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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APJ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 6 |
GO:0006644 | phospholipid metabolic process | 4 | 6 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 6 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0007165 | signal transduction | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 6 |
GO:0008654 | phospholipid biosynthetic process | 5 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044255 | cellular lipid metabolic process | 3 | 6 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 6 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 6 |
GO:0046486 | glycerolipid metabolic process | 4 | 6 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 6 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 6 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 8 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090407 | organophosphate biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0016303 | 1-phosphatidylinositol-3-kinase activity | 6 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 2 |
GO:0035004 | phosphatidylinositol 3-kinase activity | 5 | 2 |
GO:0052742 | phosphatidylinositol kinase activity | 5 | 2 |
GO:0046934 | phosphatidylinositol-4,5-bisphosphate 3-kinase activity | 6 | 1 |
GO:0052812 | phosphatidylinositol-3,4-bisphosphate 5-kinase activity | 6 | 1 |
GO:0052813 | phosphatidylinositol bisphosphate kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.287 |
CLV_C14_Caspase3-7 | 702 | 706 | PF00656 | 0.246 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 902 | 904 | PF00675 | 0.212 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 902 | 904 | PF00082 | 0.212 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 832 | 834 | PF00082 | 0.251 |
CLV_PCSK_PC7_1 | 546 | 552 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 902 | 906 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 930 | 934 | PF00082 | 0.328 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.317 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.337 |
DOC_ANK_TNKS_1 | 356 | 363 | PF00023 | 0.319 |
DOC_CKS1_1 | 839 | 844 | PF01111 | 0.446 |
DOC_CYCLIN_RxL_1 | 277 | 287 | PF00134 | 0.264 |
DOC_CYCLIN_RxL_1 | 540 | 552 | PF00134 | 0.246 |
DOC_CYCLIN_RxL_1 | 900 | 911 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 355 | 363 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 663 | 671 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 34 | 41 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 663 | 671 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 692 | 700 | PF00069 | 0.261 |
DOC_MAPK_MEF2A_6 | 709 | 717 | PF00069 | 0.193 |
DOC_MAPK_NFAT4_5 | 34 | 42 | PF00069 | 0.415 |
DOC_PP1_RVXF_1 | 258 | 264 | PF00149 | 0.268 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.221 |
DOC_PP1_RVXF_1 | 281 | 287 | PF00149 | 0.310 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.379 |
DOC_PP1_RVXF_1 | 442 | 449 | PF00149 | 0.264 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.438 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.325 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.331 |
DOC_SPAK_OSR1_1 | 680 | 684 | PF12202 | 0.197 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.403 |
DOC_USP7_UBL2_3 | 459 | 463 | PF12436 | 0.287 |
DOC_USP7_UBL2_3 | 609 | 613 | PF12436 | 0.277 |
DOC_USP7_UBL2_3 | 620 | 624 | PF12436 | 0.309 |
DOC_USP7_UBL2_3 | 828 | 832 | PF12436 | 0.446 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.246 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 838 | 843 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 850 | 855 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 550 | 554 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 627 | 631 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 638 | 642 | PF00244 | 0.220 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 86 | 96 | PF00244 | 0.191 |
LIG_14-3-3_CanoR_1 | 871 | 881 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 182 | 198 | PF00022 | 0.214 |
LIG_Actin_WH2_2 | 414 | 430 | PF00022 | 0.297 |
LIG_Actin_WH2_2 | 888 | 904 | PF00022 | 0.493 |
LIG_AP2alpha_1 | 635 | 639 | PF02296 | 0.214 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_1 | 661 | 665 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 852 | 856 | PF00533 | 0.537 |
LIG_Clathr_ClatBox_1 | 471 | 475 | PF01394 | 0.337 |
LIG_Clathr_ClatBox_1 | 813 | 817 | PF01394 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 3 | 7 | PF00928 | 0.372 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.246 |
LIG_eIF4E_1 | 477 | 483 | PF01652 | 0.264 |
LIG_eIF4E_1 | 602 | 608 | PF01652 | 0.271 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.337 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.311 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.436 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.337 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.339 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.269 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.246 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.299 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.298 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.169 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.337 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.287 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.301 |
LIG_FHA_2 | 892 | 898 | PF00498 | 0.563 |
LIG_FHA_2 | 908 | 914 | PF00498 | 0.474 |
LIG_Integrin_RGD_1 | 50 | 52 | PF01839 | 0.516 |
LIG_IRF3_LxIS_1 | 201 | 207 | PF10401 | 0.388 |
LIG_LIR_Apic_2 | 152 | 157 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 337 | 346 | PF02991 | 0.170 |
LIG_LIR_Gen_1 | 499 | 507 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 538 | 549 | PF02991 | 0.170 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 678 | 685 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 935 | 941 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 94 | 100 | PF02991 | 0.337 |
LIG_LIR_LC3C_4 | 504 | 507 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 817 | 821 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 853 | 859 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 915 | 921 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 935 | 939 | PF02991 | 0.371 |
LIG_MLH1_MIPbox_1 | 323 | 327 | PF16413 | 0.337 |
LIG_PCNA_APIM_2 | 544 | 550 | PF02747 | 0.246 |
LIG_PCNA_yPIPBox_3 | 550 | 563 | PF02747 | 0.319 |
LIG_Pex14_1 | 470 | 474 | PF04695 | 0.246 |
LIG_Pex14_1 | 763 | 767 | PF04695 | 0.246 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.319 |
LIG_Pex14_2 | 635 | 639 | PF04695 | 0.362 |
LIG_Pex14_2 | 681 | 685 | PF04695 | 0.258 |
LIG_Pex14_2 | 814 | 818 | PF04695 | 0.446 |
LIG_Pex14_2 | 821 | 825 | PF04695 | 0.446 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.277 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.319 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.287 |
LIG_SH2_CRK | 720 | 724 | PF00017 | 0.246 |
LIG_SH2_CRK | 867 | 871 | PF00017 | 0.486 |
LIG_SH2_CRK | 918 | 922 | PF00017 | 0.551 |
LIG_SH2_NCK_1 | 788 | 792 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 936 | 939 | PF00017 | 0.506 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.246 |
LIG_SH2_SRC | 844 | 847 | PF00017 | 0.519 |
LIG_SH2_SRC | 936 | 939 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 597 | 600 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.170 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 788 | 791 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 844 | 847 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 858 | 861 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 936 | 939 | PF00017 | 0.494 |
LIG_SH3_2 | 12 | 17 | PF14604 | 0.484 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.305 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.205 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.336 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.280 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.470 |
LIG_SH3_4 | 317 | 324 | PF00018 | 0.170 |
LIG_SUMO_SIM_anti_2 | 141 | 147 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 493 | 499 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 881 | 887 | PF11976 | 0.446 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.263 |
LIG_TRAF2_1 | 910 | 913 | PF00917 | 0.501 |
LIG_TYR_ITIM | 431 | 436 | PF00017 | 0.400 |
LIG_TYR_ITIM | 718 | 723 | PF00017 | 0.324 |
LIG_UBA3_1 | 527 | 535 | PF00899 | 0.393 |
LIG_UBA3_1 | 583 | 589 | PF00899 | 0.363 |
LIG_UBA3_1 | 700 | 709 | PF00899 | 0.299 |
LIG_WW_2 | 30 | 33 | PF00397 | 0.302 |
MOD_CDC14_SPxK_1 | 591 | 594 | PF00782 | 0.465 |
MOD_CDK_SPxK_1 | 588 | 594 | PF00069 | 0.400 |
MOD_CDK_SPxxK_3 | 850 | 857 | PF00069 | 0.400 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.620 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.250 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.284 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.310 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.495 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.563 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.591 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.348 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.316 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.515 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.299 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.305 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.356 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.400 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.192 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.425 |
MOD_CK2_1 | 907 | 913 | PF00069 | 0.382 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.550 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.499 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.388 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.299 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.400 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.425 |
