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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4ID78
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0032392 | DNA geometric change | 7 | 3 |
GO:0032508 | DNA duplex unwinding | 8 | 3 |
GO:0051276 | chromosome organization | 5 | 3 |
GO:0071103 | DNA conformation change | 6 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 3 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003677 | DNA binding | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 895 | 897 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 625 | 627 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 834 | 836 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 895 | 897 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 834 | 836 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 621 | 627 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 837 | 841 | PF00082 | 0.497 |
CLV_Separin_Metazoa | 718 | 722 | PF03568 | 0.464 |
CLV_Separin_Metazoa | 765 | 769 | PF03568 | 0.564 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 834 | 842 | PF00400 | 0.512 |
DOC_CDC14_PxL_1 | 221 | 229 | PF14671 | 0.529 |
DOC_CDC14_PxL_1 | 6 | 14 | PF14671 | 0.445 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.502 |
DOC_CKS1_1 | 828 | 833 | PF01111 | 0.512 |
DOC_CYCLIN_RxL_1 | 180 | 191 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 708 | 718 | PF00134 | 0.518 |
DOC_MAPK_FxFP_2 | 7 | 10 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 21 | 29 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 833 | 841 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 173 | 181 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 273 | 281 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 394 | 401 | PF00069 | 0.468 |
DOC_MAPK_NFAT4_5 | 370 | 378 | PF00069 | 0.444 |
DOC_MAPK_RevD_3 | 882 | 896 | PF00069 | 0.415 |
DOC_PP1_RVXF_1 | 166 | 172 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 24 | 30 | PF00149 | 0.415 |
DOC_PP1_RVXF_1 | 835 | 841 | PF00149 | 0.505 |
DOC_PP2B_LxvP_1 | 668 | 671 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 850 | 853 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 876 | 879 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 757 | 761 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.753 |
DOC_USP7_UBL2_3 | 829 | 833 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 15 | 23 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 572 | 578 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 614 | 622 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 750 | 758 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 768 | 773 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 847 | 853 | PF00244 | 0.486 |
LIG_BIR_III_4 | 778 | 782 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 773 | 777 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 872 | 876 | PF00533 | 0.471 |
LIG_Clathr_ClatBox_1 | 419 | 423 | PF01394 | 0.457 |
LIG_Clathr_ClatBox_1 | 838 | 842 | PF01394 | 0.503 |
LIG_CSL_BTD_1 | 824 | 827 | PF09270 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 104 | 111 | PF00928 | 0.535 |
LIG_EVH1_2 | 794 | 798 | PF00568 | 0.485 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.479 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.494 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.393 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.498 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.481 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.350 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.490 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.513 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.548 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 873 | 879 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 731 | 737 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 864 | 870 | PF02991 | 0.483 |
LIG_LYPXL_S_1 | 8 | 12 | PF13949 | 0.442 |
LIG_LYPXL_yS_3 | 9 | 12 | PF13949 | 0.466 |
LIG_MLH1_MIPbox_1 | 773 | 777 | PF16413 | 0.549 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.371 |
LIG_NRBOX | 84 | 90 | PF00104 | 0.415 |
LIG_NRBOX | 865 | 871 | PF00104 | 0.419 |
LIG_Pex14_1 | 772 | 776 | PF04695 | 0.524 |
LIG_Rb_LxCxE_1 | 311 | 331 | PF01857 | 0.493 |
LIG_RPA_C_Fungi | 252 | 264 | PF08784 | 0.425 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 643 | 647 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.551 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.454 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.509 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 371 | 377 | PF11976 | 0.212 |
LIG_SUMO_SIM_anti_2 | 87 | 94 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 878 | 885 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 467 | 472 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 693 | 699 | PF11976 | 0.568 |
LIG_TRAF2_1 | 524 | 527 | PF00917 | 0.537 |
LIG_TRFH_1 | 6 | 10 | PF08558 | 0.468 |
MOD_CDK_SPxK_1 | 827 | 833 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 827 | 834 | PF00069 | 0.518 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.485 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.558 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.562 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.451 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.564 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.579 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.573 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.652 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.583 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.540 |
MOD_CK1_1 | 752 | 758 | PF00069 | 0.661 |
MOD_CK1_1 | 771 | 777 | PF00069 | 0.534 |
MOD_CK1_1 | 796 | 802 | PF00069 | 0.732 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.439 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.536 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.394 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.207 |
MOD_CK2_1 | 814 | 820 | PF00069 | 0.581 |
MOD_CK2_1 | 858 | 864 | PF00069 | 0.527 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.484 |
MOD_GlcNHglycan | 104 | 109 | PF01048 | 0.489 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.521 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.648 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.391 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.672 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.291 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.614 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.497 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.592 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.534 |
MOD_GlcNHglycan | 526 | 530 | PF01048 | 0.556 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.661 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.646 |
MOD_GlcNHglycan | 607 | 611 | PF01048 | 0.518 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.615 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.588 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.492 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.680 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.641 |
MOD_GlcNHglycan | 850 | 853 | PF01048 | 0.613 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.436 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.501 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.417 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.492 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.469 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.480 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.526 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.497 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.556 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.590 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.649 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.702 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.651 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.494 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.593 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.538 |
MOD_LATS_1 | 570 | 576 | PF00433 | 0.607 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.487 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.469 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.510 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.628 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.586 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.535 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.651 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.535 |
MOD_NEK2_1 | 767 | 772 | PF00069 | 0.624 |
MOD_NEK2_1 | 870 | 875 | PF00069 | 0.522 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.445 |
MOD_NEK2_2 | 686 | 691 | PF00069 | 0.649 |
MOD_NEK2_2 | 772 | 777 | PF00069 | 0.525 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.548 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.548 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.454 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.473 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.697 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.671 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.576 |
MOD_PIKK_1 | 882 | 888 | PF00454 | 0.580 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.411 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.415 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.539 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.582 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.598 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.652 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.544 |
MOD_PKA_2 | 767 | 773 | PF00069 | 0.488 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.627 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.550 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.716 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.540 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.559 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.470 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.496 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.580 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.505 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.624 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.534 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.467 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.643 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.525 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.478 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.256 |
TRG_DiLeu_BaEn_1 | 415 | 420 | PF01217 | 0.426 |
TRG_DiLeu_BaEn_1 | 715 | 720 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_1 | 889 | 894 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_4 | 889 | 895 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 483 | 488 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 604 | 606 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 709 | 712 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 835 | 838 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 844 | 847 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 894 | 896 | PF00400 | 0.485 |
TRG_NLS_MonoExtC_3 | 832 | 837 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 831 | 838 | PF00514 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 711 | 715 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P797 | Leptomonas seymouri | 46% | 100% |
A0A1X0NKL2 | Trypanosomatidae | 25% | 100% |
A0A3R7LZS8 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H829 | Leishmania donovani | 99% | 100% |
A4HPF6 | Leishmania braziliensis | 75% | 100% |
E9AT68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1C9 | Leishmania major | 90% | 100% |
V5B0C2 | Trypanosoma cruzi | 26% | 100% |