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 | 2 |
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: Q4QBN2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 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:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
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 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
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:0140096 | catalytic activity, acting on a protein | 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 | 986 | 990 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 1007 | 1009 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 1012 | 1014 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 1041 | 1043 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 1052 | 1054 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.763 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 878 | 880 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 933 | 935 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 971 | 973 | PF00675 | 0.739 |
CLV_PCSK_FUR_1 | 1037 | 1041 | PF00082 | 0.422 |
CLV_PCSK_FUR_1 | 1050 | 1054 | PF00082 | 0.320 |
CLV_PCSK_FUR_1 | 620 | 624 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 1007 | 1009 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 1012 | 1014 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 1039 | 1041 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 1052 | 1054 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 877 | 879 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 932 | 934 | PF00082 | 0.798 |
CLV_PCSK_KEX2_1 | 971 | 973 | PF00082 | 0.739 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.736 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 715 | 717 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 877 | 879 | PF00082 | 0.751 |
CLV_PCSK_PC7_1 | 1008 | 1014 | PF00082 | 0.741 |
CLV_PCSK_PC7_1 | 1037 | 1043 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 729 | 735 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 674 | 678 | PF00082 | 0.668 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.517 |
DEG_APCC_DBOX_1 | 551 | 559 | PF00400 | 0.426 |
DEG_APCC_DBOX_1 | 682 | 690 | PF00400 | 0.372 |
DEG_APCC_DBOX_1 | 715 | 723 | PF00400 | 0.372 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.526 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.441 |
DOC_CDC14_PxL_1 | 612 | 620 | PF14671 | 0.367 |
DOC_CKS1_1 | 964 | 969 | PF01111 | 0.427 |
DOC_CYCLIN_RxL_1 | 546 | 559 | PF00134 | 0.462 |
DOC_CYCLIN_RxL_1 | 910 | 921 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.486 |
DOC_MAPK_DCC_7 | 138 | 147 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 282 | 292 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 38 | 48 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 285 | 292 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 683 | 692 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 698 | 706 | PF00069 | 0.426 |
DOC_MAPK_NFAT4_5 | 683 | 691 | PF00069 | 0.368 |
DOC_MAPK_RevD_3 | 1025 | 1040 | PF00069 | 0.388 |
DOC_PP1_RVXF_1 | 42 | 49 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 1003 | 1006 | PF13499 | 0.577 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 866 | 869 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 917 | 920 | PF13499 | 0.482 |
DOC_USP7_MATH_1 | 1020 | 1024 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 905 | 909 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 955 | 959 | PF00917 | 0.509 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 819 | 824 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 825 | 830 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 857 | 862 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 881 | 886 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 963 | 968 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 971 | 976 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 988 | 993 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 1012 | 1020 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 1022 | 1026 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 246 | 256 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 346 | 354 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 38 | 48 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 626 | 631 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 659 | 663 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 698 | 703 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 716 | 720 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 733 | 739 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 816 | 823 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 839 | 844 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 142 | 160 | PF00022 | 0.480 |
LIG_Actin_WH2_2 | 319 | 337 | PF00022 | 0.424 |
LIG_APCC_ABBA_1 | 118 | 123 | PF00400 | 0.539 |
LIG_BIR_III_2 | 989 | 993 | PF00653 | 0.481 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.475 |
LIG_Clathr_ClatBox_1 | 555 | 559 | PF01394 | 0.428 |
LIG_deltaCOP1_diTrp_1 | 273 | 283 | PF00928 | 0.429 |
LIG_eIF4E_1 | 601 | 607 | PF01652 | 0.315 |
LIG_EVH1_1 | 615 | 619 | PF00568 | 0.392 |
LIG_FHA_1 | 1043 | 1049 | PF00498 | 0.623 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.450 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.473 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.377 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.452 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.350 |
LIG_FHA_1 | 912 | 918 | PF00498 | 0.486 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.439 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.359 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.419 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.475 |
LIG_FHA_2 | 754 | 760 | PF00498 | 0.436 |
