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:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0005876 | spindle microtubule | 7 | 1 |
GO:0031616 | spindle pole centrosome | 4 | 1 |
GO:0032133 | chromosome passenger complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051233 | spindle midzone | 2 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AYM5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
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:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0032465 | regulation of cytokinesis | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051302 | regulation of cell division | 4 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0035173 | histone kinase activity | 4 | 1 |
GO:0035174 | obsolete histone serine kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.770 |
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.842 |
CLV_NRD_NRD_1 | 888 | 890 | PF00675 | 0.739 |
CLV_PCSK_FUR_1 | 311 | 315 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 1017 | 1019 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 710 | 712 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.842 |
CLV_PCSK_KEX2_1 | 888 | 890 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 1017 | 1019 | PF00082 | 0.818 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 1013 | 1019 | PF00082 | 0.655 |
CLV_PCSK_PC7_1 | 884 | 890 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 1028 | 1032 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.747 |
CLV_Separin_Metazoa | 149 | 153 | PF03568 | 0.561 |
DEG_SPOP_SBC_1 | 1003 | 1007 | PF00917 | 0.752 |
DEG_SPOP_SBC_1 | 808 | 812 | PF00917 | 0.727 |
DOC_CKS1_1 | 594 | 599 | PF01111 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 244 | PF00134 | 0.592 |
DOC_CYCLIN_yCln2_LP_2 | 258 | 264 | PF00134 | 0.565 |
DOC_MAPK_gen_1 | 311 | 321 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 313 | 321 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 607 | 615 | PF00069 | 0.591 |
DOC_PP1_RVXF_1 | 1026 | 1032 | PF00149 | 0.803 |
DOC_PP4_FxxP_1 | 180 | 183 | PF00568 | 0.707 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.715 |
DOC_PP4_FxxP_1 | 244 | 247 | PF00568 | 0.727 |
DOC_USP7_MATH_1 | 1003 | 1007 | PF00917 | 0.841 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 747 | 751 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 875 | 879 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 922 | 926 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.756 |
DOC_USP7_UBL2_3 | 1017 | 1021 | PF12436 | 0.752 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 785 | 790 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 811 | 816 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.860 |
LIG_14-3-3_CanoR_1 | 1018 | 1027 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 430 | 438 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 481 | 486 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 549 | 556 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 743 | 747 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 780 | 789 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 813 | 819 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 982 | 990 | PF00244 | 0.824 |
LIG_Actin_WH2_2 | 415 | 432 | PF00022 | 0.433 |
LIG_AP2alpha_2 | 240 | 242 | PF02296 | 0.544 |
LIG_APCC_ABBA_1 | 321 | 326 | PF00400 | 0.433 |
LIG_BIR_III_2 | 952 | 956 | PF00653 | 0.697 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.786 |
LIG_BRCT_BRCA1_1 | 619 | 623 | PF00533 | 0.791 |
LIG_BRCT_BRCA1_1 | 761 | 765 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 840 | 844 | PF00533 | 0.812 |
LIG_BRCT_BRCA1_1 | 927 | 931 | PF00533 | 0.574 |
LIG_Clathr_ClatBox_1 | 541 | 545 | PF01394 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 488 | 497 | PF00928 | 0.526 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.526 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.638 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.823 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.586 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.831 |
LIG_FHA_1 | 978 | 984 | PF00498 | 0.725 |
LIG_FHA_1 | 985 | 991 | PF00498 | 0.651 |
LIG_FHA_2 | 1031 | 1037 | PF00498 | 0.735 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.763 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.712 |
LIG_FHA_2 | 798 | 804 | PF00498 | 0.690 |
LIG_FHA_2 | 892 | 898 | PF00498 | 0.728 |
LIG_Integrin_RGD_1 | 895 | 897 | PF01839 | 0.733 |
LIG_LIR_Apic_2 | 178 | 183 | PF02991 | 0.682 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.735 |
LIG_LIR_Apic_2 | 469 | 475 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 38 | 47 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 740 | 747 | PF02991 | 0.745 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 740 | 744 | PF02991 | 0.801 |
LIG_LIR_Nem_3 | 762 | 768 | PF02991 | 0.728 |
LIG_MLH1_MIPbox_1 | 108 | 112 | PF16413 | 0.786 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.786 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.694 |
LIG_PTB_Apo_2 | 322 | 329 | PF02174 | 0.433 |
LIG_PTB_Phospho_1 | 322 | 328 | PF10480 | 0.433 |
LIG_REV1ctd_RIR_1 | 109 | 117 | PF16727 | 0.793 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.635 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.433 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.526 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.730 |
LIG_SH2_STAT3 | 856 | 859 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.721 |
LIG_SH3_1 | 994 | 1000 | PF00018 | 0.681 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.558 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.698 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.621 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.246 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.574 |
LIG_SH3_3 | 994 | 1000 | PF00018 | 0.775 |
LIG_Sin3_3 | 89 | 96 | PF02671 | 0.732 |
LIG_SUMO_SIM_anti_2 | 31 | 38 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 96 | 101 | PF11976 | 0.659 |
LIG_SUMO_SIM_par_1 | 984 | 992 | PF11976 | 0.722 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.730 |
LIG_WRC_WIRS_1 | 696 | 701 | PF05994 | 0.552 |
LIG_WRC_WIRS_1 | 738 | 743 | PF05994 | 0.819 |
LIG_WW_3 | 953 | 957 | PF00397 | 0.689 |
MOD_CDK_SPxK_1 | 270 | 276 | PF00069 | 0.819 |
MOD_CDK_SPxxK_3 | 270 | 277 | PF00069 | 0.820 |
MOD_CDK_SPxxK_3 | 663 | 670 | PF00069 | 0.715 |
MOD_CK1_1 | 1020 | 1026 | PF00069 | 0.562 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.818 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.580 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.586 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.706 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.475 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.435 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.412 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.829 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.781 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.814 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.665 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.657 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.661 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.601 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.835 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.658 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.621 |
MOD_CK1_1 | 838 | 844 | PF00069 | 0.661 |
MOD_CK1_1 | 846 | 852 | PF00069 | 0.638 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.682 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.680 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.729 |
MOD_CK1_1 | 925 | 931 | PF00069 | 0.745 |
MOD_CK1_1 | 932 | 938 | PF00069 | 0.679 |
MOD_CK1_1 | 945 | 951 | PF00069 | 0.649 |
