3_3 | 697 | 703 | PF00018 | 0.653 |
LIG_SH3_5 | 35 | 39 | PF00018 | 0.332 |
LIG_SUMO_SIM_anti_2 | 511 | 518 | PF11976 | 0.543 |
LIG_SUMO_SIM_anti_2 | 54 | 64 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 482 | 489 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 54 | 64 | PF11976 | 0.338 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.325 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.531 |
LIG_TRAF2_1 | 679 | 682 | PF00917 | 0.608 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.379 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.669 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.652 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.637 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.331 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.281 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.523 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.459 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.445 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.642 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.660 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.541 |
MOD_Cter_Amidation | 718 | 721 | PF01082 | 0.631 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.665 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.416 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.521 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.460 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.350 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.502 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.144 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.644 |
MOD_GlcNHglycan | 598 | 602 | PF01048 | 0.591 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.711 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.658 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.653 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.346 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.438 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.462 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.360 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.499 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.642 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.597 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.530 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.676 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.706 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.766 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.490 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.229 |
MOD_LATS_1 | 51 | 57 | PF00433 | 0.316 |
MOD_N-GLC_2 | 666 | 668 | PF02516 | 0.489 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.569 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.442 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.475 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.443 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.407 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.445 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.570 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.471 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.640 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.605 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.469 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.543 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.657 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.587 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.408 |
MOD_PK_1 | 707 | 713 | PF00069 | 0.627 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.334 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.501 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.527 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.366 |
MOD_PKB_1 | 369 | 377 | PF00069 | 0.550 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.298 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.520 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.405 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.618 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.740 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.269 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.250 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.425 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.506 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.308 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.561 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.464 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.431 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.435 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 556 | 559 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 653 | 659 | PF00179 | 0.560 |
TRG_DiLeu_BaEn_1 | 598 | 603 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.366 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.334 |
TRG_NLS_Bipartite_1 | 706 | 725 | PF00514 | 0.705 |
TRG_NLS_MonoCore_2 | 71 | 76 | PF00514 | 0.382 |
TRG_NLS_MonoExtC_3 | 719 | 724 | PF00514 | 0.505 |
TRG_NLS_MonoExtN_4 | 71 | 76 | PF00514 | 0.354 |
TRG_NLS_MonoExtN_4 | 720 | 725 | PF00514 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 120 | 125 | PF00026 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 318 | 323 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 371 | 376 | PF00026 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2R9 | Leptomonas seymouri | 69% | 100% |
A0A0S4JND8 | Bodo saltans | 44% | 99% |
A0A1X0P9Z3 | Trypanosomatidae | 54% | 100% |
A0A381MTM9 | Leishmania infantum | 79% | 99% |
A0A3R7LLL0 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X869 | Leishmania donovani | 79% | 99% |
C9ZM21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B597 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
P56960 | Mus musculus | 33% | 83% |
Q01780 | Homo sapiens | 33% | 83% |
Q12149 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q4Q2N6 | Leishmania major | 79% | 100% |
V5BQF7 | Trypanosoma cruzi | 52% | 100% |