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: A4I9Z4
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 | 23 | 27 | PF00656 | 0.574 |
CLV_MEL_PAP_1 | 533 | 539 | PF00089 | 0.340 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 621 | 625 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.735 |
CLV_PCSK_PC1ET2_1 | 698 | 700 | PF00082 | 0.405 |
CLV_PCSK_PC7_1 | 121 | 127 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 619 | 625 | PF00082 | 0.313 |
CLV_PCSK_PC7_1 | 694 | 700 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 683 | 687 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.349 |
CLV_Separin_Metazoa | 792 | 796 | PF03568 | 0.421 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.573 |
DEG_SCF_FBW7_1 | 91 | 98 | PF00400 | 0.503 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.738 |
DOC_CYCLIN_RxL_1 | 118 | 127 | PF00134 | 0.483 |
DOC_MAPK_MEF2A_6 | 187 | 196 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 366 | 374 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 191 | 197 | PF00149 | 0.474 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 658 | 664 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 766 | 769 | PF13499 | 0.458 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.573 |
DOC_PP4_FxxP_1 | 809 | 812 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.728 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 53 | 57 | PF12436 | 0.602 |
DOC_USP7_UBL2_3 | 698 | 702 | PF12436 | 0.313 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 18 | 25 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 226 | 233 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 371 | 375 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 642 | 649 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 701 | 710 | PF00244 | 0.274 |
LIG_Actin_WH2_2 | 546 | 562 | PF00022 | 0.223 |
LIG_APCC_ABBA_1 | 135 | 140 | PF00400 | 0.470 |
LIG_APCC_ABBAyCdc20_2 | 211 | 217 | PF00400 | 0.513 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 526 | 530 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.584 |
LIG_eIF4E_1 | 672 | 678 | PF01652 | 0.287 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.729 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.570 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.551 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.423 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.410 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.295 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.259 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.345 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.398 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.286 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.504 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.570 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.374 |
LIG_FHA_2 | 709 | 715 | PF00498 | 0.356 |
LIG_FHA_2 | 774 | 780 | PF00498 | 0.319 |
LIG_LIR_Apic_2 | 476 | 480 | PF02991 | 0.405 |
LIG_LIR_Apic_2 | 806 | 812 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 256 | 267 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 378 | 389 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 416 | 424 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 508 | 519 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 767 | 777 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 782 | 791 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 527 | 533 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 638 | 644 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 767 | 773 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 774 | 780 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 782 | 786 | PF02991 | 0.287 |
LIG_NRBOX | 676 | 682 | PF00104 | 0.414 |
LIG_PCNA_yPIPBox_3 | 276 | 288 | PF02747 | 0.362 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.382 |
LIG_Pex14_2 | 773 | 777 | PF04695 | 0.421 |
LIG_PTB_Apo_2 | 265 | 272 | PF02174 | 0.325 |
LIG_PTB_Apo_2 | 810 | 817 | PF02174 | 0.295 |
LIG_PTB_Phospho_1 | 810 | 816 | PF10480 | 0.295 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.358 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.280 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.374 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.295 |
LIG_SH2_CRK | 641 | 645 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 304 | 307 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.295 |
LIG_SH2_STAT3 | 751 | 754 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 783 | 786 | PF00017 | 0.327 |
LIG_SH3_1 | 619 | 625 | PF00018 | 0.287 |
LIG_SH3_2 | 163 | 168 | PF14604 | 0.649 |
LIG_SH3_2 | 264 | 269 | PF14604 | 0.281 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.371 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.285 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.773 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.448 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.380 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.360 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.494 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.341 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.414 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.305 |
LIG_SH3_3 | 794 | 800 | PF00018 | 0.297 |
LIG_SH3_CIN85_PxpxPR_1 | 394 | 399 | PF14604 | 0.427 |
LIG_SUMO_SIM_anti_2 | 313 | 318 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 675 | 682 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 787 | 796 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 818 | 826 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 439 | 446 | PF11976 | 0.285 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.552 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.462 |
LIG_TYR_ITIM | 415 | 420 | PF00017 | 0.295 |
LIG_UBA3_1 | 442 | 449 | PF00899 | 0.351 |
LIG_WW_3 | 197 | 201 | PF00397 | 0.612 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.501 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.683 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.791 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.564 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.532 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.443 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.551 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.318 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.382 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.402 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.737 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.355 |
MOD_CK1_1 | 723 | 729 | PF00069 | 0.389 |
MOD_CK1_1 | 787 | 793 | PF00069 | 0.380 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.645 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.719 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.500 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.432 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.315 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.419 |
