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: E9AUM8
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 | 520 | 524 | PF00656 | 0.739 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.864 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.763 |
CLV_PCSK_FUR_1 | 253 | 257 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.864 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 692 | 700 | PF00400 | 0.678 |
DEG_SCF_FBW7_1 | 747 | 754 | PF00400 | 0.835 |
DEG_SCF_TRCP1_1 | 93 | 98 | PF00400 | 0.556 |
DEG_SPOP_SBC_1 | 530 | 534 | PF00917 | 0.552 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.773 |
DOC_ANK_TNKS_1 | 838 | 845 | PF00023 | 0.674 |
DOC_CDC14_PxL_1 | 352 | 360 | PF14671 | 0.700 |
DOC_CDC14_PxL_1 | 586 | 594 | PF14671 | 0.683 |
DOC_CKS1_1 | 398 | 403 | PF01111 | 0.292 |
DOC_CKS1_1 | 566 | 571 | PF01111 | 0.707 |
DOC_CKS1_1 | 593 | 598 | PF01111 | 0.696 |
DOC_CKS1_1 | 678 | 683 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 602 | 613 | PF00134 | 0.719 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.299 |
DOC_MAPK_DCC_7 | 601 | 609 | PF00069 | 0.440 |
DOC_MAPK_FxFP_2 | 50 | 53 | PF00069 | 0.692 |
DOC_MAPK_gen_1 | 224 | 234 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 253 | 259 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 554 | 562 | PF00069 | 0.733 |
DOC_MAPK_MEF2A_6 | 227 | 236 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.302 |
DOC_PP1_RVXF_1 | 253 | 260 | PF00149 | 0.639 |
DOC_PP1_RVXF_1 | 30 | 36 | PF00149 | 0.779 |
DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.709 |
DOC_PP4_FxxP_1 | 421 | 424 | PF00568 | 0.777 |
DOC_PP4_FxxP_1 | 468 | 471 | PF00568 | 0.619 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.444 |
DOC_PP4_FxxP_1 | 566 | 569 | PF00568 | 0.708 |
DOC_PP4_FxxP_1 | 593 | 596 | PF00568 | 0.687 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.833 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 838 | 842 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.593 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 651 | 656 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 747 | 752 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 851 | 856 | PF00397 | 0.828 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 292 | 297 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 591 | 596 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 694 | 700 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 874 | 881 | PF00244 | 0.664 |
LIG_Actin_WH2_2 | 379 | 395 | PF00022 | 0.545 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.503 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.672 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.798 |
LIG_BRCT_BRCA1_1 | 625 | 629 | PF00533 | 0.700 |
LIG_CtBP_PxDLS_1 | 569 | 573 | PF00389 | 0.703 |
LIG_deltaCOP1_diTrp_1 | 871 | 875 | PF00928 | 0.451 |
LIG_EH1_1 | 179 | 187 | PF00400 | 0.488 |
LIG_eIF4E_1 | 636 | 642 | PF01652 | 0.594 |
LIG_EVH1_2 | 8 | 12 | PF00568 | 0.831 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.851 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.657 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.485 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.621 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.615 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.420 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.591 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.526 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.588 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.678 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.703 |
LIG_FHA_1 | 821 | 827 | PF00498 | 0.755 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.710 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.712 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.594 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.635 |
LIG_FHA_2 | 752 | 758 | PF00498 | 0.830 |
LIG_FHA_2 | 817 | 823 | PF00498 | 0.733 |
LIG_GBD_Chelix_1 | 339 | 347 | PF00786 | 0.546 |
LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.487 |
LIG_LIR_Apic_2 | 418 | 424 | PF02991 | 0.760 |
LIG_LIR_Apic_2 | 467 | 471 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.691 |
LIG_LIR_Apic_2 | 563 | 569 | PF02991 | 0.712 |
LIG_LIR_Apic_2 | 776 | 781 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 294 | 302 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 384 | 395 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 626 | 636 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 708 | 713 | PF02991 | 0.551 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.591 |
LIG_OCRL_FandH_1 | 343 | 355 | PF00620 | 0.595 |
LIG_Rb_pABgroove_1 | 381 | 389 | PF01858 | 0.433 |
LIG_Rb_pABgroove_1 | 483 | 491 | PF01858 | 0.805 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.659 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 89 | 93 | PF00017 | 0.748 |
LIG_SH2_PTP2 | 778 | 781 | PF00017 | 0.775 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.724 |
LIG_SH2_SRC | 89 | 92 | PF00017 | 0.747 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 862 | 866 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 282 | 285 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.775 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.850 |
LIG_SH3_1 | 584 | 590 | PF00018 | 0.683 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.665 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.501 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.814 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.299 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.721 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.683 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.647 |
LIG_SH3_3 | 649 | 655 | PF00018 | 0.693 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.696 |
LIG_SH3_3 | 714 | 720 | PF00018 | 0.784 |
LIG_SH3_3 | 828 | 834 | PF00018 | 0.745 |
LIG_SUMO_SIM_anti_2 | 170 | 176 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 374 | 380 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 567 | 573 | PF11976 | 0.699 |
LIG_SxIP_EBH_1 | 608 | 621 | PF03271 | 0.708 |
LIG_UBA3_1 | 222 | 228 | PF00899 | 0.485 |
LIG_UBA3_1 | 389 | 393 | PF00899 | 0.548 |
LIG_WRC_WIRS_1 | 881 | 886 | PF05994 | 0.492 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.813 |
MOD_CDK_SPxK_1 | 747 | 753 | PF00069 | 0.756 |
MOD_CDK_SPxxK_3 | 777 | 784 | PF00069 | 0.488 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.589 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.557 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.560 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.733 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.798 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.715 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.802 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.639 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.659 |
MOD_CK1_1 | 769 | 775 | PF00069 | 0.751 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.593 |
MOD_CK1_1 | 827 | 833 | PF00069 | 0.762 |
MOD_CK1_1 | 877 | 883 | PF00069 | 0.666 |
MOD_CK1_1 | 885 | 891 | PF00069 | 0.687 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.706 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.599 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.567 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.584 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.830 |
MOD_DYRK1A_RPxSP_1 | 4 | 8 | PF00069 | 0.772 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.707 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.735 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.705 |
MOD_GlcNHglycan | 507 | 511 | PF01048 | 0.823 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.740 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.781 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.623 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.760 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.808 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.683 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.749 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.723 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.739 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.553 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.714 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.666 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.736 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.753 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.572 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.583 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.574 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.648 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.756 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.828 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.704 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.728 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.708 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.391 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.820 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.601 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.625 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.791 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.714 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.654 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.737 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.776 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.566 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.587 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.678 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.673 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.580 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.807 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.801 |
MOD_N-GLC_2 | 795 | 797 | PF02516 | 0.645 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.575 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.686 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.650 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.602 |
MOD_PIKK_1 | 874 | 880 | PF00454 | 0.671 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.578 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.616 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.634 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.850 |
MOD_PKB_1 | 156 | 164 | PF00069 | 0.667 |
MOD_PKB_1 | 201 | 209 | PF00069 | 0.610 |
MOD_PKB_1 | 432 | 440 | PF00069 | 0.837 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.804 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.552 |
MOD_Plk_1 | 889 | 895 | PF00069 | 0.726 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.560 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.375 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.475 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.527 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.708 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.768 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.297 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.811 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.695 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.657 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.693 |
MOD_ProDKin_1 | 651 | 657 | PF00069 | 0.754 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.562 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.674 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.738 |
MOD_ProDKin_1 | 747 | 753 | PF00069 | 0.834 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.486 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.748 |
MOD_ProDKin_1 | 851 | 857 | PF00069 | 0.823 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.588 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 637 | 642 | PF01217 | 0.696 |
TRG_DiLeu_BaEn_1 | 691 | 696 | PF01217 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 605 | 610 | PF01217 | 0.707 |
TRG_DiLeu_LyEn_5 | 691 | 696 | PF01217 | 0.709 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.612 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 693 | 695 | PF00400 | 0.763 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEA0 | Leptomonas seymouri | 42% | 86% |
A0A3S7WW37 | Leishmania donovani | 89% | 100% |
A4HYT2 | Leishmania infantum | 90% | 100% |
E9AIE1 | Leishmania braziliensis | 76% | 100% |
Q4QCV6 | Leishmania major | 90% | 100% |