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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q2X8
Term | Name | Level | Count |
---|---|---|---|
GO:0000288 | nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay | 6 | 2 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 6 | 2 |
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009896 | positive regulation of catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0017148 | negative regulation of translation | 7 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0034249 | negative regulation of amide metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043487 | regulation of RNA stability | 3 | 2 |
GO:0043488 | regulation of mRNA stability | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
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:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050779 | RNA destabilization | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0051248 | negative regulation of protein metabolic process | 6 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 2 |
GO:0061014 | positive regulation of mRNA catabolic process | 7 | 2 |
GO:0061157 | mRNA destabilization | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 2 |
GO:1903313 | positive regulation of mRNA metabolic process | 7 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
GO:2000113 | obsolete negative regulation of cellular macromolecule biosynthetic process | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 3 |
GO:0004527 | exonuclease activity | 5 | 3 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 2 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:0004519 | endonuclease activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 406 | 412 | PF00089 | 0.361 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.218 |
CLV_PCSK_FUR_1 | 494 | 498 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 571 | 573 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 567 | 573 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.576 |
CLV_Separin_Metazoa | 665 | 669 | PF03568 | 0.425 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.604 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.394 |
DOC_MAPK_MEF2A_6 | 239 | 247 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 60 | 69 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 140 | 146 | PF00149 | 0.423 |
DOC_PP1_RVXF_1 | 64 | 70 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.558 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.566 |
DOC_PP2B_LxvP_1 | 639 | 642 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.555 |
DOC_PP4_FxxP_1 | 682 | 685 | PF00568 | 0.425 |
DOC_PP4_FxxP_1 | 69 | 72 | PF00568 | 0.583 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.686 |
DOC_USP7_UBL2_3 | 571 | 575 | PF12436 | 0.374 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 515 | 522 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 99 | 106 | PF00244 | 0.607 |
LIG_Actin_WH2_2 | 403 | 419 | PF00022 | 0.365 |
LIG_APCC_ABBA_1 | 8 | 13 | PF00400 | 0.585 |
LIG_APCC_ABBAyCdc20_2 | 84 | 90 | PF00400 | 0.615 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.466 |
LIG_eIF4E_1 | 545 | 551 | PF01652 | 0.335 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.588 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.437 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.418 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.536 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.221 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.281 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.660 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.389 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.310 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.529 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.375 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.270 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.343 |
LIG_GBD_Chelix_1 | 696 | 704 | PF00786 | 0.304 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.311 |
LIG_LIR_Apic_2 | 349 | 353 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 679 | 685 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 251 | 262 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 289 | 297 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 381 | 392 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 640 | 650 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 655 | 664 | PF02991 | 0.219 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.181 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 647 | 653 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 655 | 659 | PF02991 | 0.271 |
LIG_NRBOX | 549 | 555 | PF00104 | 0.419 |
LIG_PCNA_yPIPBox_3 | 149 | 161 | PF02747 | 0.439 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.396 |
LIG_Pex14_2 | 646 | 650 | PF04695 | 0.425 |
LIG_PTB_Apo_2 | 138 | 145 | PF02174 | 0.365 |
LIG_PTB_Apo_2 | 683 | 690 | PF02174 | 0.320 |
LIG_PTB_Phospho_1 | 683 | 689 | PF10480 | 0.320 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.423 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.304 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.389 |
LIG_SH2_CRK | 463 | 467 | PF00017 | 0.320 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 177 | 180 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 624 | 627 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.349 |
LIG_SH3_1 | 492 | 498 | PF00018 | 0.335 |
LIG_SH3_2 | 36 | 41 | PF14604 | 0.702 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.525 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.405 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.353 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.257 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.482 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.358 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.741 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.419 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.335 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.420 |
LIG_SH3_3 | 667 | 673 | PF00018 | 0.314 |
LIG_SH3_CIN85_PxpxPR_1 | 267 | 272 | PF14604 | 0.489 |
LIG_SUMO_SIM_anti_2 | 155 | 162 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 186 | 191 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 548 | 555 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 660 | 669 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 691 | 699 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 15 | 21 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.548 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.575 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.471 |
LIG_TYR_ITIM | 288 | 293 | PF00017 | 0.320 |
LIG_UBA3_1 | 315 | 322 | PF00899 | 0.372 |
LIG_WW_3 | 70 | 74 | PF00397 | 0.620 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.520 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.425 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.567 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.342 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.396 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.401 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.375 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.707 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.573 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.410 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.339 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.411 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.344 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.343 |
MOD_CK2_1 | 671 | 677 | PF00069 | 0.413 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.635 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.677 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.368 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.381 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.334 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.615 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.464 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.582 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.374 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.460 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.511 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.434 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.394 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.643 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.394 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.388 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.515 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.390 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.423 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.673 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.496 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.389 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.304 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.468 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.339 |
MOD_N-GLC_2 | 453 | 455 | PF02516 | 0.304 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.565 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.379 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.320 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.408 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.460 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.322 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.311 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.397 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.456 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.600 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.438 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.401 |
MOD_PK_1 | 367 | 373 | PF00069 | 0.425 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.673 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.538 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.496 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.358 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.658 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.449 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.701 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.365 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.535 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.538 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.437 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.469 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.460 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.468 |
MOD_Plk_1 | 637 | 643 | PF00069 | 0.347 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.289 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.339 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.374 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.489 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.400 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.396 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.485 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.346 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.408 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.451 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.521 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.392 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.420 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.350 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.427 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.414 |
MOD_SUMO_rev_2 | 47 | 57 | PF00179 | 0.598 |
TRG_DiLeu_BaEn_2 | 372 | 378 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_4 | 108 | 114 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 512 | 517 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 538 | 543 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.474 |
TRG_NES_CRM1_1 | 328 | 341 | PF08389 | 0.257 |
TRG_NES_CRM1_1 | 662 | 675 | PF08389 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 541 | 546 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC26 | Leptomonas seymouri | 62% | 99% |
A0A0S4J452 | Bodo saltans | 32% | 100% |
A0A1X0PAG3 | Trypanosomatidae | 44% | 100% |
A0A3R7LBT2 | Trypanosoma rangeli | 42% | 100% |
A0A3S7X813 | Leishmania donovani | 94% | 100% |
A4HAT4 | Leishmania braziliensis | 80% | 83% |
A4I9Z4 | Leishmania infantum | 94% | 85% |
C9ZMN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B508 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q3TIU4 | Mus musculus | 25% | 100% |
Q6AXQ5 | Rattus norvegicus | 25% | 100% |
Q8W0Z9 | Arabidopsis thaliana | 24% | 100% |
V5DGT6 | Trypanosoma cruzi | 42% | 100% |