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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000178 | exosome (RNase complex) | 4 | 2 |
GO:0000932 | P-body | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0035770 | ribonucleoprotein granule | 3 | 2 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 2 |
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:0099080 | supramolecular complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905354 | exoribonuclease complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q8M6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 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:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
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 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 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: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:0046483 | heterocycle metabolic process | 3 | 2 |
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:0071704 | organic substance metabolic process | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 2 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004527 | exonuclease activity | 5 | 4 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
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:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 842 | 844 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 853 | 855 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 928 | 930 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 853 | 855 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 928 | 930 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 754 | 756 | PF00082 | 0.386 |
CLV_PCSK_PC7_1 | 924 | 930 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 834 | 838 | PF00082 | 0.452 |
DOC_ANK_TNKS_1 | 853 | 860 | PF00023 | 0.705 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.515 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.545 |
DOC_CKS1_1 | 680 | 685 | PF01111 | 0.379 |
DOC_CYCLIN_RxL_1 | 706 | 717 | PF00134 | 0.390 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.419 |
DOC_MAPK_DCC_7 | 168 | 176 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 168 | 176 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 44 | 54 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 651 | 658 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 660 | 668 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 801 | 809 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 908 | 918 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 168 | 176 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 660 | 668 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 908 | 916 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 545 | 552 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.628 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.365 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 646 | 649 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.711 |
DOC_USP7_UBL2_3 | 844 | 848 | PF12436 | 0.660 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.375 |
LIG_14-3-3_CanoR_1 | 366 | 374 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 489 | 494 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 573 | 582 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 869 | 874 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 911 | 915 | PF00244 | 0.523 |
LIG_Actin_WH2_2 | 298 | 313 | PF00022 | 0.488 |
LIG_Actin_WH2_2 | 481 | 496 | PF00022 | 0.495 |
LIG_APCC_ABBA_1 | 893 | 898 | PF00400 | 0.459 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.430 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.471 |
LIG_EH1_1 | 606 | 614 | PF00400 | 0.509 |
LIG_EVH1_2 | 517 | 521 | PF00568 | 0.509 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.560 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.497 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.285 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.471 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.478 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.444 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.426 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.341 |
LIG_FHA_1 | 767 | 773 | PF00498 | 0.434 |
LIG_FHA_1 | 808 | 814 | PF00498 | 0.652 |
LIG_FHA_1 | 895 | 901 | PF00498 | 0.360 |
LIG_FHA_1 | 934 | 940 | PF00498 | 0.565 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.596 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.442 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.438 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.509 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.500 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.322 |
LIG_FHA_2 | 820 | 826 | PF00498 | 0.679 |
LIG_FHA_2 | 883 | 889 | PF00498 | 0.479 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.638 |
LIG_GBD_Chelix_1 | 664 | 672 | PF00786 | 0.343 |
LIG_LIR_Apic_2 | 149 | 154 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 293 | 297 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 351 | 356 | PF02991 | 0.418 |
LIG_LIR_Apic_2 | 644 | 649 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 386 | 394 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 534 | 544 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 604 | 613 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 890 | 901 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 890 | 896 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 897 | 902 | PF02991 | 0.445 |
LIG_LYPXL_S_1 | 204 | 208 | PF13949 | 0.401 |
LIG_LYPXL_SIV_4 | 438 | 446 | PF13949 | 0.471 |
LIG_LYPXL_yS_3 | 205 | 208 | PF13949 | 0.399 |
LIG_PCNA_yPIPBox_3 | 530 | 543 | PF02747 | 0.424 |
LIG_Pex14_1 | 642 | 646 | PF04695 | 0.428 |
LIG_Pex14_2 | 401 | 405 | PF04695 | 0.415 |
LIG_Pex14_3 | 532 | 537 | PF04695 | 0.428 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.428 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.434 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.515 |
LIG_SH2_CRK | 804 | 808 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 767 | 771 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 615 | 619 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 743 | 747 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 783 | 787 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 643 | 646 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.460 |
LIG_SH3_1 | 376 | 382 | PF00018 | 0.446 |
LIG_SH3_1 | 560 | 566 | PF00018 | 0.509 |
LIG_SH3_1 | 757 | 763 | PF00018 | 0.481 |
LIG_SH3_1 | 929 | 935 | PF00018 | 0.442 |
LIG_SH3_2 | 379 | 384 | PF14604 | 0.428 |
LIG_SH3_2 | 563 | 568 | PF14604 | 0.509 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.481 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.536 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.428 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.474 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.476 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.509 |
LIG_SH3_3 | 677 | 683 | PF00018 | 0.532 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.483 |
LIG_SH3_3 | 929 | 935 | PF00018 | 0.575 |
LIG_Sin3_3 | 70 | 77 | PF02671 | 0.344 |
LIG_SUMO_SIM_anti_2 | 768 | 774 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 897 | 904 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 312 | 320 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 901 | 907 | PF11976 | 0.357 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.580 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.365 |
LIG_TRAF2_1 | 587 | 590 | PF00917 | 0.476 |
LIG_TRAF2_1 | 818 | 821 | PF00917 | 0.667 |
LIG_TRAF2_1 | 885 | 888 | PF00917 | 0.516 |
LIG_TYR_ITIM | 552 | 557 | PF00017 | 0.279 |
LIG_UBA3_1 | 481 | 487 | PF00899 | 0.253 |
LIG_UBA3_1 | 749 | 757 | PF00899 | 0.461 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.460 |
LIG_WRPW_2 | 198 | 201 | PF00400 | 0.383 |
MOD_CDC14_SPxK_1 | 648 | 651 | PF00782 | 0.252 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.427 |
MOD_CDK_SPxK_1 | 645 | 651 | PF00069 | 0.252 |
MOD_CDK_SPxxK_3 | 182 | 189 | PF00069 | 0.338 |
MOD_CDK_SPxxK_3 | 645 | 652 | PF00069 | 0.252 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.379 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.413 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.270 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.321 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.665 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.551 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.629 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.450 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.512 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.337 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.354 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.327 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.450 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.483 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.431 |
MOD_CK2_1 | 934 | 940 | PF00069 | 0.537 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.715 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.370 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.568 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.367 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.306 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.529 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.362 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.494 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.298 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.479 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.661 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.681 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.611 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.450 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.482 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.513 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.383 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.383 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.170 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.455 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.290 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.255 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.488 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.677 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.719 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.603 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.459 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.378 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.383 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.418 |
MOD_N-GLC_1 | 795 | 800 | PF02516 | 0.568 |
MOD_N-GLC_2 | 727 | 729 | PF02516 | 0.481 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.252 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.483 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.252 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.313 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.451 |
MOD_NEK2_1 | 766 | 771 | PF00069 | 0.498 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.477 |
MOD_NEK2_1 | 903 | 908 | PF00069 | 0.503 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.459 |
MOD_PKA_1 | 853 | 859 | PF00069 | 0.576 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.448 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.275 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.237 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.516 |
MOD_PKA_2 | 853 | 859 | PF00069 | 0.634 |
MOD_PKA_2 | 910 | 916 | PF00069 | 0.533 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.567 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.526 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.567 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.252 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.122 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.433 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.248 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.322 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.437 |
MOD_Plk_2-3 | 416 | 422 | PF00069 | 0.183 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.327 |
MOD_Plk_2-3 | 786 | 792 | PF00069 | 0.450 |
MOD_Plk_2-3 | 94 | 100 | PF00069 | 0.602 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.507 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.369 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.405 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.368 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.488 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.252 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.276 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.279 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.383 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.402 |
MOD_Plk_4 | 776 | 782 | PF00069 | 0.466 |
MOD_Plk_4 | 786 | 792 | PF00069 | 0.516 |
MOD_Plk_4 | 869 | 875 | PF00069 | 0.495 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.533 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.472 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.348 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.538 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.440 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.259 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.375 |
MOD_SUMO_rev_2 | 391 | 400 | PF00179 | 0.330 |
MOD_SUMO_rev_2 | 812 | 818 | PF00179 | 0.653 |
TRG_AP2beta_CARGO_1 | 534 | 543 | PF09066 | 0.252 |
TRG_DiLeu_BaEn_1 | 534 | 539 | PF01217 | 0.275 |
TRG_DiLeu_BaEn_1 | 777 | 782 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_1 | 898 | 903 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_4 | 534 | 540 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 804 | 807 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 558 | 560 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 569 | 571 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 650 | 652 | PF00400 | 0.252 |
TRG_ER_diArg_1 | 852 | 854 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 928 | 930 | PF00400 | 0.471 |
TRG_NES_CRM1_1 | 764 | 777 | PF08389 | 0.365 |
TRG_NES_CRM1_1 | 894 | 909 | PF08389 | 0.409 |
TRG_NLS_MonoExtC_3 | 470 | 475 | PF00514 | 0.255 |
TRG_NLS_MonoExtN_4 | 471 | 476 | PF00514 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.252 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ70 | Leptomonas seymouri | 60% | 99% |
A0A0S4KIX9 | Bodo saltans | 37% | 100% |
A0A1X0NYL5 | Trypanosomatidae | 41% | 97% |
A0A3Q8IHX8 | Leishmania donovani | 95% | 100% |
A0A422P1Q3 | Trypanosoma rangeli | 40% | 100% |
A0JN80 | Bos taurus | 28% | 89% |
A4HG84 | Leishmania braziliensis | 80% | 100% |
A4I3A3 | Leishmania infantum | 95% | 100% |
D0A7T6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
D0A826 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AZK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P0DM58 | Arabidopsis thaliana | 32% | 89% |
Q08162 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q0P4R5 | Xenopus tropicalis | 27% | 91% |
Q0V9R3 | Xenopus tropicalis | 30% | 100% |
Q0WPN0 | Arabidopsis thaliana | 32% | 89% |
Q5R5N8 | Pongo abelii | 28% | 89% |
Q5U2P0 | Rattus norvegicus | 27% | 89% |
Q8C0S1 | Mus musculus | 28% | 89% |
Q8CI75 | Mus musculus | 30% | 100% |
Q8TF46 | Homo sapiens | 27% | 89% |
Q9CSH3 | Mus musculus | 28% | 98% |
Q9Y2L1 | Homo sapiens | 27% | 98% |