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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H5L8
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 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:0007096 | regulation of exit from mitosis | 7 | 6 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0010564 | regulation of cell cycle process | 5 | 6 |
GO:0016311 | dephosphorylation | 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:0050789 | regulation of biological process | 2 | 6 |
GO:0050794 | regulation of cellular process | 3 | 6 |
GO:0051726 | regulation of cell cycle | 4 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 6 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 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: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 | 6 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 6 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 5 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016791 | phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 914 | 916 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 949 | 951 | PF00675 | 0.567 |
CLV_PCSK_FUR_1 | 940 | 944 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 752 | 754 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 914 | 916 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 942 | 944 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 949 | 951 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 598 | 600 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 694 | 696 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 799 | 801 | PF00082 | 0.739 |
CLV_PCSK_PC1ET2_1 | 942 | 944 | PF00082 | 0.703 |
CLV_PCSK_PC7_1 | 192 | 198 | PF00082 | 0.565 |
CLV_PCSK_PC7_1 | 938 | 944 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 1074 | 1078 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 914 | 918 | PF00082 | 0.600 |
CLV_Separin_Metazoa | 152 | 156 | PF03568 | 0.461 |
DEG_APCC_KENBOX_2 | 82 | 86 | PF00400 | 0.479 |
DEG_SCF_FBW7_1 | 6 | 13 | PF00400 | 0.559 |
DEG_SIAH_1 | 1058 | 1066 | PF03145 | 0.550 |
DEG_SPOP_SBC_1 | 1005 | 1009 | PF00917 | 0.569 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.673 |
DEG_SPOP_SBC_1 | 849 | 853 | PF00917 | 0.666 |
DEG_SPOP_SBC_1 | 98 | 102 | PF00917 | 0.585 |
DOC_CDC14_PxL_1 | 36 | 44 | PF14671 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 621 | 627 | PF00134 | 0.525 |
DOC_MAPK_DCC_7 | 570 | 580 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 351 | 360 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 570 | 580 | PF00069 | 0.572 |
DOC_MAPK_HePTP_8 | 348 | 360 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 1017 | 1025 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 571 | 580 | PF00069 | 0.450 |
DOC_PP2B_LxvP_1 | 1026 | 1029 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 572 | 575 | PF13499 | 0.568 |
DOC_PP2B_PxIxI_1 | 575 | 581 | PF00149 | 0.449 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.477 |
DOC_USP7_MATH_1 | 1005 | 1009 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 1065 | 1069 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 869 | 873 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 931 | 935 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 1050 | 1055 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 784 | 789 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 813 | 818 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 977 | 982 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 1034 | 1038 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 1052 | 1062 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 238 | 245 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 605 | 615 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 650 | 654 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 660 | 665 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 707 | 716 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 791 | 797 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 925 | 933 | PF00244 | 0.702 |
LIG_Actin_WH2_2 | 361 | 378 | PF00022 | 0.465 |
LIG_BIR_III_2 | 679 | 683 | PF00653 | 0.709 |
LIG_BRCT_BRCA1_1 | 825 | 829 | PF00533 | 0.672 |
LIG_CSL_BTD_1 | 843 | 846 | PF09270 | 0.539 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.422 |
LIG_CtBP_PxDLS_1 | 5 | 9 | PF00389 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 322 | 331 | PF00928 | 0.454 |
LIG_EH_1 | 84 | 88 | PF12763 | 0.415 |
LIG_eIF4E_1 | 369 | 375 | PF01652 | 0.463 |
LIG_eIF4E_1 | 912 | 918 | PF01652 | 0.525 |
LIG_EVH1_1 | 842 | 846 | PF00568 | 0.540 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.546 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.546 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.504 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.655 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.550 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.619 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.701 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.632 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.669 |
LIG_FHA_1 | 868 | 874 | PF00498 | 0.567 |
LIG_FHA_1 | 900 | 906 | PF00498 | 0.564 |
LIG_FHA_1 | 928 | 934 | PF00498 | 0.613 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.490 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.434 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.460 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.519 |
LIG_GBD_Chelix_1 | 360 | 368 | PF00786 | 0.449 |
LIG_GBD_Chelix_1 | 580 | 588 | PF00786 | 0.443 |
LIG_LIR_Apic_2 | 309 | 313 | PF02991 | 0.485 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 114 | 125 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 322 | 331 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 718 | 724 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 826 | 835 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 1016 | 1021 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 718 | 722 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 723 | 728 | PF02991 | 0.633 |
LIG_LYPXL_S_1 | 268 | 272 | PF13949 | 0.346 |
LIG_MLH1_MIPbox_1 | 825 | 829 | PF16413 | 0.672 |
LIG_MYND_1 | 480 | 484 | PF01753 | 0.563 |
LIG_NRBOX | 149 | 155 | PF00104 | 0.439 |
LIG_NRBOX | 25 | 31 | PF00104 | 0.404 |
LIG_PCNA_PIPBox_1 | 74 | 83 | PF02747 | 0.493 |
LIG_Pex14_1 | 261 | 265 | PF04695 | 0.546 |
LIG_Pex14_1 | 944 | 948 | PF04695 | 0.539 |
LIG_PTAP_UEV_1 | 1058 | 1063 | PF05743 | 0.553 |
LIG_SH2_CRK | 1018 | 1022 | PF00017 | 0.552 |
LIG_SH2_GRB2like | 495 | 498 | PF00017 | 0.540 |
LIG_SH2_SRC | 315 | 318 | PF00017 | 0.350 |
LIG_SH2_SRC | 386 | 389 | PF00017 | 0.501 |
LIG_SH2_SRC | 495 | 498 | PF00017 | 0.540 |
LIG_SH2_SRC | 564 | 567 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 824 | 828 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 927 | 931 | PF00017 | 0.757 |
LIG_SH2_STAP1 | 974 | 978 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 828 | 831 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 927 | 930 | PF00017 | 0.822 |
LIG_SH3_1 | 840 | 846 | PF00018 | 0.539 |
LIG_SH3_3 | 1048 | 1054 | PF00018 | 0.699 |
LIG_SH3_3 | 1056 | 1062 | PF00018 | 0.623 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.313 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.477 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.692 |
LIG_SH3_3 | 840 | 846 | PF00018 | 0.539 |
LIG_SH3_3 | 888 | 894 | PF00018 | 0.539 |
LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 758 | 766 | PF11976 | 0.689 |
LIG_SxIP_EBH_1 | 929 | 943 | PF03271 | 0.531 |
LIG_TRAF2_1 | 403 | 406 | PF00917 | 0.461 |
LIG_TRAF2_2 | 2 | 7 | PF00917 | 0.544 |
LIG_TRAF2_2 | 487 | 492 | PF00917 | 0.566 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.474 |
LIG_WRC_WIRS_1 | 716 | 721 | PF05994 | 0.692 |
LIG_WRPW_2 | 128 | 131 | PF00400 | 0.501 |
MOD_CDK_SPK_2 | 645 | 650 | PF00069 | 0.545 |
MOD_CDK_SPK_2 | 813 | 818 | PF00069 | 0.736 |
MOD_CDK_SPK_2 | 977 | 982 | PF00069 | 0.684 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.470 |
MOD_CDK_SPxxK_3 | 483 | 490 | PF00069 | 0.563 |
MOD_CDK_SPxxK_3 | 784 | 791 | PF00069 | 0.704 |
MOD_CDK_SPxxK_3 | 807 | 814 | PF00069 | 0.573 |
MOD_CK1_1 | 1053 | 1059 | PF00069 | 0.680 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.667 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.624 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.628 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.606 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.428 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.708 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.646 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.533 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.562 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.418 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.535 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.789 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.664 |
MOD_CK1_1 | 792 | 798 | PF00069 | 0.670 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.704 |
MOD_CK1_1 | 906 | 912 | PF00069 | 0.524 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.355 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.474 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.582 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.542 |
MOD_Cter_Amidation | 193 | 196 | PF01082 | 0.579 |
MOD_Cter_Amidation | 596 | 599 | PF01082 | 0.632 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.614 |
MOD_GlcNHglycan | 1059 | 1062 | PF01048 | 0.550 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.743 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.587 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.607 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.501 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.419 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.642 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.710 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.639 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.789 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.666 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.554 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.320 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.592 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.611 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.690 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.635 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.748 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.764 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.649 |
MOD_GlcNHglycan | 905 | 908 | PF01048 | 0.722 |
MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.651 |
MOD_GSK3_1 | 1053 | 1060 | PF00069 | 0.641 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.320 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.548 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.553 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.675 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.681 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.582 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.405 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.525 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.646 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.709 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.615 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.500 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.588 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.630 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.784 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.583 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.652 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.673 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.638 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.544 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.737 |
MOD_GSK3_1 | 809 | 816 | PF00069 | 0.694 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.737 |
MOD_GSK3_1 | 858 | 865 | PF00069 | 0.655 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.533 |
MOD_GSK3_1 | 867 | 874 | PF00069 | 0.672 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.650 |
MOD_GSK3_1 | 927 | 934 | PF00069 | 0.554 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.603 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.609 |
MOD_GSK3_1 | 992 | 999 | PF00069 | 0.590 |
MOD_LATS_1 | 95 | 101 | PF00433 | 0.543 |
MOD_N-GLC_1 | 1005 | 1010 | PF02516 | 0.568 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.751 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.305 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.803 |
MOD_N-GLC_1 | 645 | 650 | PF02516 | 0.578 |
MOD_N-GLC_1 | 726 | 731 | PF02516 | 0.521 |
MOD_N-GLC_1 | 755 | 760 | PF02516 | 0.671 |
MOD_N-GLC_1 | 789 | 794 | PF02516 | 0.743 |
MOD_N-GLC_1 | 956 | 961 | PF02516 | 0.580 |
MOD_NEK2_1 | 1004 | 1009 | PF00069 | 0.691 |
MOD_NEK2_1 | 1032 | 1037 | PF00069 | 0.674 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.537 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.495 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.399 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.449 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.396 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.560 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.482 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.458 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.671 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.593 |
MOD_NEK2_1 | 897 | 902 | PF00069 | 0.557 |
MOD_NEK2_1 | 973 | 978 | PF00069 | 0.632 |
MOD_PIKK_1 | 1053 | 1059 | PF00454 | 0.565 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.405 |
MOD_PK_1 | 553 | 559 | PF00069 | 0.450 |
MOD_PKA_1 | 752 | 758 | PF00069 | 0.698 |
MOD_PKA_2 | 1033 | 1039 | PF00069 | 0.700 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.386 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.690 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.663 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.615 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.681 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.673 |
MOD_PKB_1 | 195 | 203 | PF00069 | 0.548 |
MOD_PKB_1 | 923 | 931 | PF00069 | 0.694 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.444 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.309 |
MOD_Plk_1 | 974 | 980 | PF00069 | 0.625 |
MOD_Plk_4 | 1027 | 1033 | PF00069 | 0.560 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.456 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.525 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.405 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.444 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.309 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.426 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.588 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.612 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.673 |
MOD_ProDKin_1 | 1050 | 1056 | PF00069 | 0.724 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.328 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.524 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.573 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.587 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.463 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.640 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.561 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.639 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.569 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.700 |
MOD_ProDKin_1 | 784 | 790 | PF00069 | 0.701 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.767 |
MOD_ProDKin_1 | 977 | 983 | PF00069 | 0.599 |
MOD_SUMO_rev_2 | 335 | 342 | PF00179 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 1018 | 1021 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 751 | 753 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 913 | 915 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 923 | 926 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 937 | 940 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 948 | 950 | PF00400 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 351 | 355 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H6C9 | Leishmania donovani | 69% | 100% |
A4HTV6 | Leishmania infantum | 69% | 100% |
E9AMP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QHY2 | Leishmania major | 68% | 98% |