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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HJQ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000459 | exonucleolytic trimming involved in rRNA processing | 8 | 6 |
GO:0000467 | exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 6 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 6 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006364 | rRNA processing | 8 | 6 |
GO:0006396 | RNA processing | 6 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016072 | rRNA metabolic process | 7 | 6 |
GO:0031123 | RNA 3'-end processing | 7 | 6 |
GO:0031125 | rRNA 3'-end processing | 9 | 6 |
GO:0034470 | ncRNA processing | 7 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034660 | ncRNA metabolic process | 6 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 6 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 6 |
GO:0090503 | RNA phosphodiester bond hydrolysis, exonucleolytic | 7 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 6 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004518 | nuclease activity | 4 | 8 |
GO:0004527 | exonuclease activity | 5 | 8 |
GO:0004532 | RNA exonuclease activity | 5 | 6 |
GO:0004540 | RNA nuclease activity | 4 | 6 |
GO:0005488 | binding | 1 | 10 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 7 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 6 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.417 |
CLV_C14_Caspase3-7 | 730 | 734 | PF00656 | 0.357 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.556 |
CLV_PCSK_FUR_1 | 677 | 681 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 756 | 760 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 861 | 865 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.527 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.452 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.435 |
DEG_APCC_DBOX_1 | 621 | 629 | PF00400 | 0.267 |
DEG_APCC_DBOX_1 | 755 | 763 | PF00400 | 0.446 |
DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.497 |
DEG_MDM2_SWIB_1 | 57 | 65 | PF02201 | 0.438 |
DEG_SPOP_SBC_1 | 575 | 579 | PF00917 | 0.312 |
DOC_CDC14_PxL_1 | 457 | 465 | PF14671 | 0.317 |
DOC_CDC14_PxL_1 | 801 | 809 | PF14671 | 0.517 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.470 |
DOC_CKS1_1 | 588 | 593 | PF01111 | 0.575 |
DOC_CYCLIN_RxL_1 | 627 | 641 | PF00134 | 0.373 |
DOC_CYCLIN_RxL_1 | 855 | 868 | PF00134 | 0.402 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 168 | 176 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 182 | 192 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 479 | 487 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 185 | 192 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 451 | 459 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 422 | 429 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.267 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.578 |
DOC_PP4_FxxP_1 | 547 | 550 | PF00568 | 0.409 |
DOC_SPAK_OSR1_1 | 497 | 501 | PF12202 | 0.337 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 832 | 837 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 903 | 908 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 142 | 152 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 511 | 521 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 576 | 581 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 585 | 591 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 704 | 708 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 713 | 719 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 887 | 893 | PF00244 | 0.331 |
LIG_AP2alpha_2 | 129 | 131 | PF02296 | 0.489 |
LIG_APCC_ABBA_1 | 174 | 179 | PF00400 | 0.431 |
LIG_APCC_ABBA_1 | 181 | 186 | PF00400 | 0.452 |
LIG_APCC_ABBA_1 | 635 | 640 | PF00400 | 0.309 |
LIG_BRCT_BRCA1_1 | 853 | 857 | PF00533 | 0.357 |
LIG_DLG_GKlike_1 | 226 | 233 | PF00625 | 0.438 |
LIG_EH1_1 | 856 | 864 | PF00400 | 0.431 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.330 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.478 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.520 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.428 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.467 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.378 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.463 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.578 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.667 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.467 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.313 |
LIG_FHA_2 | 794 | 800 | PF00498 | 0.521 |
LIG_FHA_2 | 806 | 812 | PF00498 | 0.602 |
LIG_FHA_2 | 904 | 910 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 545 | 550 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 844 | 850 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 518 | 527 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 560 | 570 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 614 | 619 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 854 | 864 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 518 | 522 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 560 | 565 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 614 | 618 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 717 | 722 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 854 | 860 | PF02991 | 0.347 |
LIG_LYPXL_S_1 | 718 | 722 | PF13949 | 0.394 |
LIG_LYPXL_yS_3 | 187 | 190 | PF13949 | 0.459 |
LIG_Pex14_1 | 847 | 851 | PF04695 | 0.366 |
LIG_Pex14_1 | 888 | 892 | PF04695 | 0.326 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.376 |
LIG_Pex14_2 | 884 | 888 | PF04695 | 0.332 |
LIG_Rb_LxCxE_1 | 312 | 333 | PF01857 | 0.542 |
LIG_REV1ctd_RIR_1 | 719 | 730 | PF16727 | 0.501 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.354 |
LIG_SH2_CRK | 519 | 523 | PF00017 | 0.325 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 157 | 160 | PF00017 | 0.248 |
LIG_SH2_GRB2like | 392 | 395 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 392 | 396 | PF00017 | 0.378 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.382 |
LIG_SH2_SRC | 562 | 565 | PF00017 | 0.444 |
LIG_SH2_SRC | 580 | 583 | PF00017 | 0.291 |
LIG_SH2_SRC | 851 | 854 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 477 | 480 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.475 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.495 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.414 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.454 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.452 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.693 |
LIG_SH3_3 | 811 | 817 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 149 | 155 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 194 | 200 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 520 | 525 | PF11976 | 0.323 |
LIG_SUMO_SIM_anti_2 | 614 | 620 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 197 | 203 | PF11976 | 0.435 |
LIG_TRAF2_1 | 437 | 440 | PF00917 | 0.429 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.481 |
LIG_TRAF2_2 | 814 | 819 | PF00917 | 0.479 |
LIG_TYR_ITIM | 534 | 539 | PF00017 | 0.307 |
LIG_TYR_ITIM | 637 | 642 | PF00017 | 0.306 |
LIG_WRC_WIRS_1 | 331 | 336 | PF05994 | 0.444 |
LIG_WRC_WIRS_1 | 628 | 633 | PF05994 | 0.428 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.305 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.471 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.543 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.693 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.409 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.395 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.450 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.721 |
MOD_CK1_1 | 868 | 874 | PF00069 | 0.514 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.348 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.395 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.406 |
MOD_CK2_1 | 793 | 799 | PF00069 | 0.519 |
MOD_CK2_1 | 805 | 811 | PF00069 | 0.597 |
MOD_CK2_1 | 888 | 894 | PF00069 | 0.472 |
MOD_Cter_Amidation | 241 | 244 | PF01082 | 0.293 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.609 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.466 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.606 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.657 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.523 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.457 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.473 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.665 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.565 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.695 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.571 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.707 |
MOD_GlcNHglycan | 836 | 839 | PF01048 | 0.553 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.650 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.489 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.564 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.381 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.418 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.723 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.449 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.735 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.314 |
MOD_LATS_1 | 213 | 219 | PF00433 | 0.500 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.507 |
MOD_N-GLC_1 | 782 | 787 | PF02516 | 0.508 |
MOD_N-GLC_2 | 235 | 237 | PF02516 | 0.414 |
MOD_N-GLC_2 | 484 | 486 | PF02516 | 0.335 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.594 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.526 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.430 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.370 |
MOD_NEK2_1 | 757 | 762 | PF00069 | 0.491 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.446 |
MOD_NEK2_2 | 638 | 643 | PF00069 | 0.311 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.301 |
MOD_PIKK_1 | 683 | 689 | PF00454 | 0.495 |
MOD_PIKK_1 | 828 | 834 | PF00454 | 0.667 |
MOD_PK_1 | 714 | 720 | PF00069 | 0.273 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.533 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.440 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.355 |
MOD_PKA_2 | 669 | 675 | PF00069 | 0.573 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.480 |
MOD_PKA_2 | 773 | 779 | PF00069 | 0.663 |
MOD_PKA_2 | 888 | 894 | PF00069 | 0.398 |
MOD_PKB_1 | 681 | 689 | PF00069 | 0.599 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.323 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.664 |
MOD_Plk_1 | 868 | 874 | PF00069 | 0.381 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.314 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.338 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.643 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.426 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.393 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.398 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.381 |
MOD_Plk_4 | 888 | 894 | PF00069 | 0.396 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.425 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.494 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.694 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.689 |
MOD_ProDKin_1 | 832 | 838 | PF00069 | 0.675 |
MOD_ProDKin_1 | 903 | 909 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 179 | 183 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 214 | 223 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 438 | 443 | PF00179 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 530 | 535 | PF01217 | 0.313 |
TRG_DiLeu_BaLyEn_6 | 858 | 863 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 719 | 722 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 605 | 608 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 642 | 644 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 677 | 680 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 724 | 726 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 191 | 203 | PF08389 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 22 | 27 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 243 | 248 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 735 | 739 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 861 | 865 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJE4 | Leptomonas seymouri | 52% | 99% |
A0A1X0NK05 | Trypanosomatidae | 34% | 100% |
A0A3Q8ISV5 | Leishmania donovani | 78% | 100% |
A0A422NPF9 | Trypanosoma rangeli | 35% | 100% |
A4I774 | Leishmania infantum | 78% | 100% |
E9B268 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q5Z1 | Leishmania major | 76% | 100% |
V5D1X6 | Trypanosoma cruzi | 36% | 100% |