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: E9AMP3
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0007096 | regulation of exit from mitosis | 7 | 7 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 7 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032465 | regulation of cytokinesis | 5 | 1 |
GO:0032467 | positive regulation of cytokinesis | 6 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0051302 | regulation of cell division | 4 | 1 |
GO:0051781 | positive regulation of cell division | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 672 | 678 | PF00089 | 0.634 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 835 | 837 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 950 | 952 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 834 | 836 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 853 | 855 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 950 | 952 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 721 | 723 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 853 | 855 | PF00082 | 0.706 |
CLV_PCSK_PC7_1 | 410 | 416 | PF00082 | 0.516 |
CLV_PCSK_PC7_1 | 849 | 855 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 985 | 989 | PF00082 | 0.699 |
CLV_Separin_Metazoa | 760 | 764 | PF03568 | 0.574 |
CLV_Separin_Metazoa | 83 | 87 | PF03568 | 0.446 |
DEG_APCC_KENBOX_2 | 13 | 17 | PF00400 | 0.399 |
DEG_SCF_TRCP1_1 | 107 | 112 | PF00400 | 0.486 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.507 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.643 |
DEG_SPOP_SBC_1 | 537 | 541 | PF00917 | 0.613 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.391 |
DOC_CKS1_1 | 934 | 939 | PF01111 | 0.600 |
DOC_CYCLIN_yCln2_LP_2 | 58 | 64 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 282 | 291 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 495 | 505 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.498 |
DOC_MAPK_HePTP_8 | 279 | 291 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 450 | 459 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 498 | 507 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 900 | 906 | PF00149 | 0.665 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 973 | 976 | PF13499 | 0.648 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 727 | 731 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 842 | 846 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 864 | 868 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 943 | 947 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 976 | 980 | PF00917 | 0.734 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 875 | 880 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 933 | 938 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 962 | 967 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 169 | 176 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 375 | 383 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 531 | 537 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 590 | 598 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 674 | 684 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 713 | 720 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 793 | 801 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 835 | 844 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 945 | 949 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 970 | 974 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 292 | 309 | PF00022 | 0.448 |
LIG_Actin_WH2_2 | 646 | 664 | PF00022 | 0.473 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.424 |
LIG_BIR_III_2 | 607 | 611 | PF00653 | 0.602 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 748 | 752 | PF00533 | 0.594 |
LIG_CtBP_PxDLS_1 | 68 | 72 | PF00389 | 0.327 |
LIG_deltaCOP1_diTrp_1 | 190 | 196 | PF00928 | 0.400 |
LIG_deltaCOP1_diTrp_1 | 253 | 262 | PF00928 | 0.357 |
LIG_eIF4E_1 | 300 | 306 | PF01652 | 0.446 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.472 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.340 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.478 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.529 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.518 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.397 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.537 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.659 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.618 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.514 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.674 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.600 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.657 |
LIG_FHA_1 | 827 | 833 | PF00498 | 0.672 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.552 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.654 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.474 |
LIG_FHA_2 | 916 | 922 | PF00498 | 0.525 |
LIG_FHA_2 | 954 | 960 | PF00498 | 0.670 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.356 |
LIG_Integrin_RGD_1 | 625 | 627 | PF01839 | 0.523 |
LIG_Integrin_RGD_1 | 875 | 877 | PF01839 | 0.539 |
LIG_LIR_Apic_2 | 240 | 244 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 45 | 56 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 648 | 654 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 749 | 758 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 648 | 652 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.360 |
LIG_LYPXL_S_1 | 199 | 203 | PF13949 | 0.275 |
LIG_MLH1_MIPbox_1 | 748 | 752 | PF16413 | 0.594 |
LIG_MYND_1 | 381 | 385 | PF01753 | 0.546 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.352 |
LIG_PAM2_1 | 736 | 748 | PF00658 | 0.513 |
LIG_PCNA_PIPBox_1 | 5 | 14 | PF02747 | 0.471 |
LIG_Pex14_1 | 192 | 196 | PF04695 | 0.475 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.346 |
LIG_PTAP_UEV_1 | 939 | 944 | PF05743 | 0.656 |
LIG_SH2_NCK_1 | 838 | 842 | PF00017 | 0.647 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.395 |
LIG_SH2_SRC | 489 | 492 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 747 | 751 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 838 | 842 | PF00017 | 0.695 |
LIG_SH2_STAP1 | 851 | 855 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 751 | 754 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.816 |
LIG_SH3_1 | 574 | 580 | PF00018 | 0.502 |
LIG_SH3_2 | 940 | 945 | PF14604 | 0.669 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.453 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.635 |
LIG_SH3_3 | 888 | 894 | PF00018 | 0.531 |
LIG_SH3_3 | 934 | 940 | PF00018 | 0.693 |
LIG_Sin3_3 | 467 | 474 | PF02671 | 0.365 |
LIG_SUMO_SIM_anti_2 | 694 | 700 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 344 | 350 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 677 | 688 | PF11976 | 0.658 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.448 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.558 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.482 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.448 |
LIG_WRC_WIRS_1 | 646 | 651 | PF05994 | 0.648 |
LIG_WRPW_2 | 59 | 62 | PF00400 | 0.400 |
LIG_WW_3 | 890 | 894 | PF00397 | 0.521 |
MOD_CDK_SPK_2 | 736 | 741 | PF00069 | 0.797 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 576 | 583 | PF00069 | 0.505 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.680 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.695 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.564 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.471 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.678 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.730 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.639 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.575 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.646 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.647 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.614 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.785 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.623 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.675 |