LIG_FHA_2 | 924 | 930 | PF00498 | 0.493 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.441 |
LIG_FHA_2 | 984 | 990 | PF00498 | 0.567 |
LIG_LIR_Apic_2 | 1015 | 1020 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 926 | 931 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 273 | 281 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.534 |
LIG_MYND_1 | 825 | 829 | PF01753 | 0.516 |
LIG_NRBOX | 602 | 608 | PF00104 | 0.316 |
LIG_NRP_CendR_1 | 1053 | 1056 | PF00754 | 0.449 |
LIG_PCNA_PIPBox_1 | 670 | 679 | PF02747 | 0.368 |
LIG_PCNA_yPIPBox_3 | 640 | 654 | PF02747 | 0.382 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.520 |
LIG_PTB_Apo_2 | 533 | 540 | PF02174 | 0.400 |
LIG_PTB_Phospho_1 | 533 | 539 | PF10480 | 0.399 |
LIG_REV1ctd_RIR_1 | 725 | 733 | PF16727 | 0.385 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.345 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.421 |
LIG_SH2_CRK | 928 | 932 | PF00017 | 0.492 |
LIG_SH2_NCK_1 | 167 | 171 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 654 | 658 | PF00017 | 0.373 |
LIG_SH2_PTP2 | 478 | 481 | PF00017 | 0.535 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 654 | 658 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 1026 | 1029 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.503 |
LIG_SH3_2 | 464 | 469 | PF14604 | 0.444 |
LIG_SH3_3 | 1003 | 1009 | PF00018 | 0.519 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.534 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.478 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.482 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.529 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.469 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.439 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.433 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.380 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.561 |
LIG_SH3_3 | 802 | 808 | PF00018 | 0.430 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.577 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.523 |
LIG_SH3_3 | 961 | 967 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 1029 | 1034 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 162 | 168 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 554 | 562 | PF11976 | 0.402 |
LIG_TRAF2_1 | 849 | 852 | PF00917 | 0.532 |
LIG_TRAF2_1 | 893 | 896 | PF00917 | 0.563 |
LIG_TRAF2_2 | 440 | 445 | PF00917 | 0.406 |
LIG_TRFH_1 | 48 | 52 | PF08558 | 0.656 |
LIG_TYR_ITIM | 606 | 611 | PF00017 | 0.521 |
LIG_UBA3_1 | 669 | 674 | PF00899 | 0.492 |
LIG_WW_2 | 616 | 619 | PF00397 | 0.487 |
MOD_CDC14_SPxK_1 | 180 | 183 | PF00782 | 0.638 |
MOD_CDK_SPK_2 | 177 | 182 | PF00069 | 0.633 |
MOD_CDK_SPxK_1 | 177 | 183 | PF00069 | 0.636 |
MOD_CDK_SPxK_1 | 810 | 816 | PF00069 | 0.580 |
MOD_CDK_SPxxK_3 | 177 | 184 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 971 | 978 | PF00069 | 0.601 |
MOD_CDK_SPxxK_3 | 988 | 995 | PF00069 | 0.605 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.585 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.640 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.685 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.521 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.536 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.612 |
MOD_CK1_1 | 815 | 821 | PF00069 | 0.827 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.636 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.605 |
MOD_CK1_1 | 884 | 890 | PF00069 | 0.686 |
MOD_CK1_1 | 918 | 924 | PF00069 | 0.759 |
MOD_CK1_1 | 948 | 954 | PF00069 | 0.700 |
MOD_CK1_1 | 957 | 963 | PF00069 | 0.652 |
MOD_CK1_1 | 981 | 987 | PF00069 | 0.635 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.655 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.515 |
MOD_CK2_1 | 845 | 851 | PF00069 | 0.643 |
MOD_Cter_Amidation | 36 | 39 | PF01082 | 0.560 |
MOD_Cter_Amidation | 731 | 734 | PF01082 | 0.544 |
MOD_DYRK1A_RPxSP_1 | 788 | 792 | PF00069 | 0.642 |
MOD_GlcNHglycan | 1014 | 1017 | PF01048 | 0.684 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.653 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.602 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.647 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.554 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.511 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.491 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.704 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.615 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.668 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.665 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.639 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.551 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.377 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.591 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.670 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.606 |
MOD_GlcNHglycan | 838 | 842 | PF01048 | 0.650 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.639 |
MOD_GlcNHglycan | 917 | 920 | PF01048 | 0.621 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.666 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.607 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.609 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.668 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.545 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.660 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.543 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.517 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.519 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.521 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.660 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.621 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.666 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.728 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.737 |
MOD_GSK3_1 | 911 | 918 | PF00069 | 0.638 |
MOD_GSK3_1 | 951 | 958 | PF00069 | 0.737 |
MOD_GSK3_1 | 984 | 991 | PF00069 | 0.669 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.568 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.655 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.570 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.715 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.340 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.599 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.543 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.566 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.694 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.556 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.706 |
MOD_NEK2_1 | 915 | 920 | PF00069 | 0.607 |
MOD_NEK2_1 | 923 | 928 | PF00069 | 0.638 |
MOD_NEK2_1 | 945 | 950 | PF00069 | 0.675 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.657 |
MOD_NEK2_2 | 658 | 663 | PF00069 | 0.506 |
MOD_NEK2_2 | 999 | 1004 | PF00069 | 0.585 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.628 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.374 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.526 |
MOD_PIKK_1 | 981 | 987 | PF00454 | 0.636 |
MOD_PK_1 | 933 | 939 | PF00069 | 0.718 |
MOD_PK_1 | 978 | 984 | PF00069 | 0.559 |
MOD_PKA_1 | 1012 | 1018 | PF00069 | 0.679 |
MOD_PKA_1 | 622 | 628 | PF00069 | 0.620 |
MOD_PKA_1 | 715 | 721 | PF00069 | 0.524 |
MOD_PKA_1 | 734 | 740 | PF00069 | 0.350 |
MOD_PKA_1 | 878 | 884 | PF00069 | 0.655 |
MOD_PKA_1 | 933 | 939 | PF00069 | 0.686 |
MOD_PKA_2 | 1012 | 1018 | PF00069 | 0.699 |
MOD_PKA_2 | 1021 | 1027 | PF00069 | 0.394 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.695 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.617 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.658 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.620 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.537 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.606 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.338 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.502 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.700 |
MOD_PKA_2 | 878 | 884 | PF00069 | 0.631 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.607 |
MOD_PKA_2 | 933 | 939 | PF00069 | 0.686 |
MOD_PKB_1 | 1040 | 1048 | PF00069 | 0.470 |
MOD_PKB_1 | 182 | 190 | PF00069 | 0.618 |
MOD_PKB_1 | 246 | 254 | PF00069 | 0.615 |
MOD_PKB_1 | 620 | 628 | PF00069 | 0.611 |
MOD_Plk_1 | 1042 | 1048 | PF00069 | 0.517 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.610 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.566 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.460 |
MOD_Plk_1 | 879 | 885 | PF00069 | 0.697 |
MOD_Plk_1 | 978 | 984 | PF00069 | 0.638 |
MOD_Plk_4 | 1021 | 1027 | PF00069 | 0.427 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.562 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.654 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.675 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.625 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.655 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.636 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.598 |
MOD_Plk_4 | 905 | 911 | PF00069 | 0.769 |
MOD_Plk_4 | 918 | 924 | PF00069 | 0.725 |
MOD_Plk_4 | 978 | 984 | PF00069 | 0.599 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.636 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.583 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.406 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.510 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.511 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.812 |
MOD_ProDKin_1 | 810 | 816 | PF00069 | 0.589 |
MOD_ProDKin_1 | 819 | 825 | PF00069 | 0.617 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.694 |
MOD_ProDKin_1 | 857 | 863 | PF00069 | 0.699 |
MOD_ProDKin_1 | 881 | 887 | PF00069 | 0.691 |
MOD_ProDKin_1 | 963 | 969 | PF00069 | 0.708 |
MOD_ProDKin_1 | 971 | 977 | PF00069 | 0.710 |
MOD_ProDKin_1 | 988 | 994 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 667 | 676 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_1 | 1043 | 1048 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 551 | 556 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_2 | 671 | 677 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.588 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 1006 | 1008 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 1011 | 1013 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 1036 | 1039 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 1040 | 1042 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 1050 | 1053 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 621 | 623 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 733 | 735 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 747 | 749 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 769 | 772 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 931 | 934 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 970 | 972 | PF00400 | 0.679 |
TRG_NLS_Bipartite_1 | 327 | 348 | PF00514 | 0.478 |
TRG_NLS_MonoExtC_3 | 467 | 472 | PF00514 | 0.529 |
TRG_NLS_MonoExtN_4 | 181 | 186 | PF00514 | 0.626 |
TRG_NLS_MonoExtN_4 | 342 | 348 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 467 | 472 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 943 | 947 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDS2 | Leptomonas seymouri | 38% | 100% |
A0A3Q8IEB0 | Leishmania donovani | 92% | 100% |
A4HCF5 | Leishmania braziliensis | 72% | 100% |
A4HZY6 | Leishmania infantum | 92% | 100% |
E9AVU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |