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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B213
Term | Name | Level | Count |
---|---|---|---|
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008380 | RNA splicing | 7 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003972 | RNA ligase (ATP) activity | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008452 | RNA ligase activity | 4 | 10 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0046403 | polynucleotide 3'-phosphatase activity | 6 | 1 |
GO:0046404 | polydeoxyribonucleotide 5'-hydroxyl-kinase activity | 7 | 1 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 1 |
GO:0051733 | polydeoxyribonucleotide kinase activity | 6 | 1 |
GO:0051734 | polynucleotide kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 371 | 375 | PF00656 | 0.667 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.345 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 866 | 868 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 909 | 911 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 14 | 18 | PF00082 | 0.820 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 866 | 868 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 909 | 911 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 909 | 911 | PF00082 | 0.551 |
CLV_PCSK_PC7_1 | 17 | 23 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 2 | 8 | PF00082 | 0.523 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 801 | 805 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 910 | 914 | PF00082 | 0.574 |
DEG_APCC_DBOX_1 | 526 | 534 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.347 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.721 |
DEG_SCF_FBW7_1 | 136 | 143 | PF00400 | 0.431 |
DOC_ANK_TNKS_1 | 214 | 221 | PF00023 | 0.413 |
DOC_CKS1_1 | 37 | 42 | PF01111 | 0.530 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.285 |
DOC_CYCLIN_RxL_1 | 533 | 543 | PF00134 | 0.308 |
DOC_CYCLIN_RxL_1 | 798 | 809 | PF00134 | 0.470 |
DOC_CYCLIN_yClb1_LxF_4 | 330 | 336 | PF00134 | 0.457 |
DOC_CYCLIN_yCln2_LP_2 | 805 | 808 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 121 | 131 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 534 | 540 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 688 | 698 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 74 | 83 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 909 | 915 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 691 | 698 | PF00069 | 0.335 |
DOC_PP2B_LxvP_1 | 388 | 391 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 696 | 699 | PF13499 | 0.329 |
DOC_PP2B_LxvP_1 | 805 | 808 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.478 |
DOC_PP2B_LxvP_1 | 913 | 916 | PF13499 | 0.419 |
DOC_PP2B_PxIxI_1 | 878 | 884 | PF00149 | 0.308 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 580 | 583 | PF00568 | 0.468 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.476 |
DOC_SPAK_OSR1_1 | 215 | 219 | PF12202 | 0.338 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 787 | 791 | PF00917 | 0.395 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.426 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.360 |
LIG_14-3-3_CanoR_1 | 180 | 190 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 245 | 253 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.812 |
LIG_14-3-3_CanoR_1 | 408 | 412 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 625 | 634 | PF00244 | 0.566 |
LIG_APCC_ABBA_1 | 315 | 320 | PF00400 | 0.366 |
LIG_BIR_III_4 | 442 | 446 | PF00653 | 0.489 |
LIG_BIR_III_4 | 857 | 861 | PF00653 | 0.320 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.317 |
LIG_CtBP_PxDLS_1 | 725 | 729 | PF00389 | 0.431 |
LIG_deltaCOP1_diTrp_1 | 499 | 507 | PF00928 | 0.377 |
LIG_EH1_1 | 53 | 61 | PF00400 | 0.443 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.591 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.324 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.444 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.542 |
LIG_FHA_1 | 633 | 639 | PF00498 | 0.423 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.317 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.416 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.419 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.324 |
LIG_FHA_1 | 846 | 852 | PF00498 | 0.465 |
LIG_FHA_1 | 860 | 866 | PF00498 | 0.216 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.508 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.669 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.457 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.536 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.517 |
LIG_FHA_2 | 759 | 765 | PF00498 | 0.475 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.438 |
LIG_LIR_Apic_2 | 184 | 189 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 407 | 412 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 660 | 666 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 311 | 318 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 650 | 659 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.370 |
LIG_NRBOX | 594 | 600 | PF00104 | 0.347 |
LIG_NRBOX | 838 | 844 | PF00104 | 0.470 |
LIG_PCNA_yPIPBox_3 | 794 | 803 | PF02747 | 0.391 |
LIG_Pex14_1 | 310 | 314 | PF04695 | 0.414 |
LIG_Pex14_1 | 507 | 511 | PF04695 | 0.429 |
LIG_Pex14_2 | 314 | 318 | PF04695 | 0.426 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.601 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.476 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.482 |
LIG_SH2_CRK | 652 | 656 | PF00017 | 0.515 |
LIG_SH2_CRK | 788 | 792 | PF00017 | 0.341 |
LIG_SH2_GRB2like | 652 | 655 | PF00017 | 0.518 |
LIG_SH2_GRB2like | 893 | 896 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 788 | 792 | PF00017 | 0.365 |
LIG_SH2_PTP2 | 596 | 599 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 673 | 677 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 775 | 779 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 788 | 792 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 893 | 897 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 826 | 829 | PF00017 | 0.480 |
LIG_SH3_2 | 904 | 909 | PF14604 | 0.512 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.506 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.584 |
LIG_SH3_3 | 719 | 725 | PF00018 | 0.567 |
LIG_SH3_3 | 780 | 786 | PF00018 | 0.539 |
LIG_SH3_3 | 901 | 907 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 574 | 579 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 655 | 660 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 693 | 700 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 727 | 733 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 846 | 853 | PF11976 | 0.416 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.534 |
