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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AF65
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 5 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009056 | catabolic process | 2 | 5 |
GO:0009057 | macromolecule catabolic process | 4 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016579 | protein deubiquitination | 6 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044248 | cellular catabolic process | 3 | 5 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 5 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 5 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 5 |
GO:0070646 | protein modification by small protein removal | 5 | 5 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:1901575 | organic substance catabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004175 | endopeptidase activity | 4 | 2 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 2 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 5 |
GO:0008233 | peptidase activity | 3 | 5 |
GO:0008234 | cysteine-type peptidase activity | 4 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 5 |
GO:0101005 | deubiquitinase activity | 5 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.316 |
CLV_C14_Caspase3-7 | 916 | 920 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.831 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 795 | 797 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 829 | 831 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.573 |
CLV_PCSK_FUR_1 | 23 | 27 | PF00082 | 0.628 |
CLV_PCSK_FUR_1 | 716 | 720 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.831 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 829 | 831 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 861 | 863 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 718 | 720 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 736 | 738 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 861 | 863 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 877 | 881 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 890 | 894 | PF00082 | 0.370 |
CLV_Separin_Metazoa | 687 | 691 | PF03568 | 0.526 |
DEG_COP1_1 | 437 | 445 | PF00400 | 0.598 |
DEG_SPOP_SBC_1 | 202 | 206 | PF00917 | 0.675 |
DEG_SPOP_SBC_1 | 521 | 525 | PF00917 | 0.526 |
DOC_CDC14_PxL_1 | 345 | 353 | PF14671 | 0.711 |
DOC_CKS1_1 | 475 | 480 | PF01111 | 0.412 |
DOC_CYCLIN_RxL_1 | 230 | 241 | PF00134 | 0.613 |
DOC_CYCLIN_RxL_1 | 422 | 432 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 701 | 707 | PF00134 | 0.388 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.526 |
DOC_MAPK_RevD_3 | 898 | 914 | PF00069 | 0.554 |
DOC_PP1_RVXF_1 | 604 | 611 | PF00149 | 0.433 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.599 |
DOC_SPAK_OSR1_1 | 642 | 646 | PF12202 | 0.433 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 672 | 676 | PF12436 | 0.396 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.814 |
DOC_WW_Pin1_4 | 856 | 861 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 498 | 507 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 606 | 611 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 719 | 725 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 772 | 780 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 852 | 860 | PF00244 | 0.691 |
LIG_Actin_WH2_2 | 801 | 816 | PF00022 | 0.562 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.758 |
LIG_BRCT_BRCA1_1 | 639 | 643 | PF00533 | 0.526 |
LIG_eIF4E_1 | 641 | 647 | PF01652 | 0.433 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.588 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.680 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.475 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.454 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.692 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.532 |
LIG_FHA_1 | 745 | 751 | PF00498 | 0.334 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.749 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.688 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.705 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.489 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.437 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.349 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.260 |
LIG_FHA_2 | 814 | 820 | PF00498 | 0.650 |
LIG_FHA_2 | 894 | 900 | PF00498 | 0.455 |
LIG_HP1_1 | 729 | 733 | PF01393 | 0.316 |
LIG_Integrin_isoDGR_2 | 863 | 865 | PF01839 | 0.742 |
LIG_IRF3_LxIS_1 | 643 | 650 | PF10401 | 0.526 |
LIG_LIR_Apic_2 | 174 | 179 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 723 | 729 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 640 | 651 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 781 | 788 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 906 | 915 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 725 | 730 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 806 | 812 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 906 | 911 | PF02991 | 0.526 |
LIG_NRBOX | 569 | 575 | PF00104 | 0.526 |
LIG_PCNA_yPIPBox_3 | 468 | 482 | PF02747 | 0.480 |
LIG_PDZ_Class_1 | 918 | 923 | PF00595 | 0.617 |
LIG_Pex14_2 | 751 | 755 | PF04695 | 0.526 |
LIG_REV1ctd_RIR_1 | 691 | 701 | PF16727 | 0.526 |
LIG_SH2_CRK | 783 | 787 | PF00017 | 0.480 |
LIG_SH2_CRK | 809 | 813 | PF00017 | 0.509 |
LIG_SH2_GRB2like | 466 | 469 | PF00017 | 0.526 |
LIG_SH2_SRC | 466 | 469 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 604 | 608 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 753 | 756 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 885 | 888 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 908 | 911 | PF00017 | 0.524 |
LIG_SH3_1 | 406 | 412 | PF00018 | 0.698 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.652 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.659 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.744 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.667 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.594 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.526 |
LIG_SH3_4 | 585 | 592 | PF00018 | 0.386 |
LIG_SUMO_SIM_anti_2 | 896 | 902 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 523 | 531 | PF11976 | 0.526 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.654 |
LIG_TYR_ITIM | 910 | 915 | PF00017 | 0.550 |
LIG_TYR_ITSM | 779 | 786 | PF00017 | 0.526 |
LIG_UBA3_1 | 543 | 548 | PF00899 | 0.501 |
LIG_UBA3_1 | 570 | 579 | PF00899 | 0.526 |
LIG_WRC_WIRS_1 | 391 | 396 | PF05994 | 0.729 |
LIG_WW_2 | 307 | 310 | PF00397 | 0.606 |
LIG_WW_3 | 276 | 280 | PF00397 | 0.606 |
MOD_CDC14_SPxK_1 | 859 | 862 | PF00782 | 0.628 |
MOD_CDK_SPK_2 | 675 | 680 | PF00069 | 0.316 |
MOD_CDK_SPK_2 | 81 | 86 | PF00069 | 0.686 |
MOD_CDK_SPK_2 | 856 | 861 | PF00069 | 0.623 |
MOD_CDK_SPxK_1 | 856 | 862 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.629 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.621 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.695 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.817 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.742 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.814 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.609 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.685 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.674 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.752 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.749 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.676 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.689 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.688 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.450 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.433 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.681 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.705 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.709 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.749 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.618 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.705 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.526 |
