Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005634 | nucleus | 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 |
Related structures:
AlphaFold database: A4HEE3
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031056 | regulation of histone modification | 7 | 1 |
GO:0031058 | obsolete positive regulation of histone modification | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0035065 | regulation of histone acetylation | 8 | 1 |
GO:0035066 | positive regulation of histone acetylation | 9 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901983 | regulation of protein acetylation | 7 | 1 |
GO:1901985 | positive regulation of protein acetylation | 8 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2000756 | regulation of peptidyl-lysine acetylation | 8 | 1 |
GO:2000758 | positive regulation of peptidyl-lysine acetylation | 9 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003713 | transcription coactivator activity | 3 | 1 |
GO:0005488 | binding | 1 | 2 |
GO:0140110 | transcription regulator activity | 1 | 1 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0003777 | microtubule motor activity | 2 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.299 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.372 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 842 | 844 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 417 | 421 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 719 | 721 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 842 | 844 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 419 | 421 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.432 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 842 | 846 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 848 | 852 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 666 | 674 | PF00400 | 0.384 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.385 |
DOC_CYCLIN_RxL_1 | 544 | 552 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 277 | 285 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 495 | 503 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 746 | 755 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 759 | 765 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 885 | 893 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 155 | 162 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 277 | 285 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 746 | 755 | PF00069 | 0.467 |
DOC_PP2B_LxvP_1 | 281 | 284 | PF13499 | 0.461 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.548 |
DOC_USP7_MATH_2 | 624 | 630 | PF00917 | 0.594 |
DOC_USP7_UBL2_3 | 183 | 187 | PF12436 | 0.354 |
DOC_USP7_UBL2_3 | 429 | 433 | PF12436 | 0.540 |
DOC_USP7_UBL2_3 | 584 | 588 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 711 | 715 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 799 | 804 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 891 | 896 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 264 | 273 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 819 | 825 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 888 | 894 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 933 | 941 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 942 | 946 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 688 | 706 | PF00022 | 0.439 |
LIG_APCC_ABBA_1 | 763 | 768 | PF00400 | 0.558 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.390 |
LIG_Clathr_ClatBox_1 | 614 | 618 | PF01394 | 0.538 |
LIG_deltaCOP1_diTrp_1 | 360 | 369 | PF00928 | 0.545 |
LIG_eIF4E_1 | 811 | 817 | PF01652 | 0.417 |
LIG_eIF4E_1 | 945 | 951 | PF01652 | 0.265 |
LIG_EVH1_2 | 907 | 911 | PF00568 | 0.389 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.329 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.573 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.480 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.397 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.587 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.550 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.450 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.502 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.470 |
LIG_FHA_1 | 922 | 928 | PF00498 | 0.432 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.488 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.429 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.468 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.498 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.491 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.483 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.517 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.497 |
LIG_FHA_2 | 830 | 836 | PF00498 | 0.407 |
LIG_FHA_2 | 847 | 853 | PF00498 | 0.477 |
LIG_FHA_2 | 926 | 932 | PF00498 | 0.362 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 186 | 193 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 767 | 776 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 924 | 934 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 944 | 955 | PF02991 | 0.236 |
LIG_LIR_LC3C_4 | 373 | 377 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 767 | 773 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 875 | 881 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 924 | 929 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 944 | 950 | PF02991 | 0.214 |
LIG_MAD2 | 853 | 861 | PF02301 | 0.413 |
LIG_NRBOX | 840 | 846 | PF00104 | 0.397 |
LIG_PCNA_yPIPBox_3 | 50 | 59 | PF02747 | 0.490 |
LIG_Pex14_2 | 634 | 638 | PF04695 | 0.534 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.368 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.369 |
LIG_SH2_CRK | 947 | 951 | PF00017 | 0.419 |
LIG_SH2_CRK | 953 | 957 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 332 | 335 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 306 | 310 | PF00017 | 0.560 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 766 | 770 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 930 | 934 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 947 | 951 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 949 | 952 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 945 | 948 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.299 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.569 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.607 |
LIG_SH3_3 | 867 | 873 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 823 | 833 | PF11976 | 0.405 |
LIG_SUMO_SIM_anti_2 | 935 | 944 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 613 | 619 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 751 | 757 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 843 | 849 | PF11976 | 0.318 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.644 |
LIG_TRAF2_1 | 509 | 512 | PF00917 | 0.547 |
LIG_TRAF2_1 | 591 | 594 | PF00917 | 0.602 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.549 |
LIG_TRAF2_1 | 894 | 897 | PF00917 | 0.486 |
LIG_TYR_ITIM | 951 | 956 | PF00017 | 0.309 |
LIG_UBA3_1 | 353 | 361 | PF00899 | 0.676 |
LIG_UBA3_1 | 754 | 760 | PF00899 | 0.450 |
LIG_UBA3_1 | 844 | 848 | PF00899 | 0.470 |
LIG_WRC_WIRS_1 | 770 | 775 | PF05994 | 0.509 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.413 |
MOD_CDK_SPxK_1 | 90 | 96 | PF00069 | 0.413 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.638 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.524 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.388 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.423 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.530 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.534 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.612 |
MOD_CK1_1 | 846 | 852 | PF00069 | 0.568 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.527 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.518 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.627 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.558 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.379 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.558 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.504 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.486 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.581 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.396 |
MOD_CK2_1 | 846 | 852 | PF00069 | 0.409 |
MOD_CK2_1 | 891 | 897 | PF00069 | 0.467 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.480 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.562 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.588 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.428 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.399 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.574 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.621 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.531 |
MOD_GlcNHglycan | 504 | 510 | PF01048 | 0.447 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.571 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.602 |
MOD_GlcNHglycan | 935 | 938 | PF01048 | 0.395 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.501 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.433 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.539 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.550 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.501 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.633 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.543 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.372 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.526 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.585 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.467 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.499 |
MOD_GSK3_1 | 921 | 928 | PF00069 | 0.428 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.340 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.536 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.655 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.608 |
MOD_N-GLC_1 | 789 | 794 | PF02516 | 0.592 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.354 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.540 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.587 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.643 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.546 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.417 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.599 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.617 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.517 |
MOD_NEK2_1 | 940 | 945 | PF00069 | 0.350 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.357 |
MOD_NEK2_2 | 925 | 930 | PF00069 | 0.416 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.304 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.639 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.404 |
MOD_PIKK_1 | 636 | 642 | PF00454 | 0.447 |
MOD_PIKK_1 | 678 | 684 | PF00454 | 0.560 |
MOD_PIKK_1 | 774 | 780 | PF00454 | 0.604 |
MOD_PIKK_1 | 795 | 801 | PF00454 | 0.515 |
MOD_PK_1 | 420 | 426 | PF00069 | 0.563 |
MOD_PK_1 | 452 | 458 | PF00069 | 0.555 |
MOD_PK_1 | 843 | 849 | PF00069 | 0.318 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.468 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.457 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.391 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.474 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.468 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.457 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.347 |
MOD_PKA_2 | 932 | 938 | PF00069 | 0.396 |
MOD_PKA_2 | 941 | 947 | PF00069 | 0.402 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.473 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.399 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.492 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.542 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.401 |
MOD_Plk_1 | 896 | 902 | PF00069 | 0.497 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.350 |
MOD_Plk_2-3 | 603 | 609 | PF00069 | 0.476 |
MOD_Plk_2-3 | 829 | 835 | PF00069 | 0.308 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.370 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.398 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.537 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.423 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.469 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.494 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.533 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.440 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.406 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.450 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.452 |
MOD_Plk_4 | 941 | 947 | PF00069 | 0.505 |
MOD_ProDKin_1 | 799 | 805 | PF00069 | 0.470 |
MOD_ProDKin_1 | 891 | 897 | PF00069 | 0.336 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.413 |
MOD_SUMO_for_1 | 398 | 401 | PF00179 | 0.575 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.477 |
MOD_SUMO_for_1 | 914 | 917 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 397 | 406 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 426 | 435 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 597 | 607 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 635 | 644 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 871 | 878 | PF00179 | 0.603 |
TRG_AP2beta_CARGO_1 | 875 | 885 | PF09066 | 0.548 |
TRG_DiLeu_BaEn_3 | 430 | 436 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_4 | 498 | 504 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 666 | 671 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 840 | 845 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 811 | 814 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 947 | 950 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 953 | 956 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 630 | 632 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 666 | 669 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 719 | 721 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 841 | 843 | PF00400 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 355 | 360 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M6 | Leptomonas seymouri | 75% | 100% |
A0A0S4J6N5 | Bodo saltans | 51% | 99% |
A0A1X0NYF6 | Trypanosomatidae | 62% | 100% |
A0A1X0P4K5 | Trypanosomatidae | 20% | 100% |
A0A3R7KAV4 | Trypanosoma rangeli | 63% | 100% |
A0A3S7WZJ4 | Leishmania donovani | 78% | 100% |
C9ZKE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AHA1 | Leishmania infantum | 78% | 100% |
E9AXX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q9J7 | Leishmania major | 77% | 100% |
V5AK68 | Trypanosoma cruzi | 61% | 100% |