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:0000176 | nuclear exosome (RNase complex) | 3 | 1 |
GO:0000177 | cytoplasmic exosome (RNase complex) | 5 | 1 |
GO:0000178 | exosome (RNase complex) | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905354 | exoribonuclease complex | 3 | 1 |
GO:0005634 | nucleus | 5 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HG74
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006401 | RNA catabolic process | 5 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0016075 | rRNA catabolic process | 7 | 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:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0034661 | ncRNA catabolic process | 6 | 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: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 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 12 |
GO:0004540 | RNA nuclease activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 1 |
GO:0004519 | endonuclease activity | 5 | 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 | 631 | 635 | PF00656 | 0.558 |
CLV_MEL_PAP_1 | 258 | 264 | PF00089 | 0.301 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.253 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 713 | 715 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 831 | 833 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 905 | 907 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 831 | 833 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 905 | 907 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 840 | 844 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 905 | 909 | PF00082 | 0.486 |
CLV_Separin_Metazoa | 542 | 546 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 810 | 818 | PF00400 | 0.543 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.485 |
DEG_SCF_FBW7_1 | 164 | 170 | PF00400 | 0.335 |
DOC_ANK_TNKS_1 | 905 | 912 | PF00023 | 0.700 |
DOC_CDC14_PxL_1 | 467 | 475 | PF14671 | 0.453 |
DOC_CDC14_PxL_1 | 814 | 822 | PF14671 | 0.422 |
DOC_CKS1_1 | 164 | 169 | PF01111 | 0.426 |
DOC_MAPK_DCC_7 | 306 | 315 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 292 | 301 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 326 | 332 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 455 | 462 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 554 | 562 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 713 | 720 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 823 | 830 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 130 | 137 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 162 | 171 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 295 | 303 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 823 | 830 | PF00069 | 0.390 |
DOC_MAPK_NFAT4_5 | 130 | 138 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 838 | 844 | PF00149 | 0.519 |
DOC_PP2B_LxvP_1 | 700 | 703 | PF13499 | 0.453 |
DOC_PP2B_PxIxI_1 | 310 | 316 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 708 | 711 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 731 | 735 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 892 | 896 | PF00917 | 0.584 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 327 | 331 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 456 | 461 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 672 | 679 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 790 | 798 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 664 | 682 | PF00022 | 0.453 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.453 |
LIG_CaM_IQ_9 | 19 | 34 | PF13499 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 333 | 341 | PF00928 | 0.446 |
LIG_eIF4E_1 | 30 | 36 | PF01652 | 0.308 |
LIG_eIF4E_1 | 612 | 618 | PF01652 | 0.465 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.578 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.453 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.521 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.465 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.453 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.514 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.453 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.453 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.453 |
LIG_FHA_1 | 837 | 843 | PF00498 | 0.469 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.564 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.504 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.467 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.453 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.487 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.461 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.424 |
LIG_GBD_Chelix_1 | 536 | 544 | PF00786 | 0.265 |
LIG_GBD_Chelix_1 | 841 | 849 | PF00786 | 0.451 |
LIG_LIR_Apic_2 | 237 | 242 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 706 | 711 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 131 | 138 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 626 | 637 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 664 | 674 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 693 | 703 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 794 | 803 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 862 | 872 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 594 | 599 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 626 | 632 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 693 | 698 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 794 | 800 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 862 | 868 | PF02991 | 0.674 |
LIG_MLH1_MIPbox_1 | 193 | 197 | PF16413 | 0.539 |
LIG_NRBOX | 32 | 38 | PF00104 | 0.462 |
LIG_OCRL_FandH_1 | 636 | 648 | PF00620 | 0.378 |
LIG_PDZ_Class_1 | 915 | 920 | PF00595 | 0.743 |
LIG_Pex14_2 | 490 | 494 | PF04695 | 0.453 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 599 | 602 | PF00017 | 0.504 |
LIG_SH2_GRB2like | 666 | 669 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 599 | 603 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 865 | 869 | PF00017 | 0.706 |
LIG_SH2_PTP2 | 132 | 135 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 346 | 349 | PF00017 | 0.453 |
LIG_SH2_SRC | 346 | 349 | PF00017 | 0.453 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.514 |
LIG_SH2_SRC | 715 | 718 | PF00017 | 0.453 |
LIG_SH2_SRC | 865 | 868 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 599 | 603 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 715 | 719 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.373 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.494 |
LIG_SH3_3 | 795 | 801 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 361 | 366 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 95 | 103 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 11 | 17 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 357 | 366 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 404 | 409 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 95 | 103 | PF11976 | 0.544 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.597 |
LIG_TRAF2_1 | 563 | 566 | PF00917 | 0.465 |
LIG_TRAF2_1 | 782 | 785 | PF00917 | 0.506 |
LIG_TRFH_1 | 797 | 801 | PF08558 | 0.389 |
LIG_UBA3_1 | 543 | 551 | PF00899 | 0.322 |
LIG_WRC_WIRS_1 | 584 | 589 | PF05994 | 0.306 |
MOD_CDC14_SPxK_1 | 710 | 713 | PF00782 | 0.306 |
MOD_CDK_SPxK_1 | 707 | 713 | PF00069 | 0.306 |
MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.690 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.412 |
MOD_CDK_SPxxK_3 | 707 | 714 | PF00069 | 0.306 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.640 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.426 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.525 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.459 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.390 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.391 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.426 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.306 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.466 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.307 |
MOD_CK2_1 | 892 | 898 | PF00069 | 0.587 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.438 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.415 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.391 |
MOD_GlcNHglycan | 894 | 897 | PF01048 | 0.530 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.470 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.281 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.335 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.422 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.360 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.475 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.306 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.329 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.359 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.524 |
MOD_GSK3_1 | 911 | 918 | PF00069 | 0.739 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.519 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.639 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.306 |
MOD_N-GLC_2 | 477 | 479 | PF02516 | 0.306 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.374 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.271 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.564 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.524 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.426 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.306 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.306 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.306 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.571 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.306 |
MOD_PIKK_1 | 761 | 767 | PF00454 | 0.398 |
MOD_PK_1 | 326 | 332 | PF00069 | 0.322 |
MOD_PK_1 | 456 | 462 | PF00069 | 0.306 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.322 |
MOD_PKA_1 | 455 | 461 | PF00069 | 0.306 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.567 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.322 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.333 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.294 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.391 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.306 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.426 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.398 |
MOD_PKA_2 | 789 | 795 | PF00069 | 0.489 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.591 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.306 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.426 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.540 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.401 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.306 |
MOD_Plk_1 | 645 | 651 | PF00069 | 0.311 |
MOD_Plk_1 | 652 | 658 | PF00069 | 0.298 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.573 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.306 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.378 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.340 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.413 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.322 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.401 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.306 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.306 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.312 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.306 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.595 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.310 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.412 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.461 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.306 |
MOD_SUMO_for_1 | 691 | 694 | PF00179 | 0.426 |
MOD_SUMO_for_1 | 907 | 910 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 392 | 398 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 564 | 569 | PF00179 | 0.306 |
MOD_SUMO_rev_2 | 777 | 782 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 854 | 859 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_2 | 792 | 798 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 666 | 671 | PF01217 | 0.275 |
TRG_DiLeu_BaLyEn_6 | 841 | 846 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 865 | 868 | PF00928 | 0.701 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 512 | 515 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 712 | 714 | PF00400 | 0.306 |
TRG_NES_CRM1_1 | 399 | 409 | PF08389 | 0.306 |
TRG_NES_CRM1_1 | 630 | 646 | PF08389 | 0.391 |
TRG_NLS_MonoExtC_3 | 904 | 910 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 902 | 909 | PF00514 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 677 | 681 | PF00026 | 0.306 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Y7 | Leptomonas seymouri | 84% | 94% |
A0A0N1IJ70 | Leptomonas seymouri | 28% | 97% |
A0A0S4IQF4 | Bodo saltans | 61% | 92% |
A0A1X0NVC6 | Trypanosomatidae | 69% | 92% |
A0A3Q8IEN6 | Leishmania donovani | 90% | 100% |
A0A3R7NDR6 | Trypanosoma rangeli | 69% | 96% |
A0JN80 | Bos taurus | 34% | 87% |
A2RV18 | Danio rerio | 36% | 87% |
A4I3B7 | Leishmania infantum | 90% | 100% |
D0A7T6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 95% |
E9AZJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O14040 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 99% |
O74454 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 86% |
P24276 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 74% |
P37202 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 95% |
Q08162 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 92% |
Q09568 | Caenorhabditis elegans | 32% | 100% |
Q0P4R5 | Xenopus tropicalis | 34% | 89% |
Q17632 | Caenorhabditis elegans | 39% | 96% |
Q4Q8N7 | Leishmania major | 90% | 100% |
Q5R5N8 | Pongo abelii | 34% | 87% |
Q5U2P0 | Rattus norvegicus | 34% | 87% |
Q6GN11 | Xenopus laevis | 34% | 88% |
Q8C0S1 | Mus musculus | 34% | 87% |
Q8TF46 | Homo sapiens | 34% | 87% |
Q9CSH3 | Mus musculus | 40% | 96% |
Q9SHL7 | Arabidopsis thaliana | 40% | 99% |
Q9Y2L1 | Homo sapiens | 40% | 96% |
V5BIY4 | Trypanosoma cruzi | 70% | 95% |