MOD_CK2_1 | 661 | 667 | PF00069 | 0.392 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.260 |
MOD_CMANNOS | 607 | 610 | PF00535 | 0.433 |
MOD_Cter_Amidation | 496 | 499 | PF01082 | 0.419 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.739 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.623 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.710 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.639 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.738 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.818 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.779 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.715 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.778 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.548 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.718 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.763 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.512 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.728 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.756 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.730 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.789 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.671 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.674 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.682 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.747 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.725 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.633 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.699 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.712 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.758 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.693 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.667 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.616 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.377 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.399 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.321 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.671 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.433 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.711 |
MOD_GSK3_1 | 871 | 878 | PF00069 | 0.780 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.673 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.733 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.743 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.524 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.686 |
MOD_N-GLC_1 | 890 | 895 | PF02516 | 0.516 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.758 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.634 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.663 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.740 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.637 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.356 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.388 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.526 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.399 |
MOD_NEK2_1 | 813 | 818 | PF00069 | 0.622 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.641 |
MOD_OFUCOSY | 629 | 636 | PF10250 | 0.433 |
MOD_OFUCOSY | 769 | 775 | PF10250 | 0.386 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.742 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.768 |
MOD_PIKK_1 | 656 | 662 | PF00454 | 0.442 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.758 |
MOD_PKA_1 | 43 | 49 | PF00069 | 0.708 |
MOD_PKA_1 | 498 | 504 | PF00069 | 0.414 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.615 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.690 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.707 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.776 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.642 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.439 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.712 |
MOD_PKA_2 | 771 | 777 | PF00069 | 0.526 |
MOD_PKA_2 | 851 | 857 | PF00069 | 0.708 |
MOD_PKB_1 | 24 | 32 | PF00069 | 0.689 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.711 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.687 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.524 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.433 |
MOD_Plk_1 | 744 | 750 | PF00069 | 0.480 |
MOD_Plk_1 | 893 | 899 | PF00069 | 0.410 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.613 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.635 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.480 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.406 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.709 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.484 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.421 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.433 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.743 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.576 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.732 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.744 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.687 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.412 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.567 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.316 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.779 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.812 |
MOD_ProDKin_1 | 856 | 862 | PF00069 | 0.599 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.665 |
MOD_SUMO_for_1 | 743 | 746 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 511 | 521 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 594 | 601 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 665 | 673 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 789 | 794 | PF00179 | 0.659 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.627 |
TRG_DiLeu_BaLyEn_6 | 808 | 813 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 783 | 786 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 809 | 812 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 908 | 911 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 912 | 915 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.821 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 488 | 491 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 655 | 658 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 828 | 830 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 912 | 914 | PF00400 | 0.558 |
TRG_NLS_MonoExtC_3 | 795 | 800 | PF00514 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 403 | 408 | PF00026 | 0.735 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X9D2 | Leishmania donovani | 81% | 100% |
A4HMR5 | Leishmania braziliensis | 45% | 96% |
E9B6C1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |