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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005783 | endoplasmic reticulum | 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:0000428 | DNA-directed RNA polymerase complex | 4 | 1 |
GO:0030880 | RNA polymerase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HHK2
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 10 |
GO:0006505 | GPI anchor metabolic process | 6 | 10 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 10 |
GO:0006629 | lipid metabolic process | 3 | 10 |
GO:0006643 | membrane lipid metabolic process | 4 | 10 |
GO:0006644 | phospholipid metabolic process | 4 | 10 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 10 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 10 |
GO:0006664 | glycolipid metabolic process | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008610 | lipid biosynthetic process | 4 | 10 |
GO:0008654 | phospholipid biosynthetic process | 5 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009247 | glycolipid biosynthetic process | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019637 | organophosphate metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 10 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 10 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 10 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 10 |
GO:0046486 | glycerolipid metabolic process | 4 | 10 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090407 | organophosphate biosynthetic process | 4 | 10 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 10 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
GO:1903509 | liposaccharide metabolic process | 4 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 1 |
GO:0097747 | RNA polymerase activity | 4 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.269 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.380 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.260 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.799 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.240 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.756 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 778 | 782 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 874 | 878 | PF00082 | 0.377 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 667 | 675 | PF00400 | 0.393 |
DEG_SCF_FBW7_2 | 867 | 873 | PF00400 | 0.656 |
DEG_SIAH_1 | 355 | 363 | PF03145 | 0.545 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.439 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.379 |
DOC_CKS1_1 | 867 | 872 | PF01111 | 0.652 |
DOC_CYCLIN_RxL_1 | 426 | 436 | PF00134 | 0.377 |
DOC_CYCLIN_RxL_1 | 665 | 672 | PF00134 | 0.393 |
DOC_CYCLIN_yClb1_LxF_4 | 361 | 366 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 746 | 752 | PF00134 | 0.335 |
DOC_CYCLIN_yCln2_LP_2 | 806 | 812 | PF00134 | 0.669 |
DOC_MAPK_FxFP_2 | 712 | 715 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 248 | 254 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 38 | 44 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 432 | 441 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 827 | 835 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 372 | 379 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 488 | 497 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 622 | 629 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 829 | 837 | PF00069 | 0.589 |
DOC_MAPK_NFAT4_5 | 622 | 630 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 361 | 367 | PF00149 | 0.458 |
DOC_PP1_RVXF_1 | 427 | 434 | PF00149 | 0.345 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 746 | 749 | PF13499 | 0.300 |
DOC_PP2B_LxvP_1 | 806 | 809 | PF13499 | 0.605 |
DOC_PP4_FxxP_1 | 712 | 715 | PF00568 | 0.300 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.561 |
DOC_USP7_UBL2_3 | 874 | 878 | PF12436 | 0.662 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.244 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 842 | 847 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 859 | 864 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 866 | 871 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 432 | 442 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 443 | 451 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 622 | 626 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 778 | 787 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 89 | 99 | PF00244 | 0.523 |
LIG_Actin_WH2_2 | 417 | 434 | PF00022 | 0.378 |
LIG_Actin_WH2_2 | 550 | 568 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 813 | 831 | PF00022 | 0.486 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.402 |
LIG_BRCT_BRCA1_1 | 691 | 695 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 710 | 714 | PF00533 | 0.157 |
LIG_BRCT_BRCA1_2 | 333 | 339 | PF00533 | 0.399 |
LIG_deltaCOP1_diTrp_1 | 559 | 567 | PF00928 | 0.525 |
LIG_DLG_GKlike_1 | 112 | 119 | PF00625 | 0.413 |
LIG_EH1_1 | 694 | 702 | PF00400 | 0.451 |
LIG_EH1_1 | 817 | 825 | PF00400 | 0.545 |
LIG_eIF4E_1 | 116 | 122 | PF01652 | 0.402 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.407 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.492 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.426 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.445 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.366 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.381 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.269 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.290 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.306 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.586 |
LIG_FHA_1 | 847 | 853 | PF00498 | 0.536 |
LIG_FHA_1 | 856 | 862 | PF00498 | 0.536 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.550 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.554 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.464 |
LIG_FHA_2 | 734 | 740 | PF00498 | 0.325 |
LIG_GBD_Chelix_1 | 820 | 828 | PF00786 | 0.267 |
LIG_IRF3_LxIS_1 | 149 | 156 | PF10401 | 0.341 |
LIG_LIR_Apic_2 | 711 | 715 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 559 | 569 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 619 | 627 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 704 | 715 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 740 | 751 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 815 | 826 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 619 | 623 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 672 | 678 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 704 | 710 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 711 | 717 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 740 | 746 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 815 | 821 | PF02991 | 0.486 |
LIG_LYPXL_SIV_4 | 663 | 671 | PF13949 | 0.393 |
LIG_NRBOX | 426 | 432 | PF00104 | 0.304 |
LIG_Pex14_1 | 532 | 536 | PF04695 | 0.490 |
LIG_PTB_Apo_2 | 473 | 480 | PF02174 | 0.186 |
LIG_PTB_Phospho_1 | 473 | 479 | PF10480 | 0.186 |
LIG_REV1ctd_RIR_1 | 550 | 559 | PF16727 | 0.459 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.233 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.458 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.435 |
LIG_SH2_GRB2like | 474 | 477 | PF00017 | 0.186 |
LIG_SH2_GRB2like | 588 | 591 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 41 | 44 | PF00017 | 0.419 |
LIG_SH2_PTP2 | 479 | 482 | PF00017 | 0.325 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.441 |
LIG_SH2_SRC | 423 | 426 | PF00017 | 0.371 |
LIG_SH2_SRC | 588 | 591 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 693 | 696 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 743 | 746 | PF00017 | 0.310 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.360 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.482 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.460 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.618 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.474 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.242 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.238 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.437 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.335 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.479 |
