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: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: A4IB05
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 | 101 | 105 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.826 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 832 | 836 | PF00656 | 0.663 |
CLV_C14_Caspase3-7 | 981 | 985 | PF00656 | 0.613 |
CLV_MEL_PAP_1 | 276 | 282 | PF00089 | 0.665 |
CLV_NRD_NRD_1 | 1000 | 1002 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 924 | 926 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 929 | 931 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 944 | 946 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 50 | 54 | PF00082 | 0.570 |
CLV_PCSK_FUR_1 | 620 | 624 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 921 | 925 | PF00082 | 0.447 |
CLV_PCSK_FUR_1 | 998 | 1002 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 1000 | 1002 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 923 | 925 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 928 | 930 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 974 | 976 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 993 | 995 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 645 | 647 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 974 | 976 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 993 | 995 | PF00082 | 0.738 |
CLV_PCSK_PC7_1 | 344 | 350 | PF00082 | 0.651 |
CLV_PCSK_PC7_1 | 924 | 930 | PF00082 | 0.381 |
CLV_PCSK_PC7_1 | 996 | 1002 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 420 | 424 | PF03568 | 0.725 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.708 |
DEG_Kelch_Keap1_1 | 520 | 525 | PF01344 | 0.723 |
DEG_Kelch_Keap1_1 | 732 | 737 | PF01344 | 0.402 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.789 |
DEG_SPOP_SBC_1 | 949 | 953 | PF00917 | 0.513 |
DOC_ANK_TNKS_1 | 137 | 144 | PF00023 | 0.707 |
DOC_CYCLIN_yCln2_LP_2 | 692 | 698 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 220 | 229 | PF00069 | 0.728 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 776 | 786 | PF00069 | 0.689 |
DOC_MAPK_gen_1 | 998 | 1007 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 272 | 280 | PF00069 | 0.640 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.750 |
DOC_PP2B_LxvP_1 | 692 | 695 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 987 | 990 | PF13499 | 0.696 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 597 | 600 | PF00568 | 0.595 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 756 | 760 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 862 | 866 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.348 |
DOC_USP7_UBL2_3 | 112 | 116 | PF12436 | 0.728 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.595 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.691 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 774 | 778 | PF12436 | 0.719 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 953 | 958 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 1009 | 1014 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 124 | 134 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 423 | 433 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 450 | 459 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 841 | 847 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 264 | 281 | PF00022 | 0.613 |
LIG_AP2alpha_1 | 786 | 790 | PF02296 | 0.767 |
LIG_APCC_ABBAyCdc20_2 | 53 | 59 | PF00400 | 0.537 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.668 |
LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.624 |
LIG_BRCT_BRCA1_1 | 872 | 876 | PF00533 | 0.402 |
LIG_CtBP_PxDLS_1 | 1004 | 1008 | PF00389 | 0.578 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.787 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.603 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.755 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.609 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.696 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.583 |
LIG_FHA_1 | 885 | 891 | PF00498 | 0.335 |
LIG_FHA_1 | 950 | 956 | PF00498 | 0.507 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.735 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.647 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.497 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.635 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.580 |
LIG_FHA_2 | 832 | 838 | PF00498 | 0.643 |
LIG_GBD_Chelix_1 | 968 | 976 | PF00786 | 0.616 |
LIG_IRF3_LxIS_1 | 464 | 469 | PF10401 | 0.378 |
LIG_LIR_Apic_2 | 596 | 600 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 416 | 425 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 850 | 856 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 943 | 949 | PF02991 | 0.506 |
LIG_LYPXL_L_2 | 805 | 814 | PF13949 | 0.609 |
LIG_PCNA_yPIPBox_3 | 816 | 825 | PF02747 | 0.451 |
LIG_Pex14_1 | 566 | 570 | PF04695 | 0.475 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.455 |
LIG_Pex14_2 | 786 | 790 | PF04695 | 0.767 |
LIG_Rb_pABgroove_1 | 703 | 711 | PF01858 | 0.480 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.502 |
LIG_SH2_CRK | 946 | 950 | PF00017 | 0.605 |
LIG_SH2_GRB2like | 543 | 546 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 429 | 433 | PF00017 | 0.701 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 910 | 914 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.594 |
LIG_SH2_STAT3 | 575 | 578 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 913 | 916 | PF00017 | 0.335 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.778 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.778 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.755 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.447 |
LIG_SH3_3 | 980 | 986 | PF00018 | 0.666 |
LIG_SUMO_SIM_anti_2 | 799 | 806 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 884 | 892 | PF11976 | 0.337 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.575 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.417 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.602 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.731 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.570 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.685 |
LIG_TRAF2_1 | 759 | 762 | PF00917 | 0.559 |
LIG_TRAF2_1 | 889 | 892 | PF00917 | 0.335 |
LIG_TRAF2_2 | 957 | 962 | PF00917 | 0.702 |
LIG_UBA3_1 | 838 | 847 | PF00899 | 0.578 |
LIG_WW_3 | 64 | 68 | PF00397 | 0.598 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.719 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.676 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.601 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.783 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.761 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.563 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.557 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.719 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.605 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.765 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.716 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.586 |
MOD_CK1_1 | 953 | 959 | PF00069 | 0.609 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.687 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.747 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.798 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.644 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.728 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.773 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.660 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.491 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.682 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.673 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.563 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.654 |
MOD_CK2_1 | 886 | 892 | PF00069 | 0.335 |
MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.756 |
MOD_Cter_Amidation | 476 | 479 | PF01082 | 0.726 |
MOD_Cter_Amidation | 998 | 1001 | PF01082 | 0.592 |
MOD_GlcNHglycan | 1029 | 1032 | PF01048 | 0.754 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.711 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.777 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.729 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.770 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.708 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.552 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.644 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.564 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.738 |
MOD_GlcNHglycan | 537 | 541 | PF01048 | 0.740 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.757 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.708 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.686 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.402 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.684 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.789 |
MOD_GlcNHglycan | 864 | 867 | PF01048 | 0.418 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.410 |
MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.769 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.814 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.743 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.552 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.777 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.763 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.768 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.638 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.705 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.632 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.671 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.608 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.562 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.497 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.717 |
MOD_N-GLC_1 | 1005 | 1010 | PF02516 | 0.504 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.558 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.602 |
MOD_N-GLC_1 | 970 | 975 | PF02516 | 0.594 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.692 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.618 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.563 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.335 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.661 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.526 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.635 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.516 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.351 |
MOD_PKA_1 | 511 | 517 | PF00069 | 0.616 |
MOD_PKA_2 | 1027 | 1033 | PF00069 | 0.749 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.739 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.696 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.477 |
MOD_PKA_2 | 940 | 946 | PF00069 | 0.521 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.564 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.335 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.726 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.612 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.624 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.641 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.551 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.611 |
MOD_Plk_4 | 950 | 956 | PF00069 | 0.543 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.719 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.808 |
MOD_ProDKin_1 | 953 | 959 | PF00069 | 0.390 |
MOD_SUMO_for_1 | 317 | 320 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 104 | 114 | PF00179 | 0.779 |
MOD_SUMO_rev_2 | 362 | 367 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 38 | 47 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 400 | 404 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 453 | 459 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 636 | 641 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 697 | 706 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 958 | 968 | PF00179 | 0.674 |
TRG_DiLeu_BaEn_1 | 455 | 460 | PF01217 | 0.493 |
TRG_DiLeu_BaEn_3 | 761 | 767 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_4 | 455 | 461 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_4 | 636 | 642 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_4 | 851 | 857 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_4 | 891 | 897 | PF01217 | 0.447 |
TRG_DiLeu_LyEn_5 | 455 | 460 | PF01217 | 0.467 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 853 | 856 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 878 | 881 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 923 | 925 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 928 | 930 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 944 | 946 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 998 | 1001 | PF00400 | 0.592 |
TRG_NLS_Bipartite_1 | 272 | 289 | PF00514 | 0.626 |
TRG_NLS_Bipartite_1 | 622 | 643 | PF00514 | 0.447 |
TRG_NLS_MonoExtC_3 | 391 | 396 | PF00514 | 0.691 |
TRG_NLS_MonoExtC_3 | 510 | 515 | PF00514 | 0.692 |
TRG_NLS_MonoExtC_3 | 775 | 780 | PF00514 | 0.753 |
TRG_NLS_MonoExtN_4 | 511 | 516 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 774 | 781 | PF00514 | 0.751 |
TRG_NLS_MonoExtN_4 | 990 | 997 | PF00514 | 0.757 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 974 | 978 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY8 | Leptomonas seymouri | 61% | 100% |
A0A1X0NGP0 | Trypanosomatidae | 39% | 100% |
A0A3R7NCJ6 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X904 | Leishmania donovani | 99% | 100% |
A4HFF6 | Leishmania braziliensis | 79% | 100% |
C9ZNK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AET3 | Leishmania major | 93% | 100% |
E9B5Y8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5ATL2 | Trypanosoma cruzi | 37% | 100% |