MOD_CK1_1 | 986 | 992 | PF00069 | 0.734 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.771 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.732 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.714 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.246 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.575 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.386 |
MOD_Cter_Amidation | 295 | 298 | PF01082 | 0.526 |
MOD_Cter_Amidation | 777 | 780 | PF01082 | 0.764 |
MOD_DYRK1A_RPxSP_1 | 277 | 281 | PF00069 | 0.718 |
MOD_GlcNHglycan | 1013 | 1016 | PF01048 | 0.559 |
MOD_GlcNHglycan | 1022 | 1025 | PF01048 | 0.523 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.727 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.729 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.422 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.530 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.429 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.727 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.433 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.526 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.438 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.740 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.562 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.652 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.674 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.645 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.823 |
MOD_GlcNHglycan | 803 | 807 | PF01048 | 0.751 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.640 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.648 |
MOD_GlcNHglycan | 877 | 880 | PF01048 | 0.700 |
MOD_GlcNHglycan | 968 | 971 | PF01048 | 0.682 |
MOD_GSK3_1 | 1019 | 1026 | PF00069 | 0.632 |
MOD_GSK3_1 | 1032 | 1039 | PF00069 | 0.626 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.604 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.650 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.530 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.328 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.810 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.696 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.700 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.663 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.652 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.739 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.601 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.701 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.501 |
MOD_GSK3_1 | 875 | 882 | PF00069 | 0.617 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.651 |
MOD_GSK3_1 | 912 | 919 | PF00069 | 0.829 |
MOD_GSK3_1 | 925 | 932 | PF00069 | 0.611 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.678 |
MOD_GSK3_1 | 941 | 948 | PF00069 | 0.573 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.553 |
MOD_GSK3_1 | 977 | 984 | PF00069 | 0.618 |
MOD_N-GLC_1 | 790 | 795 | PF02516 | 0.859 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.683 |
MOD_N-GLC_2 | 451 | 453 | PF02516 | 0.246 |
MOD_NEK2_1 | 1019 | 1024 | PF00069 | 0.522 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.783 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.698 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.764 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.692 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.526 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.314 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.199 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.691 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.814 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.649 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.807 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.813 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.650 |
MOD_NEK2_1 | 929 | 934 | PF00069 | 0.779 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.704 |
MOD_NEK2_1 | 965 | 970 | PF00069 | 0.608 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.646 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.246 |
MOD_NEK2_2 | 434 | 439 | PF00069 | 0.246 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.784 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.722 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.711 |
MOD_PIKK_1 | 854 | 860 | PF00454 | 0.763 |
MOD_PKA_1 | 1017 | 1023 | PF00069 | 0.671 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.638 |
MOD_PKA_1 | 779 | 785 | PF00069 | 0.849 |
MOD_PKA_1 | 888 | 894 | PF00069 | 0.735 |
MOD_PKA_2 | 1017 | 1023 | PF00069 | 0.671 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.690 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.763 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.784 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.732 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.409 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.433 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.475 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.718 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.642 |
MOD_PKA_2 | 742 | 748 | PF00069 | 0.521 |
MOD_PKA_2 | 779 | 785 | PF00069 | 0.716 |
MOD_PKA_2 | 888 | 894 | PF00069 | 0.735 |
MOD_PKA_2 | 907 | 913 | PF00069 | 0.678 |
MOD_PKA_2 | 981 | 987 | PF00069 | 0.633 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.714 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.575 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.724 |
MOD_Plk_1 | 773 | 779 | PF00069 | 0.573 |
MOD_Plk_1 | 896 | 902 | PF00069 | 0.823 |
MOD_Plk_1 | 922 | 928 | PF00069 | 0.817 |
MOD_Plk_2-3 | 1032 | 1038 | PF00069 | 0.790 |
MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.816 |
MOD_Plk_2-3 | 916 | 922 | PF00069 | 0.681 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.706 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.586 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.512 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.243 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.526 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.535 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.721 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.825 |
MOD_Plk_4 | 835 | 841 | PF00069 | 0.756 |
MOD_Plk_4 | 961 | 967 | PF00069 | 0.555 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.613 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.549 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.757 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.625 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.806 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.475 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.655 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.526 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.433 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.570 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.726 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.488 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.714 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.639 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.751 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.735 |
MOD_ProDKin_1 | 785 | 791 | PF00069 | 0.821 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.746 |
MOD_ProDKin_1 | 811 | 817 | PF00069 | 0.529 |
MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.860 |
MOD_SUMO_rev_2 | 227 | 235 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 507 | 517 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_1 | 513 | 518 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 261 | 266 | PF01217 | 0.651 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.730 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.246 |
TRG_ER_diArg_1 | 779 | 781 | PF00400 | 0.842 |
TRG_ER_diArg_1 | 888 | 890 | PF00400 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X078 | Leishmania donovani | 82% | 100% |
A4HF89 | Leishmania braziliensis | 61% | 100% |
A4I2H1 | Leishmania infantum | 82% | 100% |
Q4Q8U7 | Leishmania major | 81% | 100% |