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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AKG5
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003724 | RNA helicase activity | 3 | 1 |
GO:0003743 | translation initiation factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 656 | 660 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 811 | 815 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 866 | 870 | PF00656 | 0.751 |
CLV_C14_Caspase3-7 | 888 | 892 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 721 | 723 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 877 | 879 | PF00675 | 0.763 |
CLV_NRD_NRD_1 | 918 | 920 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 964 | 966 | PF00675 | 0.610 |
CLV_PCSK_FUR_1 | 874 | 878 | PF00082 | 0.719 |
CLV_PCSK_FUR_1 | 925 | 929 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 877 | 879 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 924 | 926 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 927 | 929 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 964 | 966 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 924 | 926 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 927 | 929 | PF00082 | 0.725 |
CLV_PCSK_PC7_1 | 923 | 929 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 901 | 905 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.497 |
DEG_APCC_DBOX_1 | 428 | 436 | PF00400 | 0.447 |
DEG_APCC_DBOX_1 | 56 | 64 | PF00400 | 0.536 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.740 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 690 | 694 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 862 | 866 | PF00917 | 0.692 |
DOC_CDC14_PxL_1 | 339 | 347 | PF14671 | 0.528 |
DOC_CKS1_1 | 541 | 546 | PF01111 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 610 | 616 | PF00134 | 0.466 |
DOC_MAPK_DCC_7 | 351 | 359 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 206 | 216 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 429 | 437 | PF00069 | 0.154 |
DOC_MAPK_gen_1 | 730 | 737 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 620 | 627 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.572 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.200 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.528 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 920 | 924 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 266 | 275 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 418 | 423 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 429 | 438 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 551 | 555 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 721 | 725 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 925 | 933 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 941 | 947 | PF00244 | 0.358 |
LIG_14-3-3_CterR_2 | 992 | 995 | PF00244 | 0.664 |
LIG_Actin_WH2_2 | 421 | 438 | PF00022 | 0.336 |
LIG_BIR_III_4 | 16 | 20 | PF00653 | 0.462 |
LIG_BIR_III_4 | 902 | 906 | PF00653 | 0.485 |
LIG_CtBP_PxDLS_1 | 261 | 265 | PF00389 | 0.481 |
LIG_EH1_1 | 664 | 672 | PF00400 | 0.531 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.509 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.600 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.432 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.432 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.427 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.440 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.483 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.372 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.370 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.544 |
LIG_FHA_1 | 736 | 742 | PF00498 | 0.443 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.443 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.470 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.415 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.594 |
LIG_FHA_2 | 864 | 870 | PF00498 | 0.740 |
LIG_FHA_2 | 886 | 892 | PF00498 | 0.708 |
LIG_Integrin_RGD_1 | 878 | 880 | PF01839 | 0.650 |
LIG_LIR_Apic_2 | 269 | 275 | PF02991 | 0.403 |
LIG_LIR_Apic_2 | 327 | 333 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 481 | 489 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 553 | 562 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 645 | 655 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 792 | 801 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 967 | 975 | PF02991 | 0.592 |
LIG_LIR_LC3C_4 | 752 | 755 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 553 | 557 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.701 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 663 | 667 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 792 | 796 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 967 | 971 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 987 | 993 | PF02991 | 0.645 |
LIG_NRBOX | 466 | 472 | PF00104 | 0.432 |
LIG_NRBOX | 78 | 84 | PF00104 | 0.560 |
LIG_PDZ_Class_2 | 990 | 995 | PF00595 | 0.661 |
LIG_PTB_Apo_2 | 477 | 484 | PF02174 | 0.478 |
LIG_Rb_LxCxE_1 | 247 | 269 | PF01857 | 0.420 |
LIG_Rb_pABgroove_1 | 842 | 850 | PF01858 | 0.697 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.481 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.448 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.504 |
LIG_SH2_CRK | 968 | 972 | PF00017 | 0.581 |
LIG_SH2_CRK | 990 | 994 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 968 | 972 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 450 | 454 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 58 | 61 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.432 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.606 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.520 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.620 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.468 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.370 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.513 |
LIG_SH3_3 | 791 | 797 | PF00018 | 0.397 |
LIG_SH3_3 | 814 | 820 | PF00018 | 0.653 |
LIG_SH3_3 | 936 | 942 | PF00018 | 0.526 |
LIG_SH3_4 | 920 | 927 | PF00018 | 0.661 |
LIG_SH3_CIN85_PxpxPR_1 | 827 | 832 | PF14604 | 0.671 |
LIG_SUMO_SIM_anti_2 | 215 | 220 | PF11976 | 0.541 |
LIG_SUMO_SIM_anti_2 | 358 | 364 | PF11976 | 0.516 |
LIG_SUMO_SIM_anti_2 | 707 | 715 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 358 | 364 | PF11976 | 0.432 |
LIG_TRAF2_1 | 660 | 663 | PF00917 | 0.510 |
LIG_TRAF2_1 | 808 | 811 | PF00917 | 0.599 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.448 |
LIG_UBA3_1 | 610 | 619 | PF00899 | 0.483 |
LIG_WRC_WIRS_1 | 943 | 948 | PF05994 | 0.500 |
LIG_WW_3 | 920 | 924 | PF00397 | 0.729 |
MOD_CDK_SPxK_1 | 540 | 546 | PF00069 | 0.498 |
MOD_CDK_SPxxK_3 | 73 | 80 | PF00069 | 0.574 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.589 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.685 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.534 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.450 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.678 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.432 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.611 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.673 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.467 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.457 |
MOD_CK1_1 | 929 | 935 | PF00069 | 0.671 |
MOD_CK1_1 | 985 | 991 | PF00069 | 0.620 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.534 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.617 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.457 |
MOD_Cter_Amidation | 584 | 587 | PF01082 | 0.686 |
MOD_Cter_Amidation | 872 | 875 | PF01082 | 0.723 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.721 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.573 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.507 |
MOD_GlcNHglycan | 16 | 20 | PF01048 | 0.590 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.685 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.470 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.494 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.681 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.589 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.251 |
MOD_GlcNHglycan | 409 | 413 | PF01048 | 0.586 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.552 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.693 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.549 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.286 |
MOD_GlcNHglycan | 871 | 874 | PF01048 | 0.703 |
MOD_GlcNHglycan | 928 | 931 | PF01048 | 0.637 |
MOD_GlcNHglycan | 984 | 987 | PF01048 | 0.536 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.682 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.614 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.624 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.576 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.538 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.675 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.583 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.228 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.536 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.589 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.487 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.436 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.518 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.582 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.518 |
MOD_GSK3_1 | 761 | 768 | PF00069 | 0.463 |
MOD_GSK3_1 | 821 | 828 | PF00069 | 0.723 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.757 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.497 |
MOD_LATS_1 | 416 | 422 | PF00433 | 0.601 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.707 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.491 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.497 |
MOD_N-GLC_1 | 869 | 874 | PF02516 | 0.657 |
MOD_N-GLC_1 | 905 | 910 | PF02516 | 0.784 |
MOD_N-GLC_2 | 854 | 856 | PF02516 | 0.615 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.450 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.477 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.626 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.402 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.530 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.479 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.436 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.446 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.692 |
MOD_NEK2_1 | 984 | 989 | PF00069 | 0.536 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.555 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.579 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.212 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.639 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.518 |
MOD_PIKK_1 | 602 | 608 | PF00454 | 0.459 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.443 |
MOD_PIKK_1 | 985 | 991 | PF00454 | 0.600 |
MOD_PK_1 | 418 | 424 | PF00069 | 0.599 |
MOD_PK_1 | 546 | 552 | PF00069 | 0.526 |
MOD_PKA_1 | 587 | 593 | PF00069 | 0.735 |
MOD_PKA_1 | 964 | 970 | PF00069 | 0.625 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.528 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.599 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.215 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.470 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.396 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.446 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.468 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.528 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.624 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.468 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.364 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.506 |
MOD_Plk_2-3 | 676 | 682 | PF00069 | 0.591 |
MOD_Plk_2-3 | 880 | 886 | PF00069 | 0.724 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.708 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.699 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.570 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.378 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.575 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.463 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.494 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.470 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.263 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.702 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.589 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.591 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.549 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.422 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.575 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.515 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.470 |
TRG_DiLeu_BaEn_1 | 720 | 725 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.586 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 606 | 611 | PF01217 | 0.608 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 664 | 667 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 968 | 971 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 990 | 993 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 54 | 57 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 607 | 610 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 730 | 733 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 874 | 877 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 922 | 925 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 963 | 965 | PF00400 | 0.609 |
TRG_NLS_MonoCore_2 | 585 | 590 | PF00514 | 0.570 |
TRG_NLS_MonoExtC_3 | 922 | 927 | PF00514 | 0.729 |
TRG_NLS_MonoExtN_4 | 586 | 591 | PF00514 | 0.571 |
TRG_NLS_MonoExtN_4 | 920 | 927 | PF00514 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 152 | 157 | PF00026 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.257 |
TRG_Pf-PMV_PEXEL_1 | 722 | 727 | PF00026 | 0.275 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0W3 | Leptomonas seymouri | 55% | 100% |
A0A0S4IKX9 | Bodo saltans | 33% | 100% |
A0A1X0NJY6 | Trypanosomatidae | 39% | 100% |
A0A1X0NPK0 | Trypanosomatidae | 23% | 100% |
A0A3S5IQZ7 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WP45 | Leishmania donovani | 88% | 99% |
A4HD50 | Leishmania braziliensis | 77% | 97% |
A4HSI1 | Leishmania infantum | 88% | 99% |
C9ZUC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 98% |
Q2UH00 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 22% | 100% |
Q4QJE3 | Leishmania major | 88% | 100% |