MOD_CK2_1 | 773 | 779 | PF00069 | 0.321 |
MOD_CK2_1 | 798 | 804 | PF00069 | 0.405 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.729 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.596 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.641 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.686 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.353 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.428 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.660 |
MOD_GlcNHglycan | 703 | 706 | PF01048 | 0.329 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.667 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.589 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.410 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.635 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.498 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.447 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.601 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.627 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.533 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.417 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.662 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.386 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.495 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.390 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.398 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.762 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.397 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.438 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.750 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.474 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.374 |
MOD_N-GLC_1 | 632 | 637 | PF02516 | 0.280 |
MOD_N-GLC_1 | 723 | 728 | PF02516 | 0.491 |
MOD_N-GLC_1 | 771 | 776 | PF02516 | 0.315 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.427 |
MOD_N-GLC_2 | 580 | 582 | PF02516 | 0.280 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.614 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.530 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.496 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.329 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.376 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.477 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.313 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.295 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.400 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.457 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.484 |
MOD_PIKK_1 | 723 | 729 | PF00454 | 0.441 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.541 |
MOD_PK_1 | 385 | 391 | PF00069 | 0.336 |
MOD_PK_1 | 494 | 500 | PF00069 | 0.421 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.678 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.546 |
MOD_PKA_1 | 701 | 707 | PF00069 | 0.396 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.489 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.655 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.484 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.605 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.539 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.493 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.341 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.458 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.281 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.720 |
MOD_PKB_1 | 699 | 707 | PF00069 | 0.223 |
MOD_PKB_1 | 9 | 17 | PF00069 | 0.474 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.448 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.631 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.435 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.399 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.465 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.586 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.488 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.357 |
MOD_Plk_1 | 771 | 777 | PF00069 | 0.298 |
MOD_Plk_1 | 787 | 793 | PF00069 | 0.315 |
MOD_Plk_2-3 | 561 | 567 | PF00069 | 0.300 |
MOD_Plk_2-3 | 652 | 658 | PF00069 | 0.313 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.418 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.360 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.382 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.476 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.336 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.528 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.322 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.461 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.407 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.514 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.531 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.379 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.659 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.542 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.506 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.365 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.298 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.432 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 174 | 184 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 679 | 688 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_2 | 499 | 505 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 119 | 124 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 639 | 644 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 665 | 670 | PF01217 | 0.374 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 783 | 786 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 619 | 622 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 623 | 625 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.686 |
TRG_NES_CRM1_1 | 789 | 802 | PF08389 | 0.365 |
TRG_NLS_MonoCore_2 | 697 | 702 | PF00514 | 0.345 |
TRG_NLS_MonoExtC_3 | 697 | 702 | PF00514 | 0.223 |
TRG_NLS_MonoExtN_4 | 695 | 702 | PF00514 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 668 | 673 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC26 | Leptomonas seymouri | 62% | 100% |
A0A0S4J452 | Bodo saltans | 32% | 100% |
A0A1X0PAG3 | Trypanosomatidae | 43% | 100% |
A0A3R7LBT2 | Trypanosoma rangeli | 43% | 100% |
A0A3S7X813 | Leishmania donovani | 100% | 100% |
A4HAT4 | Leishmania braziliensis | 76% | 100% |
C9ZMN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B508 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q2X8 | Leishmania major | 94% | 100% |
V5DGT6 | Trypanosoma cruzi | 42% | 100% |