LIG_TRFH_1 | 186 | 190 | PF08558 | 0.320 |
LIG_UBA3_1 | 530 | 536 | PF00899 | 0.401 |
LIG_UBA3_1 | 638 | 647 | PF00899 | 0.397 |
LIG_WRC_WIRS_1 | 775 | 780 | PF05994 | 0.403 |
LIG_WW_1 | 890 | 893 | PF00397 | 0.400 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.650 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.595 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.770 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.496 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.579 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.357 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.504 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.458 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.525 |
MOD_CK2_1 | 881 | 887 | PF00069 | 0.179 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.785 |
MOD_Cter_Amidation | 243 | 246 | PF01082 | 0.332 |
MOD_Cter_Amidation | 614 | 617 | PF01082 | 0.535 |
MOD_DYRK1A_RPxSP_1 | 36 | 40 | PF00069 | 0.535 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.487 |
MOD_GlcNHglycan | 174 | 179 | PF01048 | 0.480 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.438 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.568 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.596 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.580 |
MOD_GlcNHglycan | 326 | 330 | PF01048 | 0.509 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.632 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.409 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.607 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.319 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.665 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.507 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.506 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.684 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.658 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.623 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.784 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.338 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.740 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.399 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.516 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.497 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.414 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.527 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.501 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.434 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.312 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.543 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.522 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.585 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.648 |
MOD_N-GLC_1 | 751 | 756 | PF02516 | 0.507 |
MOD_N-GLC_1 | 917 | 922 | PF02516 | 0.442 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.750 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.375 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.323 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.311 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.395 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.439 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.400 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.505 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.512 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.560 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.451 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.386 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.477 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.348 |
MOD_NEK2_1 | 843 | 848 | PF00069 | 0.404 |
MOD_NEK2_2 | 686 | 691 | PF00069 | 0.468 |
MOD_OFUCOSY | 306 | 313 | PF10250 | 0.223 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.343 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.614 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.383 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.401 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.689 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.315 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.262 |
MOD_PIKK_1 | 625 | 631 | PF00454 | 0.463 |
MOD_PKA_1 | 21 | 27 | PF00069 | 0.661 |
MOD_PKA_1 | 245 | 251 | PF00069 | 0.302 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.706 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.814 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.704 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.410 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.548 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.432 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.377 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.443 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.366 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.552 |
MOD_Plk_1 | 917 | 923 | PF00069 | 0.474 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.465 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.418 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.466 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.408 |
MOD_Plk_4 | 774 | 780 | PF00069 | 0.319 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.350 |
MOD_Plk_4 | 917 | 923 | PF00069 | 0.385 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.504 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.459 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.757 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.496 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.690 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.561 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.554 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.526 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.360 |
MOD_SUMO_rev_2 | 549 | 554 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 640 | 648 | PF00179 | 0.409 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 775 | 778 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 788 | 791 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 865 | 867 | PF00400 | 0.312 |
TRG_NES_CRM1_1 | 733 | 747 | PF08389 | 0.397 |
TRG_NLS_MonoExtN_4 | 907 | 913 | PF00514 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 743 | 747 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6S2 | Leptomonas seymouri | 61% | 100% |
A0A0S4J4W5 | Bodo saltans | 35% | 100% |
A0A1X0NHZ8 | Trypanosomatidae | 33% | 100% |
A0A3R7M5Z2 | Trypanosoma rangeli | 37% | 100% |
A0A3S7X4Q3 | Leishmania donovani | 87% | 100% |
A4HJJ5 | Leishmania braziliensis | 73% | 100% |
A4I6Z2 | Leishmania infantum | 87% | 100% |
Q4Q648 | Leishmania major | 88% | 100% |