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:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030686 | 90S preribosome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9B5Y8
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 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1006 | 1010 | PF00656 | 0.745 |
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.445 |
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.816 |
CLV_C14_Caspase3-7 | 614 | 618 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 831 | 835 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 980 | 984 | PF00656 | 0.665 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 701 | 703 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 928 | 930 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 943 | 945 | PF00675 | 0.541 |
CLV_PCSK_FUR_1 | 619 | 623 | PF00082 | 0.551 |
CLV_PCSK_FUR_1 | 920 | 924 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 927 | 929 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 973 | 975 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 638 | 640 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 644 | 646 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 973 | 975 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 344 | 350 | PF00082 | 0.660 |
CLV_PCSK_PC7_1 | 923 | 929 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.475 |
CLV_Separin_Metazoa | 420 | 424 | PF03568 | 0.730 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.701 |
DEG_APCC_DBOX_1 | 816 | 824 | PF00400 | 0.629 |
DEG_Kelch_Keap1_1 | 521 | 526 | PF01344 | 0.735 |
DEG_Kelch_Keap1_1 | 731 | 736 | PF01344 | 0.398 |
DEG_SCF_FBW7_1 | 2 | 9 | PF00400 | 0.481 |
DEG_SCF_TRCP1_1 | 523 | 528 | PF00400 | 0.518 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.651 |
DOC_ANK_TNKS_1 | 137 | 144 | PF00023 | 0.704 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.482 |
DOC_CYCLIN_yCln2_LP_2 | 691 | 697 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 220 | 229 | PF00069 | 0.740 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 775 | 785 | PF00069 | 0.693 |
DOC_MAPK_MEF2A_6 | 272 | 280 | PF00069 | 0.648 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.751 |
DOC_PP2B_LxvP_1 | 691 | 694 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 986 | 989 | PF13499 | 0.687 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 596 | 599 | PF00568 | 0.597 |
DOC_USP7_MATH_1 | 1003 | 1007 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 755 | 759 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 861 | 865 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 869 | 873 | PF00917 | 0.343 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.620 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.683 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.721 |
DOC_USP7_UBL2_3 | 773 | 777 | PF12436 | 0.717 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.798 |
LIG_14-3-3_CanoR_1 | 1023 | 1033 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 423 | 433 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 450 | 459 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 840 | 846 | PF00244 | 0.573 |
LIG_Actin_WH2_2 | 264 | 281 | PF00022 | 0.621 |
LIG_AP2alpha_1 | 785 | 789 | PF02296 | 0.749 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 871 | 875 | PF00533 | 0.398 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.774 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.618 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.702 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.712 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.540 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.603 |
LIG_FHA_1 | 884 | 890 | PF00498 | 0.344 |
LIG_FHA_1 | 949 | 955 | PF00498 | 0.537 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.743 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.732 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.659 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.525 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.617 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.588 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.644 |
LIG_GBD_Chelix_1 | 967 | 975 | PF00786 | 0.595 |
LIG_GSK3_LRP6_1 | 2 | 8 | PF00069 | 0.477 |
LIG_IRF3_LxIS_1 | 276 | 281 | PF10401 | 0.411 |
LIG_LIR_Apic_2 | 595 | 599 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 416 | 425 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 541 | 550 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 849 | 855 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 942 | 948 | PF02991 | 0.487 |
LIG_LYPXL_L_2 | 804 | 813 | PF13949 | 0.613 |
LIG_NRP_CendR_1 | 1047 | 1048 | PF00754 | 0.752 |
LIG_Pex14_1 | 565 | 569 | PF04695 | 0.491 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.493 |
LIG_Pex14_2 | 785 | 789 | PF04695 | 0.749 |
LIG_Rb_pABgroove_1 | 702 | 710 | PF01858 | 0.475 |
LIG_SH2_CRK | 543 | 547 | PF00017 | 0.550 |
LIG_SH2_CRK | 945 | 949 | PF00017 | 0.606 |
LIG_SH2_GRB2like | 542 | 545 | PF00017 | 0.632 |
LIG_SH2_NCK_1 | 429 | 433 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 909 | 913 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 574 | 577 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 725 | 728 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 912 | 915 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 991 | 994 | PF00017 | 0.496 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.762 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.770 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.742 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.449 |
LIG_SH3_3 | 979 | 985 | PF00018 | 0.685 |
LIG_SUMO_SIM_anti_2 | 798 | 805 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 883 | 891 | PF11976 | 0.346 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.762 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.619 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.583 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.444 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.567 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.680 |
LIG_TRAF2_1 | 758 | 761 | PF00917 | 0.572 |
LIG_TRAF2_1 | 888 | 891 | PF00917 | 0.344 |
LIG_TRAF2_2 | 956 | 961 | PF00917 | 0.688 |
LIG_UBA3_1 | 837 | 846 | PF00899 | 0.581 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.711 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.604 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.769 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.576 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.592 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.515 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.738 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.729 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.622 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.712 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.750 |
MOD_CK1_1 | 938 | 944 | PF00069 | 0.591 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.693 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.752 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.685 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.760 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.640 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.746 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.764 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.518 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.739 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.551 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.699 |
MOD_CK2_1 | 755 | 761 | PF00069 | 0.588 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.652 |
MOD_CK2_1 | 885 | 891 | PF00069 | 0.344 |
MOD_Cter_Amidation | 1045 | 1048 | PF01082 | 0.623 |
MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.771 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.522 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.709 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.780 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.777 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.784 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.596 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.739 |
MOD_GlcNHglycan | 535 | 540 | PF01048 | 0.766 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.721 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.673 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.398 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.717 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.789 |
MOD_GlcNHglycan | 871 | 874 | PF01048 | 0.405 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.780 |
MOD_GSK3_1 | 1004 | 1011 | PF00069 | 0.764 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.472 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.736 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.701 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.551 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.752 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.754 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.757 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.559 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.710 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.682 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.697 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.650 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.672 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.562 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.726 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.640 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.574 |
MOD_N-GLC_1 | 969 | 974 | PF02516 | 0.603 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.754 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.698 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.607 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.625 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.344 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.671 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.533 |
MOD_NEK2_2 | 1024 | 1029 | PF00069 | 0.484 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.621 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.538 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.681 |
MOD_PKA_2 | 1024 | 1030 | PF00069 | 0.735 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.702 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.516 |
MOD_Plk_1 | 1008 | 1014 | PF00069 | 0.492 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.546 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.578 |
MOD_Plk_1 | 883 | 889 | PF00069 | 0.344 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.738 |
MOD_Plk_2-3 | 182 | 188 | PF00069 | 0.722 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.629 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.686 |
MOD_Plk_2-3 | 488 | 494 | PF00069 | 0.609 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.681 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.603 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.645 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.818 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.477 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.797 |
MOD_SUMO_for_1 | 317 | 320 | PF00179 | 0.636 |
MOD_SUMO_rev_2 | 104 | 114 | PF00179 | 0.783 |
MOD_SUMO_rev_2 | 362 | 367 | PF00179 | 0.638 |
MOD_SUMO_rev_2 | 400 | 404 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 453 | 459 | PF00179 | 0.542 |
MOD_SUMO_rev_2 | 635 | 640 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 696 | 705 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 709 | 718 | PF00179 | 0.335 |
TRG_DiLeu_BaEn_3 | 760 | 766 | PF01217 | 0.573 |
TRG_DiLeu_BaEn_3 | 962 | 968 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_4 | 461 | 467 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_4 | 635 | 641 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_4 | 850 | 856 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_4 | 890 | 896 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 455 | 460 | PF01217 | 0.397 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 852 | 855 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 877 | 880 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 945 | 948 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 619 | 622 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 817 | 820 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 922 | 924 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 927 | 929 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 943 | 945 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 992 | 995 | PF00400 | 0.616 |
TRG_NLS_Bipartite_1 | 157 | 171 | PF00514 | 0.599 |
TRG_NLS_Bipartite_1 | 272 | 289 | PF00514 | 0.626 |
TRG_NLS_Bipartite_1 | 457 | 478 | PF00514 | 0.493 |
TRG_NLS_Bipartite_1 | 621 | 642 | PF00514 | 0.415 |
TRG_NLS_MonoExtC_3 | 391 | 396 | PF00514 | 0.654 |
TRG_NLS_MonoExtC_3 | 473 | 478 | PF00514 | 0.454 |
TRG_NLS_MonoExtC_3 | 511 | 516 | PF00514 | 0.752 |
TRG_NLS_MonoExtC_3 | 774 | 779 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 282 | 289 | PF00514 | 0.609 |
TRG_NLS_MonoExtN_4 | 474 | 481 | PF00514 | 0.592 |
TRG_NLS_MonoExtN_4 | 512 | 517 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 773 | 780 | PF00514 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 598 | 602 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 973 | 977 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY8 | Leptomonas seymouri | 61% | 99% |
A0A0S4JTV9 | Bodo saltans | 34% | 100% |
A0A1X0NGP0 | Trypanosomatidae | 39% | 100% |
A0A3R7NCJ6 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X904 | Leishmania donovani | 90% | 100% |
A4HFF6 | Leishmania braziliensis | 78% | 100% |
A4IB05 | Leishmania infantum | 90% | 100% |
C9ZNK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AET3 | Leishmania major | 91% | 100% |
V5ATL2 | Trypanosoma cruzi | 36% | 100% |