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: Q4Q648
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:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
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:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
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:0016310 | phosphorylation | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
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:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
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:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016791 | phosphatase activity | 5 | 2 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 2 |
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:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0046403 | polynucleotide 3'-phosphatase activity | 6 | 2 |
GO:0046404 | polydeoxyribonucleotide 5'-hydroxyl-kinase activity | 7 | 2 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 2 |
GO:0051733 | polydeoxyribonucleotide kinase activity | 6 | 2 |
GO:0051734 | polynucleotide kinase activity | 6 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.379 |
CLV_C14_Caspase3-7 | 547 | 551 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 867 | 869 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 886 | 888 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 910 | 912 | PF00675 | 0.549 |
CLV_PCSK_FUR_1 | 14 | 18 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 867 | 869 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 910 | 912 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 910 | 912 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 426 | 432 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 911 | 915 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 527 | 535 | PF00400 | 0.560 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.763 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.661 |
DOC_ANK_TNKS_1 | 215 | 222 | PF00023 | 0.452 |
DOC_CKS1_1 | 720 | 725 | PF01111 | 0.359 |
DOC_CYCLIN_RxL_1 | 799 | 810 | PF00134 | 0.487 |
DOC_CYCLIN_yClb1_LxF_4 | 331 | 337 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 806 | 809 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 85 | 91 | PF00134 | 0.566 |
DOC_MAPK_gen_1 | 77 | 85 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 910 | 916 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 724 | 733 | PF00069 | 0.479 |
DOC_PP2B_LxvP_1 | 389 | 392 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 806 | 809 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 914 | 917 | PF13499 | 0.451 |
DOC_PP2B_PxIxI_1 | 879 | 885 | PF00149 | 0.321 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.504 |
DOC_PP4_FxxP_1 | 581 | 584 | PF00568 | 0.450 |
DOC_PP4_FxxP_1 | 720 | 723 | PF00568 | 0.345 |
DOC_SPAK_OSR1_1 | 216 | 220 | PF12202 | 0.357 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.465 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 734 | 739 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 897 | 902 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 247 | 254 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.812 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 626 | 635 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 708 | 713 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 759 | 766 | PF00244 | 0.349 |
LIG_Actin_WH2_2 | 541 | 558 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 743 | 761 | PF00022 | 0.326 |
LIG_APCC_ABBA_1 | 316 | 321 | PF00400 | 0.402 |
LIG_BIR_III_4 | 443 | 447 | PF00653 | 0.507 |
LIG_BIR_III_4 | 557 | 561 | PF00653 | 0.459 |
LIG_BIR_III_4 | 858 | 862 | PF00653 | 0.333 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.497 |
LIG_Clathr_ClatBox_1 | 730 | 734 | PF01394 | 0.309 |
LIG_CtBP_PxDLS_1 | 657 | 661 | PF00389 | 0.468 |
LIG_CtBP_PxDLS_1 | 808 | 812 | PF00389 | 0.324 |
LIG_deltaCOP1_diTrp_1 | 500 | 508 | PF00928 | 0.392 |
LIG_deltaCOP1_diTrp_1 | 537 | 545 | PF00928 | 0.505 |
LIG_EH1_1 | 739 | 747 | PF00400 | 0.365 |
LIG_EVH1_1 | 783 | 787 | PF00568 | 0.351 |
LIG_EVH1_1 | 914 | 918 | PF00568 | 0.347 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.587 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.547 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.464 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.504 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.403 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.428 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.335 |
LIG_FHA_1 | 847 | 853 | PF00498 | 0.470 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.670 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.500 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.552 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.501 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.517 |
LIG_FHA_2 | 760 | 766 | PF00498 | 0.499 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 185 | 190 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 408 | 413 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 661 | 667 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 719 | 723 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 312 | 319 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 652 | 660 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 788 | 795 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 788 | 792 | PF02991 | 0.477 |
LIG_NRBOX | 595 | 601 | PF00104 | 0.365 |
LIG_NRBOX | 839 | 845 | PF00104 | 0.479 |
LIG_PCNA_yPIPBox_3 | 797 | 805 | PF02747 | 0.424 |
LIG_PCNA_yPIPBox_3 | 912 | 926 | PF02747 | 0.317 |
LIG_Pex14_1 | 311 | 315 | PF04695 | 0.425 |
LIG_Pex14_1 | 508 | 512 | PF04695 | 0.446 |
LIG_Pex14_2 | 315 | 319 | PF04695 | 0.441 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.589 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.481 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.453 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.531 |
LIG_SH2_CRK | 789 | 793 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 653 | 656 | PF00017 | 0.536 |
LIG_SH2_GRB2like | 894 | 897 | PF00017 | 0.296 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 789 | 793 | PF00017 | 0.384 |
LIG_SH2_PTP2 | 597 | 600 | PF00017 | 0.372 |
LIG_SH2_SRC | 131 | 134 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 674 | 678 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 776 | 780 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 894 | 898 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 383 | 386 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.477 |
LIG_SH3_1 | 912 | 918 | PF00018 | 0.350 |
LIG_SH3_2 | 905 | 910 | PF14604 | 0.545 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.504 |
LIG_SH3_3 | 720 | 726 | PF00018 | 0.537 |
LIG_SH3_3 | 781 | 787 | PF00018 | 0.539 |
LIG_SH3_3 | 902 | 908 | PF00018 | 0.513 |
LIG_SH3_3 | 912 | 918 | PF00018 | 0.407 |
LIG_SUMO_SIM_anti_2 | 575 | 580 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 656 | 661 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 728 | 734 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 847 | 854 | PF11976 | 0.425 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.501 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.560 |
LIG_TRAF2_1 | 698 | 701 | PF00917 | 0.610 |
LIG_UBA3_1 | 531 | 536 | PF00899 | 0.442 |
LIG_UBA3_1 | 639 | 648 | PF00899 | 0.427 |
LIG_WW_1 | 786 | 789 | PF00397 | 0.332 |
LIG_WW_1 | 891 | 894 | PF00397 | 0.411 |
MOD_CDK_SPK_2 | 719 | 724 | PF00069 | 0.437 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.425 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.622 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.558 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.742 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.468 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.572 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.544 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.327 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.491 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.527 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.519 |
MOD_Cter_Amidation | 615 | 618 | PF01082 | 0.546 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.522 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.450 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.583 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.561 |
MOD_GlcNHglycan | 327 | 331 | PF01048 | 0.557 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.425 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.429 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.584 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.332 |
MOD_GlcNHglycan | 613 | 617 | PF01048 | 0.421 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.689 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.720 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.600 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.532 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.545 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.655 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.767 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.637 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.739 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.429 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.485 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.310 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.536 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.484 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.440 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.324 |
MOD_N-GLC_1 | 137 | 142 | PF02516 | 0.569 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.670 |
MOD_N-GLC_1 | 695 | 700 | PF02516 | 0.512 |
MOD_N-GLC_1 | 752 | 757 | PF02516 | 0.523 |
MOD_N-GLC_1 | 918 | 923 | PF02516 | 0.481 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.759 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.392 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.360 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.274 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.460 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.448 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.421 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.496 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.491 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.460 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.539 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.483 |
MOD_NEK2_1 | 821 | 826 | PF00069 | 0.357 |
MOD_NEK2_1 | 844 | 849 | PF00069 | 0.496 |
MOD_NEK2_2 | 687 | 692 | PF00069 | 0.505 |
MOD_NEK2_2 | 754 | 759 | PF00069 | 0.357 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.635 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.430 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.442 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.378 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.731 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.335 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.494 |
MOD_PIKK_1 | 822 | 828 | PF00454 | 0.298 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.671 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.815 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.604 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.405 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.551 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.446 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.571 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.387 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.506 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.545 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.423 |
MOD_Plk_1 | 918 | 924 | PF00069 | 0.490 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.486 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.433 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.366 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.326 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.419 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.363 |
MOD_Plk_4 | 918 | 924 | PF00069 | 0.417 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.578 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.533 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.462 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.753 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.536 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.544 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.518 |
MOD_ProDKin_1 | 734 | 740 | PF00069 | 0.529 |
MOD_ProDKin_1 | 897 | 903 | PF00069 | 0.393 |
MOD_SUMO_rev_2 | 550 | 555 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 641 | 649 | PF00179 | 0.439 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.333 |
TRG_DiLeu_LyEn_5 | 78 | 83 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 789 | 792 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 866 | 868 | PF00400 | 0.337 |
TRG_NES_CRM1_1 | 734 | 748 | PF08389 | 0.406 |
TRG_NLS_MonoExtN_4 | 908 | 914 | PF00514 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 697 | 701 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6S2 | Leptomonas seymouri | 59% | 100% |
A0A0S4J4W5 | Bodo saltans | 35% | 100% |
A0A1X0NHZ8 | Trypanosomatidae | 33% | 100% |
A0A3R7M5Z2 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X4Q3 | Leishmania donovani | 89% | 100% |
A4HJJ5 | Leishmania braziliensis | 70% | 100% |
A4I6Z2 | Leishmania infantum | 89% | 100% |
E9B213 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |