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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HYT2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004521 | RNA endonuclease activity | 5 | 7 |
GO:0004525 | ribonuclease III activity | 6 | 7 |
GO:0004540 | RNA nuclease activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 7 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 7 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0005488 | binding | 1 | 1 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 515 | 519 | PF00656 | 0.689 |
CLV_C14_Caspase3-7 | 814 | 818 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 870 | 872 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 250 | 254 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.798 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 869 | 871 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 250 | 256 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 862 | 866 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 687 | 695 | PF00400 | 0.586 |
DEG_APCC_DBOX_1 | 701 | 709 | PF00400 | 0.561 |
DEG_Kelch_Keap1_1 | 755 | 760 | PF01344 | 0.580 |
DEG_SCF_FBW7_1 | 742 | 749 | PF00400 | 0.774 |
DEG_SCF_TRCP1_1 | 528 | 533 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.730 |
DOC_ANK_TNKS_1 | 771 | 778 | PF00023 | 0.591 |
DOC_ANK_TNKS_1 | 833 | 840 | PF00023 | 0.641 |
DOC_CDC14_PxL_1 | 351 | 359 | PF14671 | 0.633 |
DOC_CDC14_PxL_1 | 581 | 589 | PF14671 | 0.600 |
DOC_CKS1_1 | 561 | 566 | PF01111 | 0.648 |
DOC_CKS1_1 | 588 | 593 | PF01111 | 0.642 |
DOC_CYCLIN_RxL_1 | 597 | 608 | PF00134 | 0.649 |
DOC_MAPK_FxFP_2 | 50 | 53 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 250 | 258 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 549 | 557 | PF00069 | 0.663 |
DOC_MAPK_MEF2A_6 | 226 | 235 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 252 | 259 | PF00149 | 0.569 |
DOC_PP1_RVXF_1 | 30 | 36 | PF00149 | 0.745 |
DOC_PP2B_LxvP_1 | 690 | 693 | PF13499 | 0.499 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.685 |
DOC_PP4_FxxP_1 | 420 | 423 | PF00568 | 0.724 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 561 | 564 | PF00568 | 0.689 |
DOC_PP4_FxxP_1 | 588 | 591 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 723 | 728 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 742 | 747 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 822 | 827 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 846 | 851 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 291 | 296 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 586 | 591 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 626 | 632 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 763 | 769 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 869 | 876 | PF00244 | 0.611 |
LIG_Actin_WH2_2 | 378 | 394 | PF00022 | 0.479 |
LIG_APCC_ABBA_1 | 278 | 283 | PF00400 | 0.416 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.635 |
LIG_BRCT_BRCA1_1 | 557 | 561 | PF00533 | 0.720 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.625 |
LIG_Clathr_ClatBox_1 | 691 | 695 | PF01394 | 0.527 |
LIG_CtBP_PxDLS_1 | 564 | 568 | PF00389 | 0.646 |
LIG_EH1_1 | 178 | 186 | PF00400 | 0.401 |
LIG_eIF4E_1 | 631 | 637 | PF01652 | 0.498 |
LIG_eIF4E_2 | 773 | 779 | PF01652 | 0.598 |
LIG_EVH1_2 | 8 | 12 | PF00568 | 0.774 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.779 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.627 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.403 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.532 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.543 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.234 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.527 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.608 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.610 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.611 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.645 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.621 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.548 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.773 |
LIG_FHA_2 | 812 | 818 | PF00498 | 0.663 |
LIG_GBD_Chelix_1 | 338 | 346 | PF00786 | 0.480 |
LIG_Integrin_isoDGR_2 | 761 | 763 | PF01839 | 0.594 |
LIG_LIR_Apic_2 | 190 | 196 | PF02991 | 0.395 |
LIG_LIR_Apic_2 | 417 | 423 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.641 |
LIG_LIR_Apic_2 | 558 | 564 | PF02991 | 0.704 |
LIG_LIR_Apic_2 | 771 | 776 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 293 | 301 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 621 | 631 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 630 | 634 | PF02991 | 0.558 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.523 |
LIG_OCRL_FandH_1 | 342 | 354 | PF00620 | 0.524 |
LIG_Rb_pABgroove_1 | 380 | 388 | PF01858 | 0.353 |
LIG_Rb_pABgroove_1 | 482 | 490 | PF01858 | 0.726 |
LIG_RPA_C_Fungi | 390 | 402 | PF08784 | 0.476 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.601 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 88 | 92 | PF00017 | 0.688 |
LIG_SH2_PTP2 | 773 | 776 | PF00017 | 0.700 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.636 |
LIG_SH2_SRC | 773 | 776 | PF00017 | 0.653 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.688 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 281 | 284 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.700 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.786 |
LIG_SH3_1 | 579 | 585 | PF00018 | 0.597 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.600 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.411 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.757 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.655 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.597 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.566 |
LIG_SH3_3 | 644 | 650 | PF00018 | 0.641 |
LIG_SH3_3 | 667 | 673 | PF00018 | 0.607 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.721 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.690 |
LIG_SUMO_SIM_anti_2 | 169 | 175 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 387 | 392 | PF11976 | 0.359 |
LIG_SUMO_SIM_anti_2 | 521 | 529 | PF11976 | 0.673 |
LIG_SUMO_SIM_par_1 | 373 | 379 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 562 | 568 | PF11976 | 0.643 |
LIG_SxIP_EBH_1 | 603 | 616 | PF03271 | 0.639 |
LIG_SxIP_EBH_1 | 643 | 657 | PF03271 | 0.516 |
LIG_TYR_ITIM | 629 | 634 | PF00017 | 0.451 |
