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: A0A3S5H829
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_NRD_NRD_1 | 217 | 219 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 896 | 898 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 896 | 898 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 835 | 837 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 622 | 628 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 838 | 842 | PF00082 | 0.546 |
CLV_Separin_Metazoa | 719 | 723 | PF03568 | 0.568 |
CLV_Separin_Metazoa | 766 | 770 | PF03568 | 0.675 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.592 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 835 | 843 | PF00400 | 0.560 |
DOC_CDC14_PxL_1 | 221 | 229 | PF14671 | 0.655 |
DOC_CDC14_PxL_1 | 6 | 14 | PF14671 | 0.489 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.572 |
DOC_CKS1_1 | 829 | 834 | PF01111 | 0.594 |
DOC_CYCLIN_RxL_1 | 180 | 191 | PF00134 | 0.616 |
DOC_CYCLIN_RxL_1 | 709 | 719 | PF00134 | 0.586 |
DOC_MAPK_FxFP_2 | 7 | 10 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 21 | 29 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 834 | 842 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 173 | 181 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 273 | 281 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 394 | 401 | PF00069 | 0.514 |
DOC_MAPK_NFAT4_5 | 370 | 378 | PF00069 | 0.490 |
DOC_MAPK_RevD_3 | 883 | 897 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 166 | 172 | PF00149 | 0.601 |
DOC_PP1_RVXF_1 | 24 | 30 | PF00149 | 0.467 |
DOC_PP1_RVXF_1 | 836 | 842 | PF00149 | 0.551 |
DOC_PP2B_LxvP_1 | 669 | 672 | PF13499 | 0.755 |
DOC_PP2B_LxvP_1 | 851 | 854 | PF13499 | 0.466 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.611 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.485 |
DOC_PP4_FxxP_1 | 877 | 880 | PF00568 | 0.582 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.773 |
DOC_USP7_UBL2_3 | 830 | 834 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 15 | 23 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 573 | 579 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 615 | 623 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 751 | 759 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 769 | 774 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 848 | 854 | PF00244 | 0.548 |
LIG_BIR_III_4 | 779 | 783 | PF00653 | 0.619 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 774 | 778 | PF00533 | 0.651 |
LIG_BRCT_BRCA1_1 | 873 | 877 | PF00533 | 0.522 |
LIG_Clathr_ClatBox_1 | 419 | 423 | PF01394 | 0.527 |
LIG_Clathr_ClatBox_1 | 839 | 843 | PF01394 | 0.552 |
LIG_CSL_BTD_1 | 825 | 828 | PF09270 | 0.693 |
LIG_deltaCOP1_diTrp_1 | 104 | 111 | PF00928 | 0.586 |
LIG_EVH1_2 | 795 | 799 | PF00568 | 0.524 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.544 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.561 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.462 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.505 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.501 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.578 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.714 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.596 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.602 |
LIG_LIR_Apic_2 | 874 | 880 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 732 | 738 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 865 | 871 | PF02991 | 0.540 |
LIG_LYPXL_S_1 | 8 | 12 | PF13949 | 0.480 |
LIG_LYPXL_yS_3 | 9 | 12 | PF13949 | 0.522 |
LIG_MLH1_MIPbox_1 | 774 | 778 | PF16413 | 0.656 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.449 |
LIG_NRBOX | 84 | 90 | PF00104 | 0.494 |
LIG_NRBOX | 866 | 872 | PF00104 | 0.608 |
LIG_Pex14_1 | 773 | 777 | PF04695 | 0.614 |
LIG_Rb_LxCxE_1 | 311 | 331 | PF01857 | 0.609 |
LIG_RPA_C_Fungi | 252 | 264 | PF08784 | 0.542 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 644 | 648 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.710 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.516 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.571 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 371 | 377 | PF11976 | 0.238 |
LIG_SUMO_SIM_anti_2 | 87 | 94 | PF11976 | 0.577 |
LIG_SUMO_SIM_anti_2 | 879 | 886 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 467 | 472 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 694 | 700 | PF11976 | 0.632 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.604 |
LIG_TRFH_1 | 6 | 10 | PF08558 | 0.523 |
MOD_CDK_SPxK_1 | 828 | 834 | PF00069 | 0.607 |
MOD_CDK_SPxxK_3 | 828 | 835 | PF00069 | 0.601 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.519 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.601 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.436 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.484 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.621 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.662 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.699 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.754 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.644 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.622 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.701 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.434 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.742 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.368 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.596 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.452 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.630 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.243 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.682 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.561 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.541 |
MOD_GlcNHglycan | 104 | 109 | PF01048 | 0.525 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.558 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.694 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.482 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.652 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.354 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.644 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.455 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.564 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.426 |
MOD_GlcNHglycan | 527 | 531 | PF01048 | 0.548 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.734 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.651 |
MOD_GlcNHglycan | 608 | 612 | PF01048 | 0.633 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.694 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.583 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.527 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.710 |
MOD_GlcNHglycan | 799 | 802 | PF01048 | 0.707 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.652 |
MOD_GlcNHglycan | 874 | 877 | PF01048 | 0.494 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.518 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.491 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.560 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.540 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.510 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.548 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.605 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.536 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.502 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.622 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.699 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.673 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.700 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.480 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.726 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.576 |
MOD_LATS_1 | 571 | 577 | PF00433 | 0.766 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.555 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.505 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.578 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.641 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.553 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.578 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.733 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.616 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.688 |
MOD_NEK2_1 | 871 | 876 | PF00069 | 0.533 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.499 |
MOD_NEK2_2 | 687 | 692 | PF00069 | 0.683 |
MOD_NEK2_2 | 773 | 778 | PF00069 | 0.615 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.565 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.605 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.563 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.553 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.778 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.789 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.753 |
MOD_PIKK_1 | 883 | 889 | PF00454 | 0.594 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.486 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.425 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.664 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.658 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.676 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.718 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.622 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.549 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.774 |
MOD_PKA_2 | 849 | 855 | PF00069 | 0.603 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.746 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.597 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.622 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.534 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.524 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.615 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.596 |
MOD_Plk_4 | 773 | 779 | PF00069 | 0.658 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.543 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.511 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.681 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.607 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.530 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_1 | 415 | 420 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 716 | 721 | PF01217 | 0.477 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 890 | 895 | PF01217 | 0.615 |
TRG_DiLeu_BaEn_4 | 890 | 896 | PF01217 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.711 |
TRG_DiLeu_BaLyEn_6 | 483 | 488 | PF01217 | 0.629 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 625 | 627 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 836 | 839 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 845 | 848 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 895 | 897 | PF00400 | 0.551 |
TRG_NLS_MonoExtC_3 | 833 | 838 | PF00514 | 0.575 |
TRG_NLS_MonoExtN_4 | 832 | 839 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 712 | 716 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P797 | Leptomonas seymouri | 46% | 100% |
A0A1X0NKL2 | Trypanosomatidae | 25% | 100% |
A0A3R7LZS8 | Trypanosoma rangeli | 27% | 100% |
A4HPF6 | Leishmania braziliensis | 75% | 100% |
A4ID78 | Leishmania infantum | 99% | 100% |
E9AT68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1C9 | Leishmania major | 89% | 100% |
V5B0C2 | Trypanosoma cruzi | 26% | 100% |