LIG_SUMO_SIM_anti_2 | 80 | 86 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 831 | 837 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 556 | 562 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 796 | 802 | PF11976 | 0.600 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.401 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.263 |
LIG_TRAF2_1 | 789 | 792 | PF00917 | 0.562 |
LIG_TRAF2_2 | 348 | 353 | PF00917 | 0.423 |
LIG_TYR_ITIM | 498 | 503 | PF00017 | 0.393 |
LIG_TYR_ITIM | 681 | 686 | PF00017 | 0.522 |
LIG_TYR_ITIM | 741 | 746 | PF00017 | 0.393 |
LIG_UBA3_1 | 427 | 435 | PF00899 | 0.295 |
LIG_UBA3_1 | 824 | 832 | PF00899 | 0.581 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 709 | 714 | PF05994 | 0.433 |
LIG_WW_3 | 360 | 364 | PF00397 | 0.485 |
MOD_CDK_SPK_2 | 842 | 847 | PF00069 | 0.558 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.497 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.472 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.422 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.414 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.413 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.498 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.531 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.558 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.593 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.284 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.607 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.384 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.499 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.419 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.498 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.414 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.549 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.554 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.402 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.460 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.325 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.642 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.476 |
MOD_Cter_Amidation | 246 | 249 | PF01082 | 0.598 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.629 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.620 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.649 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.622 |
MOD_GlcNHglycan | 301 | 305 | PF01048 | 0.800 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.686 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.383 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.371 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.437 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.460 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.515 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.403 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.506 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.585 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.460 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.259 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.361 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.551 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.539 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.618 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.509 |
MOD_GSK3_1 | 842 | 849 | PF00069 | 0.627 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.547 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.496 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.704 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.618 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.709 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.718 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.611 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.606 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.238 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.467 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.397 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.512 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.389 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.364 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.315 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.376 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.426 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.506 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.289 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.276 |
MOD_NEK2_2 | 647 | 652 | PF00069 | 0.325 |
MOD_NEK2_2 | 742 | 747 | PF00069 | 0.388 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.311 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.419 |
MOD_PK_1 | 151 | 157 | PF00069 | 0.477 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.418 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.313 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.365 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.563 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.508 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.557 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.424 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.405 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.383 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.395 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.438 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.506 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.358 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.445 |
MOD_PKB_1 | 687 | 695 | PF00069 | 0.405 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.488 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.521 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.372 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.467 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.511 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.408 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.538 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.407 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.482 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.571 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.408 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.390 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.399 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.512 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.492 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.448 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.331 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.599 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.276 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.294 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.460 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.460 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.355 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.436 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.416 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.244 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.528 |
MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.530 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.541 |
MOD_ProDKin_1 | 842 | 848 | PF00069 | 0.550 |
MOD_ProDKin_1 | 859 | 865 | PF00069 | 0.680 |
MOD_ProDKin_1 | 866 | 872 | PF00069 | 0.676 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.373 |
MOD_SUMO_for_1 | 56 | 59 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 54 | 58 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 374 | 379 | PF01217 | 0.391 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_2 | 445 | 451 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.206 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 743 | 746 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.230 |
TRG_ER_diArg_1 | 686 | 689 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 827 | 830 | PF00400 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.669 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C0 | Leptomonas seymouri | 64% | 98% |
A0A0S4IQS6 | Bodo saltans | 26% | 100% |
A0A3Q8IEF3 | Leishmania donovani | 78% | 100% |
A0A3S5IRD9 | Trypanosoma rangeli | 31% | 100% |
E9AE65 | Leishmania major | 77% | 100% |
E9AHJ3 | Leishmania infantum | 78% | 100% |
E9ALM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
V5BBW4 | Trypanosoma cruzi | 32% | 100% |