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:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AEN1
Term | Name | Level | Count |
---|---|---|---|
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:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0008654 | phospholipid biosynthetic process | 5 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 2 |
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:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016307 | phosphatidylinositol phosphate kinase activity | 5 | 7 |
GO:0016308 | 1-phosphatidylinositol-4-phosphate 5-kinase activity | 6 | 2 |
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 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 614 | 618 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 702 | 706 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 977 | 981 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 1048 | 1050 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.832 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.760 |
CLV_NRD_NRD_1 | 773 | 775 | PF00675 | 0.335 |
CLV_PCSK_FUR_1 | 317 | 321 | PF00082 | 0.697 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.642 |
CLV_PCSK_FUR_1 | 49 | 53 | PF00082 | 0.517 |
CLV_PCSK_FUR_1 | 690 | 694 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 1048 | 1050 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.749 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.657 |
CLV_PCSK_PC7_1 | 249 | 255 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 838 | 842 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 849 | 853 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 915 | 919 | PF00082 | 0.453 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.562 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.532 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.702 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 622 | 626 | PF00917 | 0.576 |
DOC_ANK_TNKS_1 | 530 | 537 | PF00023 | 0.681 |
DOC_CKS1_1 | 1006 | 1011 | PF01111 | 0.358 |
DOC_CKS1_1 | 819 | 824 | PF01111 | 0.335 |
DOC_CYCLIN_RxL_1 | 127 | 139 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 858 | 868 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 1062 | 1072 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 249 | 257 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 48 | 59 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 762 | 771 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 52 | 61 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 663 | 671 | PF00069 | 0.492 |
DOC_PP2B_LxvP_1 | 1002 | 1005 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 819 | 822 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 746 | 750 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 981 | 985 | PF00917 | 0.358 |
DOC_USP7_UBL2_3 | 616 | 620 | PF12436 | 0.750 |
DOC_WW_Pin1_4 | 1005 | 1010 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 742 | 747 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 972 | 977 | PF00397 | 0.248 |
LIG_14-3-3_CanoR_1 | 1048 | 1054 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 124 | 134 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 155 | 164 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 590 | 596 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 690 | 696 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 741 | 745 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 786 | 792 | PF00244 | 0.335 |
LIG_14-3-3_CterR_2 | 1069 | 1072 | PF00244 | 0.389 |
LIG_AP2alpha_2 | 581 | 583 | PF02296 | 0.453 |
LIG_BIR_III_4 | 266 | 270 | PF00653 | 0.764 |
LIG_BIR_III_4 | 705 | 709 | PF00653 | 0.681 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 903 | 907 | PF00533 | 0.335 |
LIG_CtBP_PxDLS_1 | 459 | 463 | PF00389 | 0.696 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.615 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.554 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.644 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.338 |
LIG_FHA_1 | 914 | 920 | PF00498 | 0.335 |
LIG_FHA_2 | 1006 | 1012 | PF00498 | 0.366 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.561 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.659 |
LIG_FHA_2 | 944 | 950 | PF00498 | 0.511 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.550 |
LIG_LIR_Apic_2 | 399 | 404 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 1030 | 1037 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 581 | 591 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 682 | 691 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 895 | 902 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 988 | 998 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 1018 | 1024 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 1030 | 1034 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 1061 | 1067 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 581 | 586 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 850 | 855 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 988 | 994 | PF02991 | 0.335 |
LIG_LRP6_Inhibitor_1 | 675 | 681 | PF00058 | 0.416 |
LIG_MYND_1 | 972 | 976 | PF01753 | 0.389 |
LIG_MYND_2 | 863 | 867 | PF01753 | 0.335 |
LIG_PDZ_Class_2 | 1067 | 1072 | PF00595 | 0.335 |
LIG_Pex14_2 | 1040 | 1044 | PF04695 | 0.325 |
LIG_Pex14_2 | 691 | 695 | PF04695 | 0.470 |
LIG_SH2_CRK | 1031 | 1035 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 265 | 269 | PF00017 | 0.759 |
LIG_SH2_NCK_1 | 796 | 800 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 991 | 994 | PF00017 | 0.335 |
LIG_SH2_SRC | 401 | 404 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 1059 | 1063 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 986 | 990 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 1007 | 1010 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 1021 | 1024 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 755 | 758 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 824 | 827 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 991 | 994 | PF00017 | 0.335 |
LIG_SH3_3 | 1050 | 1056 | PF00018 | 0.335 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.773 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.626 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.720 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.690 |
LIG_SH3_3 | 840 | 846 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 916 | 921 | PF11976 | 0.453 |
LIG_SxIP_EBH_1 | 690 | 702 | PF03271 | 0.466 |
LIG_TRAF2_1 | 1015 | 1018 | PF00917 | 0.453 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.672 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.556 |
LIG_TRAF2_1 | 512 | 515 | PF00917 | 0.738 |
LIG_TRAF2_1 | 908 | 911 | PF00917 | 0.313 |
LIG_TRFH_1 | 428 | 432 | PF08558 | 0.555 |
LIG_TYR_ITIM | 1019 | 1024 | PF00017 | 0.335 |
LIG_UBA3_1 | 117 | 122 | PF00899 | 0.521 |
LIG_UBA3_1 | 56 | 63 | PF00899 | 0.646 |
LIG_WRC_WIRS_1 | 1037 | 1042 | PF05994 | 0.335 |
LIG_WW_3 | 846 | 850 | PF00397 | 0.335 |
MOD_CDC14_SPxK_1 | 397 | 400 | PF00782 | 0.666 |
MOD_CDC14_SPxK_1 | 745 | 748 | PF00782 | 0.335 |
MOD_CDK_SPxK_1 | 394 | 400 | PF00069 | 0.695 |
MOD_CDK_SPxK_1 | 742 | 748 | PF00069 | 0.335 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.706 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 302 | 309 | PF00069 | 0.572 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.735 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.619 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.704 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.664 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.672 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.679 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.767 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.589 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.679 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.575 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.695 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.605 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.696 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.335 |
MOD_CK1_1 | 975 | 981 | PF00069 | 0.322 |
MOD_CK2_1 | 1011 | 1017 | PF00069 | 0.335 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.742 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.557 |
MOD_CK2_1 | 880 | 886 | PF00069 | 0.262 |
MOD_CK2_1 | 905 | 911 | PF00069 | 0.335 |
MOD_CK2_1 | 943 | 949 | PF00069 | 0.453 |
MOD_Cter_Amidation | 317 | 320 | PF01082 | 0.651 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.647 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.763 |
MOD_GlcNHglycan | 224 | 228 | PF01048 | 0.663 |
MOD_GlcNHglycan | 235 | 240 | PF01048 | 0.520 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.668 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.685 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.681 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.727 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.696 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.712 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.588 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.632 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.818 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.471 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.776 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.556 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.676 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.601 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.335 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.588 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.609 |
MOD_GlcNHglycan | 934 | 937 | PF01048 | 0.308 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.629 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.414 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.654 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.774 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.563 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.665 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.801 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.709 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.642 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.647 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.753 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.674 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.608 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.552 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.335 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.573 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.335 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.335 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.343 |
MOD_GSK3_1 | 970 | 977 | PF00069 | 0.342 |
MOD_LATS_1 | 22 | 28 | PF00433 | 0.591 |
MOD_LATS_1 | 407 | 413 | PF00433 | 0.767 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.718 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.675 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.554 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.719 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.621 |
MOD_N-GLC_1 | 836 | 841 | PF02516 | 0.335 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.756 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.572 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.656 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.662 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.743 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.647 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.665 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.456 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.676 |
MOD_NEK2_1 | 868 | 873 | PF00069 | 0.326 |
MOD_NEK2_1 | 932 | 937 | PF00069 | 0.358 |
MOD_NEK2_2 | 797 | 802 | PF00069 | 0.335 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.693 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.614 |
MOD_PIKK_1 | 699 | 705 | PF00454 | 0.696 |
MOD_PIKK_1 | 936 | 942 | PF00454 | 0.453 |
MOD_PK_1 | 1049 | 1055 | PF00069 | 0.453 |
MOD_PKA_1 | 505 | 511 | PF00069 | 0.672 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.497 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.693 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.673 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.595 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.720 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.502 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.563 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.466 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.435 |
MOD_PKB_1 | 903 | 911 | PF00069 | 0.335 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.719 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.696 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.541 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.570 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.745 |
MOD_Plk_1 | 735 | 741 | PF00069 | 0.335 |
MOD_Plk_1 | 836 | 842 | PF00069 | 0.335 |
MOD_Plk_1 | 894 | 900 | PF00069 | 0.335 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.584 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.475 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.541 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.674 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.570 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.335 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.335 |
MOD_Plk_4 | 913 | 919 | PF00069 | 0.335 |
MOD_ProDKin_1 | 1005 | 1011 | PF00069 | 0.358 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.698 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.804 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.702 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.619 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.493 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.602 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.663 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.678 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.643 |
MOD_ProDKin_1 | 742 | 748 | PF00069 | 0.335 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.335 |
MOD_ProDKin_1 | 972 | 978 | PF00069 | 0.248 |
TRG_AP2beta_CARGO_1 | 581 | 590 | PF09066 | 0.456 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.691 |
TRG_DiLeu_BaEn_1 | 768 | 773 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 1017 | 1023 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 490 | 496 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 1021 | 1024 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 1031 | 1034 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 1064 | 1067 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 991 | 994 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.805 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 691 | 693 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 714 | 716 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 725 | 728 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 902 | 905 | PF00400 | 0.335 |
TRG_NES_CRM1_1 | 679 | 689 | PF08389 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 132 | 137 | PF00026 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T7 | Leptomonas seymouri | 51% | 99% |
A0A3Q8ILT5 | Leishmania donovani | 90% | 99% |
A4HM89 | Leishmania braziliensis | 69% | 98% |
A4IAV3 | Leishmania infantum | 90% | 95% |
E9B5T7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |