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:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1B9
Term | Name | Level | Count |
---|---|---|---|
GO:0000460 | maturation of 5.8S rRNA | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006401 | RNA catabolic process | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 12 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046700 | heterocycle catabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003724 | RNA helicase activity | 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:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
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:0140098 | catalytic activity, acting on RNA | 3 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.247 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 957 | 959 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.297 |
CLV_PCSK_PC1ET2_1 | 746 | 748 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 957 | 959 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 866 | 870 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 899 | 903 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 948 | 952 | PF00082 | 0.258 |
CLV_Separin_Metazoa | 132 | 136 | PF03568 | 0.447 |
CLV_Separin_Metazoa | 143 | 147 | PF03568 | 0.447 |
CLV_Separin_Metazoa | 926 | 930 | PF03568 | 0.491 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.508 |
DOC_ANK_TNKS_1 | 935 | 942 | PF00023 | 0.447 |
DOC_CYCLIN_RxL_1 | 394 | 404 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 446 | 454 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 529 | 537 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 676 | 684 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 304 | 312 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 384 | 391 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 447 | 456 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 162 | 169 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 326 | 332 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 395 | 401 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 412 | 419 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 956 | 963 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 608 | 611 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 847 | 850 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 853 | 856 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 868 | 872 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 939 | 943 | PF00917 | 0.458 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 840 | 845 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 934 | 939 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 507 | 515 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 584 | 591 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 866 | 871 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 929 | 938 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 130 | 148 | PF00022 | 0.447 |
LIG_Actin_WH2_2 | 780 | 797 | PF00022 | 0.368 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.458 |
LIG_Clathr_ClatBox_1 | 493 | 497 | PF01394 | 0.387 |
LIG_deltaCOP1_diTrp_1 | 590 | 599 | PF00928 | 0.508 |
LIG_FAT_LD_1 | 924 | 932 | PF03623 | 0.508 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.453 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.447 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.458 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.511 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.512 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.447 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.541 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.458 |
LIG_FHA_1 | 812 | 818 | PF00498 | 0.447 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.447 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.447 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.646 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.447 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.316 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.533 |
LIG_FHA_2 | 802 | 808 | PF00498 | 0.447 |
LIG_FHA_2 | 909 | 915 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 845 | 850 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 852 | 856 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 229 | 237 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 436 | 444 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 486 | 494 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 508 | 515 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 652 | 661 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 652 | 658 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 740 | 745 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 815 | 821 | PF02991 | 0.447 |
LIG_LYPXL_S_1 | 306 | 310 | PF13949 | 0.331 |
LIG_LYPXL_yS_3 | 307 | 310 | PF13949 | 0.332 |
LIG_NRBOX | 812 | 818 | PF00104 | 0.447 |
LIG_PDZ_Class_2 | 963 | 968 | PF00595 | 0.382 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.447 |
LIG_PTB_Apo_2 | 602 | 609 | PF02174 | 0.552 |
LIG_PTB_Apo_2 | 95 | 102 | PF02174 | 0.447 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.390 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.329 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 181 | 184 | PF00017 | 0.447 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.338 |
LIG_SH2_SRC | 75 | 78 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 895 | 898 | PF00017 | 0.488 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 169 | 177 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 826 | 835 | PF11976 | 0.447 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.497 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.517 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.488 |
LIG_TYR_ITIM | 485 | 490 | PF00017 | 0.335 |
LIG_TYR_ITSM | 210 | 217 | PF00017 | 0.392 |
LIG_UBA3_1 | 231 | 238 | PF00899 | 0.454 |
LIG_UBA3_1 | 294 | 299 | PF00899 | 0.388 |
LIG_UBA3_1 | 379 | 384 | PF00899 | 0.493 |
LIG_UBA3_1 | 812 | 819 | PF00899 | 0.447 |
LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.419 |
LIG_WRC_WIRS_1 | 480 | 485 | PF05994 | 0.477 |
MOD_CDC14_SPxK_1 | 91 | 94 | PF00782 | 0.447 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.447 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.574 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.447 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.518 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.466 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.458 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.383 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.479 |
