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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005829 | cytosol | 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: Q4QC50
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
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:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 7 |
GO:0018195 | peptidyl-arginine modification | 6 | 7 |
GO:0018216 | peptidyl-arginine methylation | 5 | 7 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019918 | peptidyl-arginine methylation, to symmetrical-dimethyl arginine | 8 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0032259 | methylation | 2 | 7 |
GO:0034969 | histone arginine methylation | 6 | 2 |
GO:0035246 | peptidyl-arginine N-methylation | 6 | 2 |
GO:0035247 | peptidyl-arginine omega-N-methylation | 7 | 2 |
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:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
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:0008469 | histone arginine N-methyltransferase activity | 5 | 2 |
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:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1037 | 1041 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 1050 | 1054 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 803 | 807 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 1021 | 1023 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 926 | 928 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 1021 | 1023 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 925 | 927 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 925 | 927 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 921 | 927 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 865 | 869 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 892 | 896 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.747 |
CLV_Separin_Metazoa | 582 | 586 | PF03568 | 0.469 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.542 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.593 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.706 |
DOC_ANK_TNKS_1 | 440 | 447 | PF00023 | 0.723 |
DOC_CDC14_PxL_1 | 597 | 605 | PF14671 | 0.511 |
DOC_CKS1_1 | 349 | 354 | PF01111 | 0.536 |
DOC_CYCLIN_yCln2_LP_2 | 626 | 632 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 784 | 790 | PF00134 | 0.618 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 585 | 591 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 1011 | 1019 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.464 |
DOC_MAPK_RevD_3 | 572 | 587 | PF00069 | 0.601 |
DOC_PP1_RVXF_1 | 24 | 31 | PF00149 | 0.692 |
DOC_PP1_RVXF_1 | 826 | 833 | PF00149 | 0.584 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 784 | 787 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 867 | 870 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 896 | 899 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 415 | 418 | PF00568 | 0.605 |
DOC_PP4_FxxP_1 | 940 | 943 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 1007 | 1011 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 1048 | 1052 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 520 | 524 | PF12436 | 0.755 |
DOC_WW_Pin1_4 | 1044 | 1049 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.838 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 1021 | 1026 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 547 | 553 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 892 | 897 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 934 | 939 | PF00244 | 0.589 |
LIG_BIR_III_4 | 443 | 447 | PF00653 | 0.817 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.701 |
LIG_BRCT_BRCA1_1 | 404 | 408 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 851 | 855 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 936 | 940 | PF00533 | 0.618 |
LIG_CaM_IQ_9 | 1014 | 1030 | PF13499 | 0.618 |
LIG_CaM_IQ_9 | 298 | 314 | PF13499 | 0.527 |
LIG_CtBP_PxDLS_1 | 167 | 171 | PF00389 | 0.716 |
LIG_deltaCOP1_diTrp_1 | 751 | 761 | PF00928 | 0.618 |
LIG_eIF4E_1 | 24 | 30 | PF01652 | 0.695 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.522 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.681 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.497 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.586 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.632 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.546 |
LIG_FHA_1 | 842 | 848 | PF00498 | 0.526 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.618 |
LIG_FHA_1 | 970 | 976 | PF00498 | 0.534 |
LIG_FHA_2 | 1021 | 1027 | PF00498 | 0.506 |
LIG_FHA_2 | 1035 | 1041 | PF00498 | 0.590 |
LIG_FHA_2 | 1048 | 1054 | PF00498 | 0.572 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.725 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.706 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.725 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.647 |
LIG_FHA_2 | 775 | 781 | PF00498 | 0.618 |
LIG_GBD_Chelix_1 | 796 | 804 | PF00786 | 0.346 |
LIG_LIR_Apic_2 | 551 | 555 | PF02991 | 0.713 |
LIG_LIR_Apic_2 | 844 | 849 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 937 | 943 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 188 | 195 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 493 | 500 | PF02991 | 0.771 |
