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:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4H984
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006400 | tRNA modification | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 11 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0042274 | ribosomal small subunit biogenesis | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044085 | cellular component biogenesis | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051391 | tRNA acetylation | 7 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1990884 | RNA acetylation | 6 | 12 |
GO:1904812 | rRNA acetylation involved in maturation of SSU-rRNA | 8 | 1 |
GO:1990882 | rRNA acetylation | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008080 | N-acetyltransferase activity | 6 | 12 |
GO:0016407 | acetyltransferase activity | 5 | 12 |
GO:0016410 | N-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0000049 | tRNA binding | 5 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:1990883 | rRNA cytidine N-acetyltransferase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 908 | 912 | PF00656 | 0.423 |
CLV_NRD_NRD_1 | 1030 | 1032 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.197 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.174 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 872 | 874 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 901 | 903 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.174 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 901 | 903 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.264 |
CLV_PCSK_PC7_1 | 191 | 197 | PF00082 | 0.174 |
CLV_PCSK_SKI1_1 | 1025 | 1029 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 1031 | 1035 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.174 |
CLV_PCSK_SKI1_1 | 901 | 905 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 951 | 955 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.302 |
DEG_APCC_DBOX_1 | 1061 | 1069 | PF00400 | 0.677 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.374 |
DEG_SCF_FBW7_2 | 731 | 737 | PF00400 | 0.471 |
DEG_SPOP_SBC_1 | 581 | 585 | PF00917 | 0.555 |
DOC_CDC14_PxL_1 | 888 | 896 | PF14671 | 0.337 |
DOC_CKS1_1 | 731 | 736 | PF01111 | 0.468 |
DOC_CYCLIN_RxL_1 | 37 | 49 | PF00134 | 0.461 |
DOC_CYCLIN_RxL_1 | 489 | 500 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 948 | 959 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 764 | 770 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 808 | 814 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 1031 | 1039 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 387 | 395 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 50 | 58 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 761 | 768 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 93 | 99 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 161 | 170 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 424 | 433 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 761 | 770 | PF00069 | 0.536 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 764 | 767 | PF13499 | 0.374 |
DOC_PP2B_LxvP_1 | 808 | 811 | PF13499 | 0.318 |
DOC_PP4_FxxP_1 | 1069 | 1072 | PF00568 | 0.694 |
DOC_PP4_FxxP_1 | 904 | 907 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 1035 | 1039 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 991 | 995 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 998 | 1002 | PF00917 | 0.620 |
DOC_USP7_UBL2_3 | 1028 | 1032 | PF12436 | 0.660 |
DOC_USP7_UBL2_3 | 89 | 93 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 27 | 32 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 313 | 321 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 390 | 394 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 538 | 543 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 725 | 735 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 803 | 808 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 875 | 882 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 960 | 968 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 980 | 985 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 1030 | 1047 | PF00022 | 0.613 |
LIG_Actin_WH2_2 | 646 | 663 | PF00022 | 0.374 |
LIG_APCC_ABBA_1 | 383 | 388 | PF00400 | 0.439 |
LIG_APCC_ABBAyCdc20_2 | 382 | 388 | PF00400 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.562 |
LIG_BIR_III_4 | 560 | 564 | PF00653 | 0.450 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 877 | 881 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_2 | 372 | 378 | PF00533 | 0.536 |
LIG_Clathr_ClatBox_1 | 494 | 498 | PF01394 | 0.450 |
LIG_FHA_1 | 1039 | 1045 | PF00498 | 0.548 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.450 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.382 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.358 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.493 |
LIG_FHA_1 | 727 | 733 | PF00498 | 0.461 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.491 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.272 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.387 |
LIG_FHA_1 | 945 | 951 | PF00498 | 0.383 |
LIG_FHA_2 | 1005 | 1011 | PF00498 | 0.625 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.553 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.402 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.461 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.454 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.550 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.458 |
LIG_FHA_2 | 856 | 862 | PF00498 | 0.317 |
LIG_FHA_2 | 865 | 871 | PF00498 | 0.315 |
LIG_FHA_2 | 930 | 936 | PF00498 | 0.387 |
LIG_GBD_Chelix_1 | 819 | 827 | PF00786 | 0.272 |
LIG_LIR_Apic_2 | 1067 | 1072 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 110 | 117 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 364 | 372 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 639 | 650 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 737 | 748 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 737 | 743 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 744 | 748 | PF02991 | 0.450 |
LIG_MAD2 | 649 | 657 | PF02301 | 0.450 |
LIG_NRBOX | 490 | 496 | PF00104 | 0.450 |
LIG_NRBOX | 803 | 809 | PF00104 | 0.332 |
LIG_PCNA_PIPBox_1 | 173 | 182 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 794 | 808 | PF02747 | 0.332 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.450 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.555 |
LIG_Pex14_2 | 899 | 903 | PF04695 | 0.235 |
LIG_REV1ctd_RIR_1 | 901 | 906 | PF16727 | 0.235 |
LIG_RPA_C_Fungi | 453 | 465 | PF08784 | 0.449 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.302 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.427 |
LIG_SH2_GRB2like | 331 | 334 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 519 | 522 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 740 | 744 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 765 | 768 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 548 | 551 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 769 | 772 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 765 | 768 | PF00017 | 0.119 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 898 | 901 | PF00017 | 0.316 |
LIG_SH3_1 | 480 | 486 | PF00018 | 0.302 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.302 |
LIG_SH3_3 | 733 | 739 | PF00018 | 0.328 |
LIG_SUMO_SIM_anti_2 | 288 | 295 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 43 | 49 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 430 | 437 | PF11976 | 0.423 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.302 |
LIG_TRAF2_1 | 932 | 935 | PF00917 | 0.379 |
LIG_TRFH_1 | 791 | 795 | PF08558 | 0.552 |
LIG_TYR_ITIM | 743 | 748 | PF00017 | 0.265 |
LIG_UBA3_1 | 73 | 79 | PF00899 | 0.238 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.302 |
MOD_CK1_1 | 1038 | 1044 | PF00069 | 0.657 |
MOD_CK1_1 | 1049 | 1055 | PF00069 | 0.686 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.332 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.528 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.305 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.431 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.406 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.353 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.435 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.390 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.335 |
MOD_CK1_1 | 836 | 842 | PF00069 | 0.390 |
MOD_CK1_1 | 943 | 949 | PF00069 | 0.416 |
MOD_CK1_1 | 959 | 965 | PF00069 | 0.360 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.377 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.302 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.295 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.302 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.447 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.442 |
MOD_CK2_1 | 929 | 935 | PF00069 | 0.387 |
MOD_CK2_1 | 980 | 986 | PF00069 | 0.601 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.387 |
MOD_Cter_Amidation | 899 | 902 | PF01082 | 0.333 |
MOD_GlcNHglycan | 1051 | 1054 | PF01048 | 0.670 |
MOD_GlcNHglycan | 1055 | 1058 | PF01048 | 0.645 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.533 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.318 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.423 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.293 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.327 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.389 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.357 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.398 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.250 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.359 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.231 |
MOD_GlcNHglycan | 714 | 718 | PF01048 | 0.392 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.442 |
MOD_GlcNHglycan | 858 | 861 | PF01048 | 0.436 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.506 |
MOD_GlcNHglycan | 942 | 945 | PF01048 | 0.315 |
MOD_GlcNHglycan | 993 | 996 | PF01048 | 0.717 |
MOD_GSK3_1 | 1000 | 1007 | PF00069 | 0.415 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.293 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.661 |
MOD_GSK3_1 | 1045 | 1052 | PF00069 | 0.676 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.302 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.386 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.525 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.386 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.394 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.318 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.516 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.389 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.391 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.291 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.396 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.344 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.360 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.201 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.302 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.345 |
MOD_GSK3_1 | 940 | 947 | PF00069 | 0.420 |
MOD_GSK3_1 | 959 | 966 | PF00069 | 0.420 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.663 |
MOD_LATS_1 | 187 | 193 | PF00433 | 0.302 |
MOD_LATS_1 | 469 | 475 | PF00433 | 0.449 |
MOD_N-GLC_1 | 1053 | 1058 | PF02516 | 0.754 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.660 |
MOD_NEK2_1 | 1044 | 1049 | PF00069 | 0.736 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.302 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.302 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.302 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.372 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.387 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.302 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.306 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.449 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.332 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.311 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.302 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.302 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.302 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.318 |
MOD_PIKK_1 | 944 | 950 | PF00454 | 0.423 |
MOD_PIKK_1 | 989 | 995 | PF00454 | 0.720 |
MOD_PK_1 | 980 | 986 | PF00069 | 0.461 |
MOD_PKA_1 | 1074 | 1080 | PF00069 | 0.743 |
MOD_PKA_1 | 457 | 463 | PF00069 | 0.359 |
MOD_PKA_2 | 1044 | 1050 | PF00069 | 0.635 |
MOD_PKA_2 | 1061 | 1067 | PF00069 | 0.657 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.529 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.465 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.302 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.389 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.343 |
MOD_PKA_2 | 959 | 965 | PF00069 | 0.423 |
MOD_PKA_2 | 984 | 990 | PF00069 | 0.482 |
MOD_PKB_1 | 189 | 197 | PF00069 | 0.417 |
MOD_PKB_1 | 311 | 319 | PF00069 | 0.302 |
MOD_PKB_1 | 873 | 881 | PF00069 | 0.423 |
MOD_Plk_1 | 1039 | 1045 | PF00069 | 0.579 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.400 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.337 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.483 |
MOD_Plk_1 | 779 | 785 | PF00069 | 0.302 |
MOD_Plk_4 | 1039 | 1045 | PF00069 | 0.478 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.302 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.697 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.364 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.365 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.377 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.627 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.302 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.329 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.217 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.316 |
MOD_Plk_4 | 819 | 825 | PF00069 | 0.315 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.191 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.302 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.541 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.343 |
MOD_SUMO_for_1 | 972 | 975 | PF00179 | 0.197 |
MOD_SUMO_rev_2 | 681 | 690 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 981 | 990 | PF00179 | 0.472 |
TRG_AP2beta_CARGO_1 | 639 | 649 | PF09066 | 0.302 |
TRG_DiLeu_BaLyEn_6 | 800 | 805 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 765 | 768 | PF00928 | 0.235 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 871 | 873 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.329 |
TRG_NES_CRM1_1 | 741 | 755 | PF08389 | 0.423 |
TRG_NLS_MonoExtN_4 | 1028 | 1035 | PF00514 | 0.672 |
TRG_NLS_MonoExtN_4 | 1071 | 1077 | PF00514 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 468 | 472 | PF00026 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 794 | 799 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 813 | 818 | PF00026 | 0.140 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8D1 | Leptomonas seymouri | 80% | 100% |
A0A0S4J7H9 | Bodo saltans | 59% | 100% |
A0A1X0NTC6 | Trypanosomatidae | 64% | 100% |
A0A3Q8IAZ3 | Leishmania donovani | 89% | 100% |
A0A422NAR4 | Trypanosoma rangeli | 64% | 100% |
A1RY08 | Thermofilum pendens (strain DSM 2475 / Hrk 5) | 26% | 100% |
A4HXK2 | Leishmania infantum | 89% | 100% |
C9ZP92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E9AR97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O01757 | Caenorhabditis elegans | 41% | 100% |
P53914 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 41% | 100% |
P87115 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
Q4QE66 | Leishmania major | 88% | 100% |
Q55EJ3 | Dictyostelium discoideum | 40% | 100% |
Q8K224 | Mus musculus | 41% | 100% |
Q9H0A0 | Homo sapiens | 43% | 100% |
Q9M2Q4 | Arabidopsis thaliana | 40% | 100% |
Q9W3C1 | Drosophila melanogaster | 40% | 100% |
Q9XIK4 | Arabidopsis thaliana | 40% | 100% |
V5BJF5 | Trypanosoma cruzi | 63% | 100% |