MOD_CK1_1 | 824 | 830 | PF00069 | 0.472 |
MOD_CK1_1 | 871 | 877 | PF00069 | 0.447 |
MOD_CK1_1 | 908 | 914 | PF00069 | 0.552 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.710 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.552 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.529 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.447 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.556 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.506 |
MOD_CK2_1 | 802 | 808 | PF00069 | 0.447 |
MOD_CK2_1 | 878 | 884 | PF00069 | 0.463 |
MOD_CK2_1 | 886 | 892 | PF00069 | 0.426 |
MOD_CK2_1 | 908 | 914 | PF00069 | 0.508 |
MOD_Cter_Amidation | 444 | 447 | PF01082 | 0.237 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.247 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.247 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.247 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.341 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.249 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.297 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.245 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.325 |
MOD_GlcNHglycan | 870 | 873 | PF01048 | 0.255 |
MOD_GlcNHglycan | 932 | 935 | PF01048 | 0.333 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.447 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.485 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.640 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.447 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.480 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.447 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.348 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.405 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.479 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.440 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.488 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.392 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.474 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.496 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.479 |
MOD_GSK3_1 | 930 | 937 | PF00069 | 0.533 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.702 |
MOD_N-GLC_1 | 606 | 611 | PF02516 | 0.297 |
MOD_N-GLC_1 | 879 | 884 | PF02516 | 0.303 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.539 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.447 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.443 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.497 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.355 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.447 |
MOD_NEK2_1 | 891 | 896 | PF00069 | 0.428 |
MOD_NEK2_1 | 962 | 967 | PF00069 | 0.499 |
MOD_NEK2_2 | 116 | 121 | PF00069 | 0.447 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.331 |
MOD_NEK2_2 | 660 | 665 | PF00069 | 0.469 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.528 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.526 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.548 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.495 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.447 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.753 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.447 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.560 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.469 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.447 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.447 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.543 |
MOD_Plk_1 | 878 | 884 | PF00069 | 0.436 |
MOD_Plk_1 | 891 | 897 | PF00069 | 0.385 |
MOD_Plk_2-3 | 879 | 885 | PF00069 | 0.472 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.552 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.447 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.545 |
MOD_Plk_4 | 886 | 892 | PF00069 | 0.447 |
MOD_Plk_4 | 962 | 968 | PF00069 | 0.504 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.547 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.533 |
MOD_ProDKin_1 | 840 | 846 | PF00069 | 0.447 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.447 |
MOD_ProDKin_1 | 934 | 940 | PF00069 | 0.447 |
MOD_SUMO_for_1 | 315 | 318 | PF00179 | 0.408 |
MOD_SUMO_for_1 | 758 | 761 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 349 | 359 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 517 | 526 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 771 | 777 | PF00179 | 0.414 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 296 | 301 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 335 | 340 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_1 | 808 | 813 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_3 | 772 | 778 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_4 | 353 | 359 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 781 | 783 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 921 | 923 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 292 | 303 | PF08389 | 0.403 |
TRG_NLS_Bipartite_1 | 782 | 799 | PF00514 | 0.374 |
TRG_NLS_MonoExtC_3 | 25 | 30 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 23 | 30 | PF00514 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.269 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 858 | 862 | PF00026 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 922 | 926 | PF00026 | 0.247 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDH1 | Leptomonas seymouri | 89% | 100% |
A0A0S4JCF9 | Bodo saltans | 70% | 100% |
A0A1X0NKW0 | Trypanosomatidae | 77% | 100% |
A0A3R7NR74 | Trypanosoma rangeli | 76% | 100% |
A0A3S7XB63 | Leishmania donovani | 97% | 100% |
A4HPG6 | Leishmania braziliensis | 92% | 100% |
A4ID88 | Leishmania infantum | 97% | 100% |
D0A3H7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 74% | 100% |
E9AT78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
F4JAA5 | Arabidopsis thaliana | 35% | 72% |
O13799 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 94% |
O14232 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 87% |
O59801 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 80% |
P35207 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 75% |
P42285 | Homo sapiens | 47% | 93% |
P47047 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 46% | 90% |
Q15477 | Homo sapiens | 36% | 78% |
Q23223 | Caenorhabditis elegans | 44% | 94% |
Q9CZU3 | Mus musculus | 47% | 93% |
Q9XIF2 | Arabidopsis thaliana | 42% | 98% |
Q9ZBD8 | Mycobacterium leprae (strain TN) | 29% | 100% |
Q9ZVW2 | Arabidopsis thaliana | 42% | 97% |
V5BPT8 | Trypanosoma cruzi | 75% | 100% |