LIG_UBA3_1 | 221 | 226 | PF00899 | 0.388 |
LIG_UBA3_1 | 388 | 392 | PF00899 | 0.479 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.749 |
MOD_CDK_SPK_2 | 846 | 851 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 742 | 748 | PF00069 | 0.710 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.507 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.511 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.535 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.647 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.757 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.739 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.560 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.597 |
MOD_CK1_1 | 764 | 770 | PF00069 | 0.692 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.699 |
MOD_CK1_1 | 872 | 878 | PF00069 | 0.612 |
MOD_CK1_1 | 880 | 886 | PF00069 | 0.620 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.651 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.604 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.767 |
MOD_DYRK1A_RPxSP_1 | 4 | 8 | PF00069 | 0.721 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.667 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.517 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.500 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.647 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.624 |
MOD_GlcNHglycan | 502 | 506 | PF01048 | 0.762 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.644 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.795 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.719 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.568 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.674 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.642 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.684 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.663 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.651 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.693 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.674 |
MOD_GlcNHglycan | 852 | 855 | PF01048 | 0.518 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.649 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.690 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.737 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.482 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.541 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.499 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.577 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.702 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.716 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.599 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.819 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.613 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.762 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.639 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.762 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.628 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.748 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.793 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.666 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.694 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.549 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.732 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.648 |
MOD_LATS_1 | 326 | 332 | PF00433 | 0.499 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.511 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.743 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.742 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.722 |
MOD_N-GLC_1 | 877 | 882 | PF02516 | 0.567 |
MOD_N-GLC_2 | 790 | 792 | PF02516 | 0.558 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.545 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.391 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.594 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.579 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.519 |
MOD_PIKK_1 | 869 | 875 | PF00454 | 0.644 |
MOD_PKA_1 | 869 | 875 | PF00069 | 0.572 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.535 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.549 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.564 |
MOD_PKA_2 | 833 | 839 | PF00069 | 0.783 |
MOD_PKA_2 | 869 | 875 | PF00069 | 0.651 |
MOD_PKB_1 | 155 | 163 | PF00069 | 0.601 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.540 |
MOD_PKB_1 | 431 | 439 | PF00069 | 0.767 |
MOD_PKB_1 | 869 | 877 | PF00069 | 0.617 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.739 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.690 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.506 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.306 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.419 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.641 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.692 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.745 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.601 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.626 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.642 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.693 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.597 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.647 |
MOD_ProDKin_1 | 742 | 748 | PF00069 | 0.773 |
MOD_ProDKin_1 | 822 | 828 | PF00069 | 0.688 |
MOD_ProDKin_1 | 846 | 852 | PF00069 | 0.752 |
TRG_DiLeu_BaEn_1 | 169 | 174 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_1 | 316 | 321 | PF01217 | 0.519 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.353 |
TRG_DiLeu_BaEn_1 | 632 | 637 | PF01217 | 0.618 |
TRG_DiLeu_BaEn_1 | 686 | 691 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 600 | 605 | PF01217 | 0.637 |
TRG_DiLeu_LyEn_5 | 686 | 691 | PF01217 | 0.639 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 416 | 419 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 688 | 690 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 868 | 871 | PF00400 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEA0 | Leptomonas seymouri | 42% | 86% |
A0A3S7WW37 | Leishmania donovani | 100% | 100% |
E9AIE1 | Leishmania braziliensis | 76% | 100% |
E9AUM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QCV6 | Leishmania major | 93% | 100% |