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:0005730 | nucleolus | 5 | 2 |
GO:0030684 | preribosome | 3 | 2 |
GO:0030686 | 90S preribosome | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 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:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: E9AET3
Term | Name | Level | Count |
---|---|---|---|
GO:0000447 | endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 2 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 2 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 2 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.701 |
CLV_C14_Caspase3-7 | 1007 | 1011 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.787 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 832 | 836 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 863 | 867 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 981 | 985 | PF00656 | 0.627 |
CLV_MEL_PAP_1 | 275 | 281 | PF00089 | 0.688 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 929 | 931 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 944 | 946 | PF00675 | 0.542 |
CLV_PCSK_FUR_1 | 50 | 54 | PF00082 | 0.621 |
CLV_PCSK_FUR_1 | 620 | 624 | PF00082 | 0.563 |
CLV_PCSK_FUR_1 | 921 | 925 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 923 | 925 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 928 | 930 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 974 | 976 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 645 | 647 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 974 | 976 | PF00082 | 0.638 |
CLV_PCSK_PC7_1 | 343 | 349 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 924 | 930 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.432 |
CLV_Separin_Metazoa | 419 | 423 | PF03568 | 0.760 |
DEG_APCC_DBOX_1 | 386 | 394 | PF00400 | 0.671 |
DEG_APCC_DBOX_1 | 817 | 825 | PF00400 | 0.622 |
DEG_Kelch_Keap1_1 | 520 | 525 | PF01344 | 0.737 |
DEG_Kelch_Keap1_1 | 732 | 737 | PF01344 | 0.408 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.793 |
DEG_SPOP_SBC_1 | 949 | 953 | PF00917 | 0.549 |
DOC_ANK_TNKS_1 | 136 | 143 | PF00023 | 0.718 |
DOC_CYCLIN_yCln2_LP_2 | 692 | 698 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 766 | 772 | PF00134 | 0.517 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.739 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 271 | 279 | PF00069 | 0.663 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.748 |
DOC_PP2B_LxvP_1 | 692 | 695 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 987 | 990 | PF13499 | 0.707 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.484 |
DOC_PP4_FxxP_1 | 597 | 600 | PF00568 | 0.631 |
DOC_USP7_MATH_1 | 1004 | 1008 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 1011 | 1015 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 756 | 760 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 862 | 866 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.650 |
DOC_USP7_UBL2_3 | 350 | 354 | PF12436 | 0.683 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.735 |
DOC_USP7_UBL2_3 | 774 | 778 | PF12436 | 0.740 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.810 |
LIG_14-3-3_CanoR_1 | 123 | 133 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 449 | 458 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 841 | 847 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 263 | 280 | PF00022 | 0.632 |
LIG_AP2alpha_1 | 786 | 790 | PF02296 | 0.781 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.688 |
LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.680 |
LIG_BRCT_BRCA1_1 | 872 | 876 | PF00533 | 0.408 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.784 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.618 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.688 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.664 |
LIG_FHA_1 | 740 | 746 | PF00498 | 0.690 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.608 |
LIG_FHA_1 | 885 | 891 | PF00498 | 0.344 |
LIG_FHA_1 | 950 | 956 | PF00498 | 0.549 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.711 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.665 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.540 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.691 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.691 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.598 |
LIG_FHA_2 | 832 | 838 | PF00498 | 0.646 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.330 |
LIG_GBD_Chelix_1 | 968 | 976 | PF00786 | 0.634 |
LIG_LIR_Apic_2 | 596 | 600 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 415 | 426 | PF02991 | 0.743 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.742 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.729 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 800 | 806 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 850 | 856 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 943 | 949 | PF02991 | 0.514 |
LIG_LYPXL_L_2 | 805 | 814 | PF13949 | 0.629 |
LIG_Pex14_1 | 566 | 570 | PF04695 | 0.504 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.515 |
LIG_Pex14_2 | 786 | 790 | PF04695 | 0.781 |
LIG_Rb_pABgroove_1 | 703 | 711 | PF01858 | 0.485 |
LIG_RPA_C_Fungi | 397 | 409 | PF08784 | 0.416 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.544 |
LIG_SH2_CRK | 946 | 950 | PF00017 | 0.617 |
LIG_SH2_GRB2like | 543 | 546 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 910 | 914 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.611 |
LIG_SH2_STAT3 | 575 | 578 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 913 | 916 | PF00017 | 0.344 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.768 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.782 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.768 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.444 |
LIG_SH3_3 | 980 | 986 | PF00018 | 0.686 |
LIG_SUMO_SIM_par_1 | 884 | 892 | PF11976 | 0.347 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.728 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.591 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.436 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.612 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.751 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.604 |
LIG_TRAF2_1 | 759 | 762 | PF00917 | 0.572 |
LIG_TRAF2_1 | 889 | 892 | PF00917 | 0.344 |
LIG_TRAF2_2 | 957 | 962 | PF00917 | 0.712 |
LIG_TRFH_1 | 803 | 807 | PF08558 | 0.448 |
LIG_UBA3_1 | 838 | 847 | PF00899 | 0.575 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.612 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.778 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.745 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.595 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.623 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.766 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.691 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.789 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.608 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.716 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.796 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.663 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.721 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.761 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.693 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.520 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.652 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.704 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.567 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.644 |
MOD_CK2_1 | 886 | 892 | PF00069 | 0.344 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.764 |
MOD_Cter_Amidation | 164 | 167 | PF01082 | 0.745 |
MOD_Cter_Amidation | 475 | 478 | PF01082 | 0.754 |
MOD_GlcNHglycan | 1027 | 1030 | PF01048 | 0.749 |
MOD_GlcNHglycan | 1035 | 1038 | PF01048 | 0.727 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.707 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.778 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.770 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.635 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.717 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.744 |
MOD_GlcNHglycan | 537 | 541 | PF01048 | 0.743 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.715 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.713 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.666 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.408 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.658 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.768 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.800 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.415 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.795 |
MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.775 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.811 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.734 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.567 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.798 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.698 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.709 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.676 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.605 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.707 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.637 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.583 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.660 |
MOD_N-GLC_1 | 739 | 744 | PF02516 | 0.603 |
MOD_N-GLC_1 | 970 | 975 | PF02516 | 0.607 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.698 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.616 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.604 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.333 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.672 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.519 |
MOD_PKA_1 | 271 | 277 | PF00069 | 0.526 |
MOD_PKA_1 | 511 | 517 | PF00069 | 0.677 |
MOD_PKA_2 | 1025 | 1031 | PF00069 | 0.755 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.701 |
MOD_PKA_2 | 940 | 946 | PF00069 | 0.546 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.587 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.344 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.587 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.627 |
MOD_Plk_2-3 | 238 | 244 | PF00069 | 0.689 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.726 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.686 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.642 |
MOD_Plk_4 | 950 | 956 | PF00069 | 0.623 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.823 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.811 |
MOD_SUMO_for_1 | 316 | 319 | PF00179 | 0.641 |
MOD_SUMO_rev_2 | 103 | 113 | PF00179 | 0.799 |
MOD_SUMO_rev_2 | 361 | 366 | PF00179 | 0.644 |
MOD_SUMO_rev_2 | 452 | 458 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 636 | 641 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 697 | 706 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 958 | 968 | PF00179 | 0.574 |
TRG_DiLeu_BaEn_1 | 454 | 459 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_1 | 762 | 767 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_4 | 636 | 642 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_4 | 851 | 857 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_4 | 891 | 897 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.553 |
TRG_DiLeu_LyEn_5 | 454 | 459 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 853 | 856 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 878 | 881 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 928 | 930 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 944 | 946 | PF00400 | 0.546 |
TRG_NLS_Bipartite_1 | 156 | 170 | PF00514 | 0.596 |
TRG_NLS_Bipartite_1 | 271 | 288 | PF00514 | 0.642 |
TRG_NLS_Bipartite_1 | 622 | 643 | PF00514 | 0.444 |
TRG_NLS_MonoExtC_3 | 390 | 395 | PF00514 | 0.663 |
TRG_NLS_MonoExtC_3 | 510 | 515 | PF00514 | 0.743 |
TRG_NLS_MonoExtC_3 | 775 | 780 | PF00514 | 0.771 |
TRG_NLS_MonoExtN_4 | 511 | 516 | PF00514 | 0.679 |
TRG_NLS_MonoExtN_4 | 774 | 781 | PF00514 | 0.772 |
TRG_Pf-PMV_PEXEL_1 | 391 | 396 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 974 | 978 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY8 | Leptomonas seymouri | 61% | 100% |
A0A3R7NCJ6 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X904 | Leishmania donovani | 92% | 100% |
A4HFF6 | Leishmania braziliensis | 80% | 99% |
A4IB05 | Leishmania infantum | 93% | 100% |
C9ZNK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B5Y8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5ATL2 | Trypanosoma cruzi | 37% | 100% |