MOD_GlcNHglycan | 874 | 877 | PF01048 | 0.425 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.594 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.365 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.157 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.299 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.482 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.363 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.192 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.545 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.336 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.299 |
MOD_N-GLC_1 | 742 | 747 | PF02516 | 0.299 |
MOD_N-GLC_1 | 907 | 912 | PF02516 | 0.453 |
MOD_N-GLC_2 | 371 | 373 | PF02516 | 0.515 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.525 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.311 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.356 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.299 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.501 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.223 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.299 |
MOD_NEK2_1 | 781 | 786 | PF00069 | 0.299 |
MOD_NEK2_1 | 848 | 853 | PF00069 | 0.387 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.321 |
MOD_NEK2_1 | 883 | 888 | PF00069 | 0.309 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.500 |
MOD_NEK2_2 | 866 | 871 | PF00069 | 0.192 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.372 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.425 |
MOD_PKA_1 | 832 | 838 | PF00069 | 0.299 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.571 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.511 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.373 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.324 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.416 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.272 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.559 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.299 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.222 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.495 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.366 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.300 |
MOD_Plk_2-3 | 516 | 522 | PF00069 | 0.400 |
MOD_Plk_2-3 | 891 | 897 | PF00069 | 0.470 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.463 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.495 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.449 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.457 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.299 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.299 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.115 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.192 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.397 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.400 |
MOD_ProDKin_1 | 838 | 844 | PF00069 | 0.285 |
MOD_ProDKin_1 | 850 | 856 | PF00069 | 0.290 |
MOD_SUMO_for_1 | 211 | 214 | PF00179 | 0.412 |
MOD_SUMO_for_1 | 534 | 537 | PF00179 | 0.299 |
MOD_SUMO_for_1 | 831 | 834 | PF00179 | 0.299 |
MOD_SUMO_for_1 | 96 | 99 | PF00179 | 0.192 |
MOD_SUMO_rev_2 | 141 | 151 | PF00179 | 0.425 |
MOD_SUMO_rev_2 | 441 | 446 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 653 | 660 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 94 | 102 | PF00179 | 0.192 |
TRG_DiLeu_BaEn_1 | 478 | 483 | PF01217 | 0.324 |
TRG_DiLeu_BaEn_1 | 578 | 583 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_2 | 833 | 839 | PF01217 | 0.299 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.204 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 720 | 723 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 867 | 870 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 918 | 921 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 936 | 939 | PF00928 | 0.233 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 549 | 551 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 901 | 903 | PF00400 | 0.249 |
TRG_NES_CRM1_1 | 422 | 434 | PF08389 | 0.425 |
TRG_NES_CRM1_1 | 522 | 537 | PF08389 | 0.324 |
TRG_NES_CRM1_1 | 689 | 702 | PF08389 | 0.299 |
TRG_NES_CRM1_1 | 896 | 911 | PF08389 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.209 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 429 | 434 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 930 | 935 | PF00026 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0G2K344 | Rattus norvegicus | 33% | 88% |
A0A0N1I4K0 | Leptomonas seymouri | 75% | 90% |
A0A1X0NPD0 | Trypanosomatidae | 56% | 89% |
A0A3R7MRK8 | Trypanosoma rangeli | 54% | 89% |
A0A3S7WSQ8 | Leishmania donovani | 89% | 90% |
A4HVU4 | Leishmania infantum | 89% | 90% |
O00329 | Homo sapiens | 34% | 90% |
O02697 | Sus scrofa | 33% | 85% |
O35904 | Mus musculus | 34% | 90% |
P0C5E7 | Caenorhabditis briggsae | 28% | 81% |
P32871 | Bos taurus | 33% | 88% |
P42336 | Homo sapiens | 33% | 88% |
P42337 | Mus musculus | 33% | 88% |
P42338 | Homo sapiens | 35% | 88% |
P48736 | Homo sapiens | 34% | 85% |
Q8BTI9 | Mus musculus | 35% | 89% |
Q94125 | Caenorhabditis elegans | 28% | 80% |
Q9JHG7 | Mus musculus | 33% | 85% |
Q9Z1L0 | Rattus norvegicus | 34% | 88% |
V5AXQ0 | Trypanosoma cruzi | 54% | 89% |