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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HC16
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008213 | protein alkylation | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0018193 | peptidyl-amino acid modification | 5 | 7 |
GO:0018195 | peptidyl-arginine modification | 6 | 7 |
GO:0018216 | peptidyl-arginine methylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0032259 | methylation | 2 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0043414 | macromolecule methylation | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019918 | peptidyl-arginine methylation, to symmetrical-dimethyl arginine | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034969 | histone arginine methylation | 6 | 1 |
GO:0035246 | peptidyl-arginine N-methylation | 6 | 1 |
GO:0035247 | peptidyl-arginine omega-N-methylation | 7 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0008168 | methyltransferase activity | 4 | 7 |
GO:0008170 | N-methyltransferase activity | 5 | 7 |
GO:0008276 | protein methyltransferase activity | 3 | 7 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 7 |
GO:0016273 | arginine N-methyltransferase activity | 6 | 7 |
GO:0016274 | protein-arginine N-methyltransferase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0008469 | histone arginine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 746 | 750 | PF00656 | 0.491 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 962 | 964 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 968 | 970 | PF00675 | 0.272 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 962 | 964 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 633 | 635 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 859 | 861 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 808 | 812 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.268 |
CLV_Separin_Metazoa | 525 | 529 | PF03568 | 0.370 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.426 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.573 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.436 |
DOC_CKS1_1 | 422 | 427 | PF01111 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 569 | 575 | PF00134 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 727 | 733 | PF00134 | 0.512 |
DOC_MAPK_gen_1 | 170 | 179 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 528 | 534 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 866 | 873 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 951 | 960 | PF00069 | 0.468 |
DOC_MAPK_RevD_3 | 515 | 530 | PF00069 | 0.449 |
DOC_MAPK_RevD_3 | 956 | 970 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 769 | 776 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.468 |
DOC_PP2B_LxvP_1 | 727 | 730 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 810 | 813 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 839 | 842 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 881 | 884 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 989 | 993 | PF00917 | 0.523 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 911 | 916 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 985 | 990 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 327 | 337 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 390 | 396 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 492 | 496 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 808 | 813 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 835 | 840 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 851 | 857 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 875 | 880 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 962 | 967 | PF00244 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.523 |
LIG_BIR_III_2 | 316 | 320 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 622 | 626 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 794 | 798 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 877 | 881 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_2 | 622 | 628 | PF00533 | 0.407 |
LIG_CaM_IQ_9 | 955 | 971 | PF13499 | 0.512 |
LIG_deltaCOP1_diTrp_1 | 694 | 704 | PF00928 | 0.512 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.480 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.423 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.371 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.522 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.492 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.501 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.395 |
LIG_FHA_1 | 785 | 791 | PF00498 | 0.468 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.512 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.557 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.670 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.482 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.575 |
LIG_FHA_2 | 976 | 982 | PF00498 | 0.526 |
LIG_GBD_Chelix_1 | 739 | 747 | PF00786 | 0.312 |
LIG_IBAR_NPY_1 | 776 | 778 | PF08397 | 0.289 |
LIG_LIR_Apic_2 | 494 | 498 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 787 | 792 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 878 | 884 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 103 | 113 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 141 | 148 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 541 | 551 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 560 | 569 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 582 | 592 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 685 | 692 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 694 | 704 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 920 | 931 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 538 | 543 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 560 | 565 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 694 | 700 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 920 | 926 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 976 | 982 | PF02991 | 0.407 |
LIG_MLH1_MIPbox_1 | 622 | 626 | PF16413 | 0.407 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.413 |
LIG_OCRL_FandH_1 | 624 | 636 | PF00620 | 0.512 |
LIG_PCNA_PIPBox_1 | 542 | 551 | PF02747 | 0.402 |
LIG_PCNA_yPIPBox_3 | 170 | 183 | PF02747 | 0.392 |
LIG_PCNA_yPIPBox_3 | 537 | 549 | PF02747 | 0.468 |
LIG_Pex14_1 | 509 | 513 | PF04695 | 0.371 |
LIG_Pex14_1 | 975 | 979 | PF04695 | 0.468 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.469 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.430 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.416 |
LIG_Pex14_2 | 848 | 852 | PF04695 | 0.468 |
LIG_Pex14_2 | 926 | 930 | PF04695 | 0.468 |
LIG_PTB_Apo_2 | 407 | 414 | PF02174 | 0.532 |
LIG_PTB_Phospho_1 | 407 | 413 | PF10480 | 0.532 |
LIG_REV1ctd_RIR_1 | 623 | 632 | PF16727 | 0.512 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.574 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.633 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.568 |
LIG_SH2_CRK | 543 | 547 | PF00017 | 0.321 |
LIG_SH2_GRB2like | 408 | 411 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 446 | 450 | PF00017 | 0.665 |
LIG_SH2_PTP2 | 495 | 498 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 786 | 790 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 973 | 977 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 895 | 898 | PF00017 | 0.468 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.549 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.362 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.532 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.417 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.468 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.468 |
LIG_SH3_3 | 809 | 815 | PF00018 | 0.468 |
LIG_SH3_3 | 838 | 844 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 707 | 712 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 826 | 831 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 86 | 92 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 869 | 874 | PF11976 | 0.455 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.529 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.476 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.444 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.301 |
LIG_TRAF2_1 | 720 | 723 | PF00917 | 0.438 |
LIG_TRFH_1 | 930 | 934 | PF08558 | 0.468 |
LIG_TYR_ITIM | 977 | 982 | PF00017 | 0.464 |
LIG_UBA3_1 | 545 | 552 | PF00899 | 0.397 |
LIG_UBA3_1 | 59 | 64 | PF00899 | 0.536 |
LIG_UBA3_1 | 674 | 679 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 248 | 253 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 562 | 567 | PF05994 | 0.363 |
LIG_WW_3 | 883 | 887 | PF00397 | 0.405 |
MOD_CDK_SPxxK_3 | 320 | 327 | PF00069 | 0.454 |
MOD_CDK_SPxxK_3 | 911 | 918 | PF00069 | 0.407 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.480 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.467 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.546 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.494 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.655 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.521 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.606 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.374 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.537 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.492 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.580 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.555 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.621 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.606 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.468 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.575 |
MOD_CK2_1 | 962 | 968 | PF00069 | 0.445 |
MOD_CMANNOS | 972 | 975 | PF00535 | 0.268 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.473 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.581 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.444 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.374 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.631 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.613 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.369 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.312 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.207 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.314 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.268 |
MOD_GlcNHglycan | 874 | 878 | PF01048 | 0.223 |
MOD_GlcNHglycan | 889 | 892 | PF01048 | 0.318 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.289 |
MOD_GlcNHglycan | 902 | 905 | PF01048 | 0.304 |
MOD_GlcNHglycan | 946 | 949 | PF01048 | 0.210 |
MOD_GlcNHglycan | 989 | 992 | PF01048 | 0.588 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.495 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.563 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.472 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.418 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.403 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.597 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.468 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.482 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.468 |
MOD_GSK3_1 | 902 | 909 | PF00069 | 0.512 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.653 |
MOD_GSK3_1 | 985 | 992 | PF00069 | 0.534 |
MOD_LATS_1 | 388 | 394 | PF00433 | 0.478 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.518 |
MOD_N-GLC_1 | 723 | 728 | PF02516 | 0.263 |
MOD_N-GLC_1 | 831 | 836 | PF02516 | 0.275 |
MOD_N-GLC_2 | 24 | 26 | PF02516 | 0.425 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.434 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.464 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.482 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.482 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.425 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.475 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.449 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.468 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.468 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.468 |
MOD_NEK2_1 | 873 | 878 | PF00069 | 0.427 |
MOD_NEK2_1 | 900 | 905 | PF00069 | 0.512 |
MOD_NEK2_2 | 1007 | 1012 | PF00069 | 0.300 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.497 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.564 |
MOD_PIKK_1 | 574 | 580 | PF00454 | 0.407 |
MOD_PIKK_1 | 695 | 701 | PF00454 | 0.463 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.592 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.398 |
MOD_PKA_1 | 962 | 968 | PF00069 | 0.444 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.523 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.559 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.502 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.551 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.521 |
MOD_PKA_2 | 850 | 856 | PF00069 | 0.420 |
MOD_PKA_2 | 887 | 893 | PF00069 | 0.405 |
MOD_PKA_2 | 962 | 968 | PF00069 | 0.468 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.450 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.596 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.481 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.512 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.463 |
MOD_Plk_1 | 723 | 729 | PF00069 | 0.459 |
MOD_Plk_1 | 973 | 979 | PF00069 | 0.468 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.505 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.668 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.550 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.530 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.425 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.592 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.406 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.583 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.352 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.563 |
MOD_Plk_4 | 875 | 881 | PF00069 | 0.512 |
MOD_Plk_4 | 906 | 912 | PF00069 | 0.551 |
MOD_Plk_4 | 921 | 927 | PF00069 | 0.411 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.424 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.438 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.576 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.501 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.688 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.570 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.468 |
MOD_ProDKin_1 | 911 | 917 | PF00069 | 0.427 |
MOD_ProDKin_1 | 985 | 991 | PF00069 | 0.573 |
MOD_SUMO_rev_2 | 947 | 953 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 965 | 971 | PF00179 | 0.386 |
TRG_DiLeu_BaEn_2 | 177 | 183 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 22 | 28 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 722 | 728 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 653 | 658 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 862 | 865 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 979 | 982 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 885 | 888 | PF00400 | 0.405 |
TRG_NES_CRM1_1 | 699 | 714 | PF08389 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 128 | 132 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT81 | Leptomonas seymouri | 56% | 93% |
A0A3S7WWP9 | Leishmania donovani | 77% | 94% |
A4HZE2 | Leishmania infantum | 77% | 94% |
E9AVC9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QC50 | Leishmania major | 79% | 100% |