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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A0A3S7WTI6
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 6 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009451 | RNA modification | 5 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 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:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000455 | enzyme-directed rRNA pseudouridine synthesis | 8 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031118 | rRNA pseudouridine synthesis | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0009982 | pseudouridine synthase activity | 4 | 6 |
GO:0016853 | isomerase activity | 2 | 6 |
GO:0016866 | intramolecular transferase activity | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 852 | 854 | PF00675 | 0.380 |
CLV_PCSK_FUR_1 | 212 | 216 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 807 | 809 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 852 | 854 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 553 | 555 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 807 | 809 | PF00082 | 0.691 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.509 |
CLV_PCSK_PC7_1 | 470 | 476 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.846 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 810 | 814 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 862 | 866 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.498 |
CLV_Separin_Metazoa | 363 | 367 | PF03568 | 0.426 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 685 | 693 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 894 | 902 | PF00400 | 0.542 |
DEG_SCF_FBW7_1 | 941 | 948 | PF00400 | 0.702 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.664 |
DEG_SPOP_SBC_1 | 671 | 675 | PF00917 | 0.576 |
DOC_CKS1_1 | 701 | 706 | PF01111 | 0.513 |
DOC_CKS1_1 | 942 | 947 | PF01111 | 0.706 |
DOC_CYCLIN_RxL_1 | 297 | 306 | PF00134 | 0.594 |
DOC_CYCLIN_RxL_1 | 508 | 517 | PF00134 | 0.587 |
DOC_CYCLIN_RxL_1 | 84 | 94 | PF00134 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 901 | 907 | PF00134 | 0.495 |
DOC_MAPK_gen_1 | 862 | 870 | PF00069 | 0.513 |
DOC_MAPK_HePTP_8 | 459 | 473 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 732 | 741 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 890 | 898 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 90 | 97 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 910 | 918 | PF00069 | 0.301 |
DOC_MAPK_NFAT4_5 | 90 | 98 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 278 | 285 | PF00149 | 0.523 |
DOC_PP1_RVXF_1 | 63 | 70 | PF00149 | 0.572 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.649 |
DOC_PP2B_LxvP_1 | 668 | 671 | PF13499 | 0.783 |
DOC_PP2B_LxvP_1 | 715 | 718 | PF13499 | 0.740 |
DOC_PP4_FxxP_1 | 172 | 175 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 1024 | 1028 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 945 | 949 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 962 | 966 | PF00917 | 0.627 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 795 | 800 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 941 | 946 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 710 | 718 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 732 | 740 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 784 | 789 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 862 | 871 | PF00244 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.610 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.610 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.610 |
LIG_BIR_III_4 | 719 | 723 | PF00653 | 0.696 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.637 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.500 |
LIG_BRCT_BRCA1_1 | 983 | 987 | PF00533 | 0.633 |
LIG_Clathr_ClatBox_1 | 1018 | 1022 | PF01394 | 0.637 |
LIG_deltaCOP1_diTrp_1 | 274 | 278 | PF00928 | 0.548 |
LIG_deltaCOP1_diTrp_1 | 505 | 514 | PF00928 | 0.670 |
LIG_eIF4E_1 | 1013 | 1019 | PF01652 | 0.643 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.561 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.504 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.697 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.676 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.607 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.572 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.542 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.513 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.786 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.651 |
LIG_LIR_Apic_2 | 169 | 175 | PF02991 | 0.579 |
LIG_LIR_Apic_2 | 439 | 445 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 753 | 758 | PF02991 | 0.553 |
LIG_LIR_Apic_2 | 76 | 82 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 505 | 515 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 908 | 918 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 99 | 105 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 908 | 914 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.601 |
LIG_MYND_1 | 374 | 378 | PF01753 | 0.490 |
LIG_PCNA_TLS_4 | 90 | 97 | PF02747 | 0.500 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.540 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.676 |
LIG_SH2_CRK | 456 | 460 | PF00017 | 0.511 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 1009 | 1013 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 873 | 877 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 911 | 914 | PF00017 | 0.619 |
LIG_SH2_SRC | 1013 | 1016 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 1009 | 1013 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.695 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 1009 | 1012 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 857 | 860 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 911 | 914 | PF00017 | 0.521 |
LIG_SH3_3 | 1018 | 1024 | PF00018 | 0.540 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.653 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.697 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.616 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.552 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.632 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.842 |
LIG_SH3_3 | 663 | 669 | PF00018 | 0.712 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.488 |
LIG_SH3_3 | 939 | 945 | PF00018 | 0.689 |
LIG_SUMO_SIM_par_1 | 1017 | 1022 | PF11976 | 0.638 |
LIG_TRAF2_1 | 529 | 532 | PF00917 | 0.754 |
LIG_WW_1 | 592 | 595 | PF00397 | 0.663 |
LIG_WW_2 | 666 | 669 | PF00397 | 0.599 |
MOD_CDK_SPxxK_3 | 473 | 480 | PF00069 | 0.627 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.685 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.666 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.655 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.728 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.660 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.504 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.701 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.667 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.776 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.686 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.639 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.590 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.600 |
MOD_CK1_1 | 863 | 869 | PF00069 | 0.459 |
MOD_CK1_1 | 948 | 954 | PF00069 | 0.645 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.587 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.479 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.813 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.744 |
MOD_CMANNOS | 275 | 278 | PF00535 | 0.526 |
MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.510 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.705 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.788 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.642 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.775 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.615 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.756 |
MOD_GlcNHglycan | 267 | 271 | PF01048 | 0.745 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.711 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.657 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.635 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.686 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.565 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.622 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.757 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.633 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.590 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.664 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.483 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.806 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.769 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.777 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.746 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.742 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.682 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.342 |
MOD_GlcNHglycan | 931 | 934 | PF01048 | 0.679 |
MOD_GlcNHglycan | 969 | 972 | PF01048 | 0.746 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.697 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.691 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.724 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.498 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.590 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.707 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.734 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.591 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.604 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.603 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.750 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.553 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.666 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.527 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.685 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.602 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.717 |
MOD_GSK3_1 | 929 | 936 | PF00069 | 0.698 |
MOD_GSK3_1 | 941 | 948 | PF00069 | 0.667 |
MOD_N-GLC_1 | 630 | 635 | PF02516 | 0.639 |
MOD_N-GLC_1 | 654 | 659 | PF02516 | 0.593 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.657 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.583 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.447 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.712 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.563 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.580 |
MOD_NEK2_1 | 955 | 960 | PF00069 | 0.596 |
MOD_NEK2_1 | 987 | 992 | PF00069 | 0.565 |
MOD_NEK2_2 | 335 | 340 | PF00069 | 0.491 |
MOD_NEK2_2 | 593 | 598 | PF00069 | 0.603 |
MOD_NEK2_2 | 857 | 862 | PF00069 | 0.542 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.747 |
MOD_PK_1 | 412 | 418 | PF00069 | 0.506 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.566 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.506 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.717 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.557 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.559 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.643 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.712 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.608 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.779 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.485 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.568 |
MOD_PKA_2 | 840 | 846 | PF00069 | 0.697 |
MOD_PKB_1 | 228 | 236 | PF00069 | 0.734 |
MOD_PKB_1 | 516 | 524 | PF00069 | 0.775 |
MOD_PKB_1 | 808 | 816 | PF00069 | 0.677 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.634 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.602 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.704 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.420 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.644 |
MOD_Plk_1 | 877 | 883 | PF00069 | 0.542 |
MOD_Plk_1 | 948 | 954 | PF00069 | 0.598 |
MOD_Plk_2-3 | 1017 | 1023 | PF00069 | 0.635 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.697 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.692 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.452 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.504 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.628 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.530 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.510 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.592 |
MOD_Plk_4 | 877 | 883 | PF00069 | 0.595 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.600 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.658 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.620 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.553 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.593 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.659 |
MOD_ProDKin_1 | 795 | 801 | PF00069 | 0.666 |
MOD_ProDKin_1 | 941 | 947 | PF00069 | 0.672 |
MOD_SUMO_rev_2 | 637 | 647 | PF00179 | 0.587 |
TRG_DiLeu_BaEn_1 | 293 | 298 | PF01217 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.755 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.691 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 911 | 914 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 852 | 854 | PF00400 | 0.580 |
TRG_NLS_MonoExtN_4 | 805 | 811 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 16 | 21 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 919 | 924 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P442 | Leptomonas seymouri | 43% | 100% |
A4H810 | Leishmania braziliensis | 66% | 98% |
E9AQ38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QFE4 | Leishmania major | 87% | 100% |