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:0000407 | phagophore assembly site | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005768 | endosome | 7 | 1 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0005942 | phosphatidylinositol 3-kinase complex | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034271 | phosphatidylinositol 3-kinase complex, class III, type I | 5 | 1 |
GO:0034272 | phosphatidylinositol 3-kinase complex, class III, type II | 5 | 1 |
GO:0035032 | phosphatidylinositol 3-kinase complex, class III | 4 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AX47
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 7 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0000045 | autophagosome assembly | 6 | 1 |
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 2 |
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0006914 | autophagy | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007033 | vacuole organization | 5 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0008654 | phospholipid biosynthetic process | 5 | 2 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030242 | autophagy of peroxisome | 4 | 1 |
GO:0036092 | phosphatidylinositol-3-phosphate biosynthetic process | 8 | 1 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 2 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 2 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 2 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1905037 | autophagosome organization | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016303 | 1-phosphatidylinositol-3-kinase activity | 6 | 6 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0035004 | phosphatidylinositol 3-kinase activity | 5 | 6 |
GO:0052742 | phosphatidylinositol kinase activity | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 650 | 654 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 666 | 670 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 1007 | 1009 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 516 | 518 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 900 | 904 | PF00082 | 0.335 |
CLV_Separin_Metazoa | 914 | 918 | PF03568 | 0.335 |
DEG_APCC_DBOX_1 | 1037 | 1045 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.478 |
DEG_APCC_DBOX_1 | 44 | 52 | PF00400 | 0.522 |
DEG_APCC_DBOX_1 | 899 | 907 | PF00400 | 0.335 |
DEG_MDM2_SWIB_1 | 1073 | 1080 | PF02201 | 0.504 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.434 |
DOC_ANK_TNKS_1 | 458 | 465 | PF00023 | 0.389 |
DOC_CDC14_PxL_1 | 217 | 225 | PF14671 | 0.658 |
DOC_CKS1_1 | 610 | 615 | PF01111 | 0.501 |
DOC_CKS1_1 | 783 | 788 | PF01111 | 0.757 |
DOC_CKS1_1 | 870 | 875 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 563 | 573 | PF00134 | 0.544 |
DOC_CYCLIN_yClb1_LxF_4 | 750 | 755 | PF00134 | 0.370 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 744 | 753 | PF00134 | 0.309 |
DOC_CYCLIN_yCln2_LP_2 | 137 | 143 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 1008 | 1015 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 354 | 360 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 396 | 404 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 45 | 53 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 707 | 716 | PF00069 | 0.716 |
DOC_MAPK_gen_1 | 976 | 984 | PF00069 | 0.335 |
DOC_MAPK_HePTP_8 | 593 | 605 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 1008 | 1017 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 1043 | 1052 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 596 | 605 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 846 | 854 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 864 | 871 | PF00069 | 0.398 |
DOC_MAPK_NFAT4_5 | 864 | 872 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 383 | 389 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 600 | 606 | PF00149 | 0.353 |
DOC_PP1_RVXF_1 | 675 | 682 | PF00149 | 0.675 |
DOC_PP1_RVXF_1 | 750 | 756 | PF00149 | 0.375 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.543 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.602 |
DOC_PP4_FxxP_1 | 681 | 684 | PF00568 | 0.545 |
DOC_PP4_FxxP_1 | 824 | 827 | PF00568 | 0.500 |
DOC_PP4_FxxP_1 | 971 | 974 | PF00568 | 0.335 |
DOC_PP4_MxPP_1 | 216 | 219 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.744 |
DOC_USP7_UBL2_3 | 1043 | 1047 | PF12436 | 0.433 |
DOC_USP7_UBL2_3 | 592 | 596 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 775 | 780 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 1008 | 1014 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 547 | 555 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 583 | 593 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 602 | 610 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 707 | 717 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 719 | 729 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 752 | 760 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 907 | 916 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 922 | 928 | PF00244 | 0.294 |
LIG_Actin_WH2_2 | 39 | 56 | PF00022 | 0.487 |
LIG_Actin_WH2_2 | 746 | 761 | PF00022 | 0.439 |
LIG_BIR_III_2 | 831 | 835 | PF00653 | 0.330 |
LIG_BIR_III_4 | 653 | 657 | PF00653 | 0.781 |
LIG_BRCT_BRCA1_1 | 440 | 444 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 694 | 698 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 989 | 993 | PF00533 | 0.335 |
LIG_Clathr_ClatBox_1 | 507 | 511 | PF01394 | 0.453 |
LIG_Clathr_ClatBox_1 | 86 | 90 | PF01394 | 0.594 |
LIG_Clathr_ClatBox_1 | 955 | 959 | PF01394 | 0.335 |
LIG_CSK_EPIYA_1 | 772 | 776 | PF00017 | 0.582 |
LIG_deltaCOP1_diTrp_1 | 134 | 139 | PF00928 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 20 | 31 | PF00928 | 0.705 |
LIG_EH1_1 | 565 | 573 | PF00400 | 0.537 |
LIG_FHA_1 | 1056 | 1062 | PF00498 | 0.408 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.655 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.457 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.527 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.598 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.352 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.646 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.409 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.510 |
LIG_FHA_1 | 732 | 738 | PF00498 | 0.494 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.387 |
LIG_FHA_1 | 910 | 916 | PF00498 | 0.510 |
LIG_FHA_1 | 932 | 938 | PF00498 | 0.335 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.654 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.433 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.529 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.536 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.364 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.520 |
LIG_GSK3_LRP6_1 | 682 | 688 | PF00069 | 0.549 |
LIG_Integrin_RGD_1 | 292 | 294 | PF01839 | 0.558 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.573 |
LIG_LIR_Apic_2 | 397 | 403 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 607 | 613 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 1002 | 1011 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 1071 | 1080 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 134 | 143 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 309 | 319 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 754 | 763 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 990 | 999 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 1002 | 1007 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 1071 | 1076 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 754 | 758 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 872 | 877 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 893 | 898 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 924 | 930 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 959 | 963 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 990 | 996 | PF02991 | 0.335 |
LIG_MLH1_MIPbox_1 | 440 | 444 | PF16413 | 0.335 |
LIG_NRBOX | 1014 | 1020 | PF00104 | 0.335 |
LIG_NRBOX | 348 | 354 | PF00104 | 0.478 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.482 |
LIG_PCNA_PIPBox_1 | 899 | 908 | PF02747 | 0.335 |
LIG_PCNA_yPIPBox_3 | 558 | 569 | PF02747 | 0.543 |
LIG_PCNA_yPIPBox_3 | 899 | 907 | PF02747 | 0.335 |
LIG_PCNA_yPIPBox_3 | 976 | 985 | PF02747 | 0.335 |
LIG_Pex14_2 | 1073 | 1077 | PF04695 | 0.496 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.443 |
LIG_REV1ctd_RIR_1 | 311 | 319 | PF16727 | 0.572 |
LIG_SH2_CRK | 1004 | 1008 | PF00017 | 0.335 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.682 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.306 |
LIG_SH2_CRK | 610 | 614 | PF00017 | 0.521 |
LIG_SH2_CRK | 874 | 878 | PF00017 | 0.401 |
LIG_SH2_CRK | 930 | 934 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 103 | 107 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 171 | 175 | PF00017 | 0.604 |
LIG_SH2_NCK_1 | 27 | 31 | PF00017 | 0.642 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 479 | 483 | PF00017 | 0.453 |
LIG_SH2_SRC | 265 | 268 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 103 | 107 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 923 | 927 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 1060 | 1063 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 905 | 908 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 923 | 926 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 930 | 933 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 962 | 965 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 999 | 1002 | PF00017 | 0.335 |
LIG_SH3_1 | 680 | 686 | PF00018 | 0.640 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.668 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.528 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.604 |
LIG_SH3_3 | 680 | 686 | PF00018 | 0.622 |
LIG_SH3_3 | 690 | 696 | PF00018 | 0.654 |
LIG_SH3_3 | 726 | 732 | PF00018 | 0.454 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.592 |
LIG_SH3_3 | 780 | 786 | PF00018 | 0.653 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.388 |
LIG_SH3_3 | 967 | 973 | PF00018 | 0.335 |
LIG_SUMO_SIM_anti_2 | 2 | 11 | PF11976 | 0.627 |
LIG_SUMO_SIM_anti_2 | 711 | 718 | PF11976 | 0.528 |
LIG_SUMO_SIM_anti_2 | 980 | 986 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 139 | 145 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.345 |
LIG_TRAF2_1 | 816 | 819 | PF00917 | 0.667 |
LIG_TYR_ITIM | 903 | 908 | PF00017 | 0.335 |
LIG_TYR_ITSM | 870 | 877 | PF00017 | 0.505 |
LIG_Vh1_VBS_1 | 1065 | 1083 | PF01044 | 0.468 |
LIG_WRC_WIRS_1 | 129 | 134 | PF05994 | 0.558 |
LIG_WRC_WIRS_1 | 892 | 897 | PF05994 | 0.519 |
LIG_WRC_WIRS_1 | 932 | 937 | PF05994 | 0.335 |
MOD_CDK_SPxK_1 | 609 | 615 | PF00069 | 0.498 |
MOD_CDK_SPxK_1 | 869 | 875 | PF00069 | 0.386 |
MOD_CDK_SPxxK_3 | 609 | 616 | PF00069 | 0.501 |
MOD_CK1_1 | 1068 | 1074 | PF00069 | 0.433 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.563 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.684 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.771 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.526 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.516 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.773 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.781 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.753 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.543 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.681 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.383 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.408 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.673 |
MOD_CK2_1 | 908 | 914 | PF00069 | 0.374 |
MOD_GlcNHglycan | 1001 | 1004 | PF01048 | 0.335 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.466 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.675 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.563 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.453 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.729 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.751 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.565 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.674 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.588 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.757 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.713 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.600 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.476 |
MOD_GlcNHglycan | 797 | 800 | PF01048 | 0.835 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.567 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.538 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.454 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.545 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.455 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.469 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.453 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.479 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.418 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.721 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.472 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.658 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.756 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.624 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.648 |
MOD_GSK3_1 | 890 | 897 | PF00069 | 0.411 |
MOD_GSK3_1 | 987 | 994 | PF00069 | 0.453 |
MOD_GSK3_1 | 999 | 1006 | PF00069 | 0.291 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.525 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.770 |
MOD_N-GLC_1 | 804 | 809 | PF02516 | 0.713 |
MOD_N-GLC_1 | 909 | 914 | PF02516 | 0.517 |
MOD_N-GLC_2 | 318 | 320 | PF02516 | 0.667 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.586 |
MOD_NEK2_1 | 1050 | 1055 | PF00069 | 0.443 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.509 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.542 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.487 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.688 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.335 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.344 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.545 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.487 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.383 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.513 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.495 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.483 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.596 |
MOD_NEK2_2 | 1003 | 1008 | PF00069 | 0.453 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.413 |
MOD_NEK2_2 | 438 | 443 | PF00069 | 0.335 |
MOD_NEK2_2 | 532 | 537 | PF00069 | 0.460 |
MOD_PIKK_1 | 1055 | 1061 | PF00454 | 0.411 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.619 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.415 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.544 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.411 |
MOD_PIKK_1 | 685 | 691 | PF00454 | 0.650 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.763 |
MOD_PIKK_1 | 947 | 953 | PF00454 | 0.335 |
MOD_PK_1 | 64 | 70 | PF00069 | 0.472 |
MOD_PKA_1 | 516 | 522 | PF00069 | 0.479 |
MOD_PKA_1 | 542 | 548 | PF00069 | 0.472 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.494 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.698 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.415 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.596 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.488 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.414 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.574 |
MOD_PKA_2 | 751 | 757 | PF00069 | 0.381 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.380 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.403 |
MOD_PKB_1 | 707 | 715 | PF00069 | 0.642 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.518 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.335 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.721 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.435 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.613 |
MOD_Plk_4 | 1009 | 1015 | PF00069 | 0.248 |
MOD_Plk_4 | 1068 | 1074 | PF00069 | 0.433 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.411 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.639 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.478 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.597 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.660 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.335 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.331 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.552 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.441 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.765 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.454 |
MOD_Plk_4 | 891 | 897 | PF00069 | 0.406 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.506 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.596 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.498 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.728 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.746 |
MOD_ProDKin_1 | 775 | 781 | PF00069 | 0.762 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.736 |
MOD_ProDKin_1 | 869 | 875 | PF00069 | 0.386 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.473 |
MOD_SUMO_rev_2 | 316 | 325 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 990 | 998 | PF00179 | 0.335 |
TRG_DiLeu_BaEn_1 | 382 | 387 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_2 | 484 | 490 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 382 | 388 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 536 | 541 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 951 | 956 | PF01217 | 0.335 |
TRG_DiLeu_LyEn_5 | 382 | 387 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 1004 | 1007 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 874 | 877 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 905 | 908 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 930 | 933 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 676 | 678 | PF00400 | 0.653 |
TRG_NES_CRM1_1 | 499 | 511 | PF08389 | 0.335 |
TRG_NES_CRM1_1 | 887 | 901 | PF08389 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 456 | 461 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 542 | 546 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 574 | 578 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 954 | 959 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P435 | Leptomonas seymouri | 59% | 96% |
A0A3Q8IGA3 | Leishmania donovani | 95% | 100% |
A4HDR3 | Leishmania braziliensis | 86% | 100% |
A4I109 | Leishmania infantum | 94% | 100% |
Q4QAC9 | Leishmania major | 93% | 100% |