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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071204 | histone pre-mRNA 3'end processing complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HE27
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006398 | mRNA 3'-end processing by stem-loop binding and cleavage | 8 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008334 | histone mRNA metabolic process | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 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:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003729 | mRNA binding | 5 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0036002 | pre-mRNA binding | 5 | 1 |
GO:0071207 | histone pre-mRNA stem-loop binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.778 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.673 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.800 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.579 |
CLV_Separin_Metazoa | 266 | 270 | PF03568 | 0.591 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.696 |
DEG_SCF_FBW7_1 | 787 | 794 | PF00400 | 0.582 |
DOC_ANK_TNKS_1 | 17 | 24 | PF00023 | 0.556 |
DOC_ANK_TNKS_1 | 635 | 642 | PF00023 | 0.537 |
DOC_CKS1_1 | 10 | 15 | PF01111 | 0.579 |
DOC_CKS1_1 | 758 | 763 | PF01111 | 0.548 |
DOC_CKS1_1 | 819 | 824 | PF01111 | 0.730 |
DOC_CYCLIN_RxL_1 | 466 | 477 | PF00134 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.575 |
DOC_CYCLIN_yCln2_LP_2 | 497 | 503 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 823 | 829 | PF00134 | 0.558 |
DOC_MAPK_gen_1 | 168 | 179 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 217 | 224 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 269 | 277 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 410 | 416 | PF00069 | 0.735 |
DOC_MAPK_MEF2A_6 | 269 | 277 | PF00069 | 0.584 |
DOC_PP1_RVXF_1 | 173 | 180 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.621 |
DOC_PP2B_LxvP_1 | 552 | 555 | PF13499 | 0.677 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.575 |
DOC_PP4_MxPP_1 | 535 | 538 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 757 | 762 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 764 | 769 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 469 | 474 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 702 | 711 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 286 | 302 | PF00022 | 0.579 |
LIG_APCC_ABBA_1 | 26 | 31 | PF00400 | 0.537 |
LIG_BRCT_BRCA1_1 | 838 | 842 | PF00533 | 0.522 |
LIG_deltaCOP1_diTrp_1 | 663 | 669 | PF00928 | 0.505 |
LIG_EVH1_2 | 499 | 503 | PF00568 | 0.701 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.401 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.528 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.527 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.719 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.682 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.524 |
LIG_FHA_1 | 745 | 751 | PF00498 | 0.668 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.527 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.582 |
LIG_FHA_2 | 815 | 821 | PF00498 | 0.576 |
LIG_IRF3_LxIS_1 | 832 | 839 | PF10401 | 0.520 |
LIG_LIR_Apic_2 | 89 | 94 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 235 | 243 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 306 | 317 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 450 | 457 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 657 | 664 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 667 | 677 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 655 | 659 | PF02991 | 0.505 |
LIG_MYND_1 | 83 | 87 | PF01753 | 0.562 |
LIG_Pex14_1 | 665 | 669 | PF04695 | 0.506 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.640 |
LIG_SH2_GRB2like | 186 | 189 | PF00017 | 0.546 |
LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.504 |
LIG_SH3_2 | 412 | 417 | PF14604 | 0.579 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.556 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.546 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.715 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.690 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.625 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.687 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.579 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.516 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.518 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.466 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.709 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.591 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.625 |
LIG_SH3_3 | 824 | 830 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 491 | 498 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 785 | 790 | PF11976 | 0.538 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.585 |
LIG_WW_2 | 412 | 415 | PF00397 | 0.726 |
MOD_CDC14_SPxK_1 | 408 | 411 | PF00782 | 0.732 |
MOD_CDK_SPK_2 | 405 | 410 | PF00069 | 0.745 |
MOD_CDK_SPxK_1 | 405 | 411 | PF00069 | 0.729 |
MOD_CDK_SPxK_1 | 787 | 793 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 9 | 15 | PF00069 | 0.582 |
MOD_CDK_SPxxK_3 | 403 | 410 | PF00069 | 0.728 |
MOD_CDK_SPxxK_3 | 818 | 825 | PF00069 | 0.734 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.588 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.563 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.521 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.583 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.539 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.568 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.657 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.609 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.579 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.654 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.434 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.599 |
MOD_DYRK1A_RPxSP_1 | 732 | 736 | PF00069 | 0.558 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.734 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.678 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.346 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.600 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.681 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.637 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.722 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.618 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.674 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.552 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.621 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.732 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.544 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.588 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.680 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.490 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.618 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.554 |
MOD_GlcNHglycan | 753 | 757 | PF01048 | 0.556 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.591 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.605 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.546 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.626 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.619 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.587 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.530 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.623 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.560 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.593 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.517 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.618 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.540 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.587 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.711 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.234 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.563 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.538 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.568 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.538 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.692 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.703 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.778 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.621 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.531 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.531 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.537 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.685 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.532 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.552 |
MOD_NEK2_2 | 791 | 796 | PF00069 | 0.574 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.536 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.723 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.554 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.638 |
MOD_PIKK_1 | 654 | 660 | PF00454 | 0.665 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.530 |
MOD_PIKK_1 | 780 | 786 | PF00454 | 0.686 |
MOD_PIKK_1 | 814 | 820 | PF00454 | 0.595 |
MOD_PK_1 | 782 | 788 | PF00069 | 0.534 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.561 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.559 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.562 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.677 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.679 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.582 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.559 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.558 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.564 |
MOD_Plk_1 | 791 | 797 | PF00069 | 0.575 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.554 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.560 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.549 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.733 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.535 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.546 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.672 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.599 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.745 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.594 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.608 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.535 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.651 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.727 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.518 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.682 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.488 |
MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.584 |
MOD_ProDKin_1 | 757 | 763 | PF00069 | 0.549 |
MOD_ProDKin_1 | 764 | 770 | PF00069 | 0.515 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.680 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.705 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 194 | 199 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.700 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.733 |
TRG_NLS_MonoExtC_3 | 224 | 229 | PF00514 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF88 | Leishmania donovani | 63% | 99% |
A4I1D3 | Leishmania infantum | 62% | 99% |
E9AXH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 97% |
Q4QA02 | Leishmania major | 63% | 100% |