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: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: A4HAT4
Term | Name | Level | Count |
---|---|---|---|
GO:0000288 | nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay | 6 | 1 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006402 | mRNA catabolic process | 6 | 1 |
GO:0006417 | regulation of translation | 6 | 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:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009896 | positive regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0017148 | negative regulation of translation | 7 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0034249 | negative regulation of amide metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 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:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 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:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050779 | RNA destabilization | 4 | 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:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051248 | negative regulation of protein metabolic process | 6 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0061014 | positive regulation of mRNA catabolic process | 7 | 1 |
GO:0061157 | mRNA destabilization | 5 | 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:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903313 | positive regulation of mRNA metabolic process | 7 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
GO:2000113 | obsolete negative regulation of cellular macromolecule biosynthetic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 1 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004527 | exonuclease activity | 5 | 2 |
GO:0004532 | RNA exonuclease activity | 5 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.382 |
CLV_MEL_PAP_1 | 547 | 553 | PF00089 | 0.340 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 217 | 223 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 4 | 10 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.349 |
CLV_Separin_Metazoa | 806 | 810 | PF03568 | 0.421 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.423 |
DEG_COP1_1 | 113 | 122 | PF00400 | 0.483 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.567 |
DEG_SIAH_1 | 119 | 127 | PF03145 | 0.445 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.687 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 615 | 618 | PF00134 | 0.197 |
DOC_MAPK_gen_1 | 181 | 188 | PF00069 | 0.444 |
DOC_MAPK_HePTP_8 | 198 | 210 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 201 | 210 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 205 | 211 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 672 | 678 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.577 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 615 | 618 | PF13499 | 0.197 |
DOC_PP2B_LxvP_1 | 780 | 783 | PF13499 | 0.458 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.602 |
DOC_PP4_FxxP_1 | 823 | 826 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.645 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 385 | 389 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 656 | 663 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 544 | 560 | PF00022 | 0.337 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.536 |
LIG_APCC_ABBAyCdc20_2 | 225 | 231 | PF00400 | 0.519 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 626 | 630 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.585 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.466 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.586 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.396 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.418 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.295 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.398 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.249 |
LIG_FHA_1 | 808 | 814 | PF00498 | 0.287 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.391 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.448 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.231 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.319 |
LIG_LIR_Apic_2 | 821 | 826 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 270 | 281 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 430 | 438 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 522 | 533 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 781 | 791 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 796 | 805 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 652 | 658 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 781 | 787 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 788 | 794 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.287 |
LIG_NRBOX | 690 | 696 | PF00104 | 0.414 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.410 |
LIG_Pex14_2 | 787 | 791 | PF04695 | 0.421 |
LIG_PTB_Apo_2 | 279 | 286 | PF02174 | 0.359 |
LIG_PTB_Apo_2 | 824 | 831 | PF02174 | 0.295 |
LIG_PTB_Phospho_1 | 824 | 830 | PF10480 | 0.295 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.428 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.280 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.374 |
LIG_SH2_CRK | 604 | 608 | PF00017 | 0.295 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 303 | 307 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 318 | 321 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.293 |
LIG_SH2_STAT3 | 765 | 768 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 797 | 800 | PF00017 | 0.327 |
LIG_SH3_1 | 809 | 815 | PF00018 | 0.225 |
LIG_SH3_2 | 177 | 182 | PF14604 | 0.636 |
LIG_SH3_2 | 212 | 217 | PF14604 | 0.432 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.617 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.444 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.763 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.544 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.403 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.366 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.336 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.385 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.414 |
LIG_SH3_3 | 808 | 814 | PF00018 | 0.296 |
LIG_SH3_4 | 55 | 62 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 327 | 332 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 801 | 810 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 832 | 840 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 453 | 460 | PF11976 | 0.285 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.583 |
LIG_TYR_ITIM | 316 | 321 | PF00017 | 0.466 |
LIG_TYR_ITIM | 429 | 434 | PF00017 | 0.295 |
LIG_UBA3_1 | 127 | 135 | PF00899 | 0.423 |
LIG_WRPW_2 | 10 | 13 | PF00400 | 0.499 |
LIG_WW_3 | 211 | 215 | PF00397 | 0.632 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.744 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.641 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.557 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.558 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.458 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.318 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.382 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.792 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.378 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.700 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.389 |
MOD_CK1_1 | 801 | 807 | PF00069 | 0.380 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.704 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.507 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.424 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.315 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.419 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.321 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.689 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.669 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.568 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.563 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.566 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.563 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.353 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.197 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.651 |
MOD_GlcNHglycan | 744 | 748 | PF01048 | 0.368 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.800 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.747 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.722 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.599 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.491 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.460 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.671 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.587 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.706 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.635 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.510 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.442 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.647 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.533 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.425 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.386 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.573 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.494 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.390 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.398 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.775 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.397 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.438 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.660 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.454 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.522 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.521 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.374 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.280 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.491 |
MOD_N-GLC_1 | 785 | 790 | PF02516 | 0.315 |
MOD_N-GLC_2 | 594 | 596 | PF02516 | 0.280 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.617 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.400 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.499 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.329 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.594 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.376 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.313 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.477 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.313 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.295 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.400 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.346 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.517 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.563 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.505 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.499 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.514 |
MOD_PIKK_1 | 709 | 715 | PF00454 | 0.252 |
MOD_PIKK_1 | 737 | 743 | PF00454 | 0.441 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.580 |
MOD_PK_1 | 508 | 514 | PF00069 | 0.421 |
MOD_PKA_1 | 181 | 187 | PF00069 | 0.707 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.508 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.557 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.684 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.627 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.559 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.533 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.483 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.341 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.458 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.764 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.507 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.370 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.457 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.361 |
MOD_Plk_1 | 611 | 617 | PF00069 | 0.488 |
MOD_Plk_1 | 778 | 784 | PF00069 | 0.357 |
MOD_Plk_1 | 785 | 791 | PF00069 | 0.298 |
MOD_Plk_1 | 801 | 807 | PF00069 | 0.315 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.300 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.544 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.359 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.389 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.461 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.407 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.684 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.538 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.600 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.377 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.647 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.513 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.298 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.456 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.444 |
MOD_SUMO_rev_2 | 190 | 198 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_2 | 513 | 519 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 653 | 658 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 679 | 684 | PF01217 | 0.374 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 797 | 800 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.528 |
TRG_NES_CRM1_1 | 803 | 816 | PF08389 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 682 | 687 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC26 | Leptomonas seymouri | 62% | 100% |
A0A0S4J452 | Bodo saltans | 33% | 100% |
A0A1X0PAG3 | Trypanosomatidae | 44% | 100% |
A0A3R7LBT2 | Trypanosoma rangeli | 42% | 100% |
A0A3S7X813 | Leishmania donovani | 80% | 100% |
A4I9Z4 | Leishmania infantum | 76% | 100% |
C9ZMN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B508 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q2X8 | Leishmania major | 80% | 99% |
V5DGT6 | Trypanosoma cruzi | 42% | 100% |