MOD_CK1_1 | 817 | 823 | PF00069 | 0.688 |
MOD_CK1_1 | 867 | 873 | PF00069 | 0.657 |
MOD_CK1_1 | 882 | 888 | PF00069 | 0.725 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.601 |
MOD_CK1_1 | 969 | 975 | PF00069 | 0.615 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.207 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.590 |
MOD_CK2_1 | 854 | 860 | PF00069 | 0.712 |
MOD_CK2_1 | 953 | 959 | PF00069 | 0.671 |
MOD_Cter_Amidation | 521 | 524 | PF01082 | 0.618 |
MOD_DYRK1A_RPxSP_1 | 533 | 537 | PF00069 | 0.524 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.572 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.555 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.665 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.625 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.487 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.402 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.583 |
MOD_GlcNHglycan | 270 | 275 | PF01048 | 0.471 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.738 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.674 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.504 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.605 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.649 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.537 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.551 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.613 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.713 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.761 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.678 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.622 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.668 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.708 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.672 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.506 |
MOD_GlcNHglycan | 940 | 943 | PF01048 | 0.710 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.579 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.597 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.798 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.662 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.543 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.312 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.351 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.651 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.706 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.784 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.588 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.800 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.684 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.658 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.559 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.635 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.552 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.628 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.665 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.776 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.670 |
MOD_GSK3_1 | 875 | 882 | PF00069 | 0.583 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.422 |
MOD_GSK3_1 | 962 | 969 | PF00069 | 0.632 |
MOD_GSK3_1 | 971 | 978 | PF00069 | 0.608 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.702 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.711 |
MOD_N-GLC_1 | 768 | 773 | PF02516 | 0.518 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.511 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.525 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.343 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.346 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.458 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.569 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.348 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.623 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.553 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.683 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.646 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.355 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.529 |
MOD_NEK2_1 | 944 | 949 | PF00069 | 0.671 |
MOD_NEK2_1 | 968 | 973 | PF00069 | 0.685 |
MOD_NEK2_2 | 716 | 721 | PF00069 | 0.667 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.388 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.653 |
MOD_PIKK_1 | 661 | 667 | PF00454 | 0.494 |
MOD_PK_1 | 478 | 484 | PF00069 | 0.357 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.563 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.572 |
MOD_PKA_1 | 674 | 680 | PF00069 | 0.601 |
MOD_PKA_1 | 721 | 727 | PF00069 | 0.656 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.585 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.709 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.622 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.513 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.591 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.585 |
MOD_PKA_2 | 721 | 727 | PF00069 | 0.642 |
MOD_PKA_2 | 794 | 800 | PF00069 | 0.572 |
MOD_PKA_2 | 944 | 950 | PF00069 | 0.728 |
MOD_PKA_2 | 969 | 975 | PF00069 | 0.583 |
MOD_PKB_1 | 834 | 842 | PF00069 | 0.694 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.347 |
MOD_Plk_1 | 797 | 803 | PF00069 | 0.656 |
MOD_Plk_2-3 | 645 | 651 | PF00069 | 0.528 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.509 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.388 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.497 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.567 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.335 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.576 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.593 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.594 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.602 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.362 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.379 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.462 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.607 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.628 |
MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.738 |
MOD_ProDKin_1 | 875 | 881 | PF00069 | 0.721 |
MOD_ProDKin_1 | 933 | 939 | PF00069 | 0.786 |
MOD_ProDKin_1 | 962 | 968 | PF00069 | 0.673 |
MOD_SUMO_rev_2 | 266 | 274 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 730 | 735 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 739 | 748 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 927 | 934 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_4 | 756 | 762 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 530 | 533 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 673 | 675 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 793 | 796 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 822 | 825 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 834 | 836 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 892 | 895 | PF00400 | 0.779 |
TRG_ER_diArg_1 | 900 | 903 | PF00400 | 0.665 |
TRG_NES_CRM1_1 | 694 | 708 | PF08389 | 0.642 |
TRG_NLS_MonoExtN_4 | 117 | 124 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 574 | 578 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4R5 | Leptomonas seymouri | 44% | 88% |
A0A3S5H6C9 | Leishmania donovani | 85% | 99% |
A4H5L8 | Leishmania braziliensis | 67% | 100% |
A4HTV6 | Leishmania infantum | 84% | 99% |
Q4QHY2 | Leishmania major | 83% | 99% |