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 | 1 |
GO:0000932 | P-body | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 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:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905354 | exoribonuclease complex | 3 | 1 |
Related structures:
AlphaFold database: E9AZK5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006402 | mRNA catabolic process | 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:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 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:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 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: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:0046483 | heterocycle metabolic process | 3 | 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:0071704 | organic substance metabolic process | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
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:0004540 | RNA nuclease activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
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 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 1 |
GO:0004527 | exonuclease activity | 5 | 3 |
GO:0004532 | RNA exonuclease activity | 5 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.563 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 852 | 854 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 927 | 929 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 852 | 854 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 927 | 929 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 753 | 755 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 923 | 929 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 709 | 713 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 863 | 867 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 862 | 870 | PF00400 | 0.431 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.366 |
DOC_ANK_TNKS_1 | 852 | 859 | PF00023 | 0.716 |
DOC_CKS1_1 | 240 | 245 | PF01111 | 0.472 |
DOC_CKS1_1 | 679 | 684 | PF01111 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.474 |
DOC_MAPK_DCC_7 | 167 | 175 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 44 | 54 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 650 | 657 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 659 | 667 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 800 | 808 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 907 | 917 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 659 | 667 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 907 | 915 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 501 | 507 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 544 | 551 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.660 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.374 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.487 |
DOC_PP4_FxxP_1 | 645 | 648 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.654 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.431 |
DOC_USP7_UBL2_3 | 843 | 847 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 383 | 391 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 488 | 493 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 572 | 581 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 910 | 914 | PF00244 | 0.522 |
LIG_Actin_WH2_2 | 297 | 312 | PF00022 | 0.499 |
LIG_Actin_WH2_2 | 480 | 495 | PF00022 | 0.513 |
LIG_APCC_ABBA_1 | 892 | 897 | PF00400 | 0.474 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.436 |
LIG_Clathr_ClatBox_1 | 403 | 407 | PF01394 | 0.487 |
LIG_EH1_1 | 605 | 613 | PF00400 | 0.521 |
LIG_EVH1_2 | 516 | 520 | PF00568 | 0.521 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.543 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.526 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.509 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.305 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.497 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.503 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.432 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.537 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.422 |
LIG_FHA_1 | 766 | 772 | PF00498 | 0.451 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.677 |
LIG_FHA_1 | 894 | 900 | PF00498 | 0.379 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.573 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.624 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.455 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.432 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.521 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.521 |
LIG_FHA_2 | 625 | 631 | PF00498 | 0.539 |
LIG_FHA_2 | 819 | 825 | PF00498 | 0.737 |
LIG_FHA_2 | 882 | 888 | PF00498 | 0.498 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.682 |
LIG_GBD_Chelix_1 | 663 | 671 | PF00786 | 0.370 |
LIG_Integrin_RGD_1 | 602 | 604 | PF01839 | 0.214 |
LIG_LIR_Apic_2 | 148 | 153 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 292 | 296 | PF02991 | 0.387 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 643 | 648 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 385 | 393 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 604 | 612 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 889 | 900 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 604 | 608 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 776 | 782 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 889 | 895 | PF02991 | 0.483 |
LIG_LYPXL_S_1 | 203 | 207 | PF13949 | 0.447 |
LIG_LYPXL_SIV_4 | 437 | 445 | PF13949 | 0.487 |
LIG_LYPXL_yS_3 | 204 | 207 | PF13949 | 0.440 |
LIG_NRBOX | 897 | 903 | PF00104 | 0.206 |
LIG_PCNA_yPIPBox_3 | 529 | 542 | PF02747 | 0.462 |
LIG_Pex14_1 | 641 | 645 | PF04695 | 0.446 |
LIG_Pex14_2 | 400 | 404 | PF04695 | 0.432 |
LIG_Pex14_3 | 531 | 536 | PF04695 | 0.446 |
LIG_PTB_Apo_2 | 275 | 282 | PF02174 | 0.485 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.454 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.470 |
LIG_SH2_CRK | 766 | 770 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 438 | 442 | PF00017 | 0.432 |
LIG_SH2_NCK_1 | 766 | 770 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 614 | 618 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 742 | 746 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 782 | 786 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.471 |
LIG_SH3_1 | 375 | 381 | PF00018 | 0.476 |
LIG_SH3_1 | 559 | 565 | PF00018 | 0.521 |
LIG_SH3_1 | 756 | 762 | PF00018 | 0.508 |
LIG_SH3_1 | 928 | 934 | PF00018 | 0.476 |
LIG_SH3_2 | 378 | 383 | PF14604 | 0.459 |
LIG_SH3_2 | 562 | 567 | PF14604 | 0.521 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.544 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.459 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.499 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.500 |
LIG_SH3_3 | 634 | 640 | PF00018 | 0.529 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.587 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.483 |
LIG_SH3_3 | 928 | 934 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 767 | 773 | PF11976 | 0.443 |
LIG_SUMO_SIM_anti_2 | 896 | 903 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 311 | 319 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 896 | 903 | PF11976 | 0.370 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.556 |
LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.492 |
LIG_TRAF2_1 | 884 | 887 | PF00917 | 0.530 |
LIG_TYR_ITIM | 551 | 556 | PF00017 | 0.329 |
LIG_UBA3_1 | 480 | 486 | PF00899 | 0.277 |
LIG_UBA3_1 | 593 | 599 | PF00899 | 0.379 |
LIG_UBA3_1 | 748 | 756 | PF00899 | 0.479 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.483 |
LIG_WRPW_2 | 197 | 200 | PF00400 | 0.452 |
MOD_CDC14_SPxK_1 | 647 | 650 | PF00782 | 0.275 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.471 |
MOD_CDK_SPxK_1 | 644 | 650 | PF00069 | 0.275 |
MOD_CDK_SPxxK_3 | 644 | 651 | PF00069 | 0.275 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.501 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.432 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.299 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.359 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.712 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.576 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.577 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.497 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.360 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.380 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.350 |
MOD_CK2_1 | 785 | 791 | PF00069 | 0.474 |
MOD_CK2_1 | 881 | 887 | PF00069 | 0.452 |
MOD_CK2_1 | 933 | 939 | PF00069 | 0.550 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.726 |
MOD_Cter_Amidation | 304 | 307 | PF01082 | 0.389 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.515 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.393 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.332 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.510 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.401 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.496 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.478 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.487 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.721 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.688 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.590 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.498 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.515 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.401 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.419 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.465 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.326 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.285 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.497 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.736 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.692 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.564 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.435 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.432 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.401 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.468 |
MOD_N-GLC_1 | 794 | 799 | PF02516 | 0.564 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.678 |
MOD_N-GLC_2 | 726 | 728 | PF02516 | 0.504 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.275 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.463 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.275 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.336 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.464 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.520 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.490 |
MOD_NEK2_1 | 902 | 907 | PF00069 | 0.511 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.328 |
MOD_PIKK_1 | 822 | 828 | PF00454 | 0.541 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.393 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.299 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.260 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.481 |
MOD_PKA_2 | 909 | 915 | PF00069 | 0.531 |
MOD_PKB_1 | 19 | 27 | PF00069 | 0.381 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.482 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.287 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.530 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.558 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.275 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.123 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.489 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.271 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.349 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.468 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.393 |
MOD_Plk_2-3 | 785 | 791 | PF00069 | 0.462 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.351 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.480 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.401 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.533 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.390 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.496 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.275 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.301 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.329 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.410 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.410 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.452 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.508 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.520 |
MOD_Plk_4 | 933 | 939 | PF00069 | 0.547 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.508 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.466 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.455 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.308 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.438 |
MOD_SUMO_rev_2 | 390 | 399 | PF00179 | 0.353 |
TRG_AP2beta_CARGO_1 | 533 | 542 | PF09066 | 0.275 |
TRG_DiLeu_BaEn_1 | 533 | 538 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_1 | 776 | 781 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 897 | 902 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_4 | 386 | 392 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_4 | 533 | 539 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 649 | 651 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 851 | 853 | PF00400 | 0.759 |
TRG_ER_diArg_1 | 927 | 929 | PF00400 | 0.493 |
TRG_NES_CRM1_1 | 763 | 776 | PF08389 | 0.408 |
TRG_NES_CRM1_1 | 893 | 908 | PF08389 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.275 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.275 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ70 | Leptomonas seymouri | 60% | 99% |
A0A0S4KIX9 | Bodo saltans | 36% | 100% |
A0A1X0NYL5 | Trypanosomatidae | 41% | 97% |
A0A3Q8IHX8 | Leishmania donovani | 93% | 100% |
A0A422P1Q3 | Trypanosoma rangeli | 40% | 100% |
A0JN80 | Bos taurus | 27% | 89% |
A2RV18 | Danio rerio | 28% | 89% |
A4HG84 | Leishmania braziliensis | 81% | 99% |
A4I3A3 | Leishmania infantum | 93% | 100% |
D0A826 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
O14040 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P0DM58 | Arabidopsis thaliana | 30% | 89% |
Q08162 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 94% |
Q0P4R5 | Xenopus tropicalis | 27% | 91% |
Q0V9R3 | Xenopus tropicalis | 30% | 100% |
Q0WPN0 | Arabidopsis thaliana | 30% | 89% |
Q4Q8M6 | Leishmania major | 92% | 100% |
Q5R5N8 | Pongo abelii | 27% | 89% |
Q5U2P0 | Rattus norvegicus | 27% | 89% |
Q6GN11 | Xenopus laevis | 27% | 90% |
Q8C0S1 | Mus musculus | 27% | 89% |
Q8TF46 | Homo sapiens | 28% | 89% |