LIG_LIR_Gen_1 | 548 | 558 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 639 | 649 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 657 | 668 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 751 | 761 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 979 | 990 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.771 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 548 | 553 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 569 | 573 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 617 | 622 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 657 | 663 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 751 | 757 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 979 | 985 | PF02991 | 0.614 |
LIG_LYPXL_yS_3 | 600 | 603 | PF13949 | 0.515 |
LIG_NRBOX | 24 | 30 | PF00104 | 0.695 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.499 |
LIG_OCRL_FandH_1 | 681 | 693 | PF00620 | 0.618 |
LIG_PCNA_PIPBox_1 | 599 | 608 | PF02747 | 0.521 |
LIG_PCNA_yPIPBox_3 | 217 | 230 | PF02747 | 0.486 |
LIG_PCNA_yPIPBox_3 | 594 | 606 | PF02747 | 0.631 |
LIG_PCNA_yPIPBox_3 | 65 | 78 | PF02747 | 0.507 |
LIG_Pex14_1 | 1034 | 1038 | PF04695 | 0.546 |
LIG_Pex14_1 | 566 | 570 | PF04695 | 0.488 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.524 |
LIG_Pex14_2 | 592 | 596 | PF04695 | 0.552 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.626 |
LIG_Pex14_2 | 905 | 909 | PF04695 | 0.546 |
LIG_Pex14_2 | 985 | 989 | PF04695 | 0.546 |
LIG_REV1ctd_RIR_1 | 680 | 689 | PF16727 | 0.618 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.723 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.550 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.712 |
LIG_SH2_CRK | 550 | 554 | PF00017 | 0.729 |
LIG_SH2_NCK_1 | 500 | 504 | PF00017 | 0.787 |
LIG_SH2_NCK_1 | 534 | 538 | PF00017 | 0.705 |
LIG_SH2_PTP2 | 552 | 555 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 1032 | 1036 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.718 |
LIG_SH2_STAP1 | 550 | 554 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 843 | 847 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 322 | 325 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 759 | 762 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 843 | 846 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 954 | 957 | PF00017 | 0.546 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.661 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.414 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.681 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.570 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.710 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.520 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.546 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.546 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.735 |
LIG_SH3_3 | 866 | 872 | PF00018 | 0.546 |
LIG_SH3_3 | 895 | 901 | PF00018 | 0.618 |
LIG_SUMO_SIM_anti_2 | 764 | 769 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 883 | 888 | PF11976 | 0.618 |
LIG_TRAF2_1 | 1006 | 1009 | PF00917 | 0.537 |
LIG_TRAF2_1 | 1024 | 1027 | PF00917 | 0.571 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.661 |
LIG_TRFH_1 | 989 | 993 | PF08558 | 0.546 |
LIG_UBA3_1 | 602 | 609 | PF00899 | 0.502 |
LIG_UBA3_1 | 731 | 736 | PF00899 | 0.546 |
LIG_UBA3_1 | 94 | 99 | PF00899 | 0.715 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.570 |
LIG_WRC_WIRS_1 | 619 | 624 | PF05994 | 0.512 |
LIG_WW_1 | 479 | 482 | PF00397 | 0.757 |
LIG_WW_3 | 17 | 21 | PF00397 | 0.570 |
MOD_CDK_SPK_2 | 1044 | 1049 | PF00069 | 0.617 |
MOD_CDK_SPK_2 | 371 | 376 | PF00069 | 0.665 |
MOD_CDK_SPxxK_3 | 693 | 700 | PF00069 | 0.574 |
MOD_CK1_1 | 1047 | 1053 | PF00069 | 0.677 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.705 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.691 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.635 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.571 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.554 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.799 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.671 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.540 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.502 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.742 |
MOD_CK2_1 | 1020 | 1026 | PF00069 | 0.516 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.690 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.723 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.704 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.660 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.701 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.546 |
MOD_CK2_1 | 774 | 780 | PF00069 | 0.618 |
MOD_CMANNOS | 1031 | 1034 | PF00535 | 0.346 |
MOD_GlcNHglycan | 1050 | 1053 | PF01048 | 0.739 |
MOD_GlcNHglycan | 1054 | 1057 | PF01048 | 0.728 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.632 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.622 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.625 |
MOD_GlcNHglycan | 469 | 474 | PF01048 | 0.654 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.672 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.686 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.699 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.418 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.333 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.346 |
MOD_GlcNHglycan | 955 | 958 | PF01048 | 0.365 |
MOD_GlcNHglycan | 961 | 964 | PF01048 | 0.376 |
MOD_GSK3_1 | 1044 | 1051 | PF00069 | 0.653 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.744 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.776 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.613 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.521 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.601 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.645 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.424 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.706 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.702 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.546 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.546 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.546 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.618 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.709 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.650 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.353 |
MOD_N-GLC_1 | 881 | 886 | PF02516 | 0.403 |
MOD_N-GLC_1 | 888 | 893 | PF02516 | 0.351 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.622 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.535 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.562 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.480 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.503 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.642 |
MOD_NEK2_1 | 757 | 762 | PF00069 | 0.546 |
MOD_NEK2_1 | 800 | 805 | PF00069 | 0.546 |
MOD_NEK2_1 | 881 | 886 | PF00069 | 0.546 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.642 |
MOD_NEK2_1 | 959 | 964 | PF00069 | 0.618 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.494 |
MOD_NEK2_2 | 492 | 497 | PF00069 | 0.567 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.634 |
MOD_PIKK_1 | 752 | 758 | PF00454 | 0.530 |
MOD_PKA_1 | 1021 | 1027 | PF00069 | 0.518 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.577 |
MOD_PKA_2 | 1020 | 1026 | PF00069 | 0.545 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.628 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.690 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.645 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.636 |
MOD_Plk_1 | 1007 | 1013 | PF00069 | 0.574 |
MOD_Plk_1 | 1032 | 1038 | PF00069 | 0.546 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.584 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.702 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.670 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.475 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.725 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.644 |
MOD_Plk_1 | 752 | 758 | PF00069 | 0.623 |
MOD_Plk_1 | 881 | 887 | PF00069 | 0.534 |
MOD_Plk_2-3 | 501 | 507 | PF00069 | 0.788 |
MOD_Plk_2-3 | 928 | 934 | PF00069 | 0.574 |
MOD_Plk_4 | 1066 | 1072 | PF00069 | 0.459 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.602 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.671 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.569 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.709 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.511 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.675 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.640 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.476 |
MOD_Plk_4 | 881 | 887 | PF00069 | 0.609 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.618 |
MOD_Plk_4 | 965 | 971 | PF00069 | 0.603 |
MOD_Plk_4 | 980 | 986 | PF00069 | 0.463 |
MOD_ProDKin_1 | 1044 | 1050 | PF00069 | 0.633 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.692 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.525 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.720 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.836 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.574 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.688 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.546 |
TRG_DiLeu_BaEn_2 | 224 | 230 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_4 | 57 | 63 | PF01217 | 0.663 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.690 |
TRG_DiLeu_BaLyEn_6 | 598 | 603 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 710 | 715 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.691 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 982 | 985 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 546 | 549 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 584 | 587 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 727 | 730 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.433 |
TRG_NES_CRM1_1 | 756 | 771 | PF08389 | 0.546 |
TRG_NLS_MonoExtN_4 | 647 | 654 | PF00514 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 27 | 32 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.643 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT81 | Leptomonas seymouri | 58% | 98% |
A0A3S7WWP9 | Leishmania donovani | 92% | 99% |
A4HC16 | Leishmania braziliensis | 79% | 100% |
A4HZE2 | Leishmania infantum | 92% | 99% |
E9AVC9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |