Appears to be a secreted chaperone, related to mammalian HYOU1 proteins. Probably ER-localized as in other eukaryotes
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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 3, no: 7 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005788 | endoplasmic reticulum lumen | 5 | 1 |
GO:0016020 | membrane | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034663 | endoplasmic reticulum chaperone complex | 3 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H4W3
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006986 | response to unfolded protein | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
GO:0030968 | endoplasmic reticulum unfolded protein response | 3 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034620 | cellular response to unfolded protein | 5 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0035966 | response to topologically incorrect protein | 3 | 1 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042026 | protein refolding | 3 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0044183 | protein folding chaperone | 1 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
GO:0051787 | misfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 961 | 965 | PF00656 | 0.673 |
CLV_MEL_PAP_1 | 981 | 987 | PF00089 | 0.566 |
CLV_NRD_NRD_1 | 1013 | 1015 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 1027 | 1029 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 1065 | 1067 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 821 | 823 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 845 | 847 | PF00675 | 0.659 |
CLV_PCSK_FUR_1 | 1025 | 1029 | PF00082 | 0.558 |
CLV_PCSK_FUR_1 | 843 | 847 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 1013 | 1015 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 1027 | 1029 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 1065 | 1067 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 845 | 847 | PF00082 | 0.664 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 515 | 521 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 532 | 538 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 1102 | 1106 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 752 | 760 | PF00400 | 0.515 |
DEG_APCC_KENBOX_2 | 1042 | 1046 | PF00400 | 0.341 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.689 |
DOC_ANK_TNKS_1 | 641 | 648 | PF00023 | 0.321 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.420 |
DOC_MAPK_DCC_7 | 150 | 158 | PF00069 | 0.666 |
DOC_MAPK_DCC_7 | 753 | 761 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 150 | 158 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 447 | 456 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 753 | 761 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 843 | 851 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 150 | 158 | PF00069 | 0.666 |
DOC_MAPK_MEF2A_6 | 753 | 761 | PF00069 | 0.466 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 828 | 831 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 161 | 164 | PF00568 | 0.678 |
DOC_PP4_FxxP_1 | 62 | 65 | PF00568 | 0.568 |
DOC_SPAK_OSR1_1 | 642 | 646 | PF12202 | 0.321 |
DOC_USP7_MATH_1 | 1058 | 1062 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 862 | 866 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 868 | 872 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 903 | 907 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 1056 | 1061 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 798 | 803 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 967 | 972 | PF00397 | 0.695 |
LIG_14-3-3_CanoR_1 | 1025 | 1035 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 1065 | 1069 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 192 | 199 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 36 | 45 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 388 | 394 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 588 | 593 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 670 | 680 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 742 | 747 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 814 | 819 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 1011 | 1029 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 1091 | 1108 | PF00022 | 0.510 |
LIG_Actin_WH2_2 | 971 | 986 | PF00022 | 0.516 |
LIG_BIR_III_2 | 1057 | 1061 | PF00653 | 0.562 |
LIG_BIR_III_2 | 176 | 180 | PF00653 | 0.688 |
LIG_BIR_III_4 | 578 | 582 | PF00653 | 0.356 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.682 |
LIG_Clathr_ClatBox_1 | 99 | 103 | PF01394 | 0.613 |
LIG_deltaCOP1_diTrp_1 | 609 | 616 | PF00928 | 0.420 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.664 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.692 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.595 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.351 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.468 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.451 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.383 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.505 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.522 |
LIG_FHA_1 | 813 | 819 | PF00498 | 0.547 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.660 |
LIG_FHA_2 | 1069 | 1075 | PF00498 | 0.446 |
LIG_FHA_2 | 1087 | 1093 | PF00498 | 0.323 |
LIG_FHA_2 | 921 | 927 | PF00498 | 0.768 |
LIG_FHA_2 | 959 | 965 | PF00498 | 0.619 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.595 |
LIG_Integrin_RGD_1 | 605 | 607 | PF01839 | 0.245 |
LIG_IRF3_LxIS_1 | 89 | 95 | PF10401 | 0.500 |
LIG_LIR_Apic_2 | 609 | 614 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 61 | 65 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 1004 | 1010 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 575 | 585 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 713 | 721 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 1004 | 1008 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 575 | 580 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 641 | 646 | PF02991 | 0.321 |
LIG_LYPXL_SIV_4 | 438 | 446 | PF13949 | 0.427 |
LIG_PDZ_Class_3 | 1104 | 1109 | PF00595 | 0.491 |
LIG_Pex14_1 | 1078 | 1082 | PF04695 | 0.508 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.427 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.643 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 453 | 456 | PF00017 | 0.380 |
LIG_SH2_SRC | 781 | 784 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 781 | 785 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 832 | 835 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 812 | 815 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 874 | 877 | PF00017 | 0.402 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.564 |
LIG_SH3_3 | 751 | 757 | PF00018 | 0.614 |
LIG_SH3_3 | 993 | 999 | PF00018 | 0.716 |
LIG_SUMO_SIM_par_1 | 46 | 51 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 682 | 689 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 767 | 773 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 90 | 97 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 977 | 982 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.511 |
LIG_TRAF2_1 | 1090 | 1093 | PF00917 | 0.512 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.680 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.442 |
LIG_TRAF2_1 | 940 | 943 | PF00917 | 0.753 |
LIG_TYR_ITIM | 393 | 398 | PF00017 | 0.420 |
LIG_TYR_ITIM | 451 | 456 | PF00017 | 0.420 |
MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.612 |
MOD_CDK_SPxxK_3 | 759 | 766 | PF00069 | 0.404 |
MOD_CK1_1 | 1059 | 1065 | PF00069 | 0.549 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.660 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.670 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.676 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.446 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.267 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.604 |
MOD_CK1_1 | 801 | 807 | PF00069 | 0.679 |
MOD_CK1_1 | 906 | 912 | PF00069 | 0.674 |
MOD_CK2_1 | 1068 | 1074 | PF00069 | 0.451 |
MOD_CK2_1 | 1086 | 1092 | PF00069 | 0.321 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.510 |
MOD_CK2_1 | 770 | 776 | PF00069 | 0.507 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.519 |
MOD_Cter_Amidation | 517 | 520 | PF01082 | 0.356 |
MOD_Cter_Amidation | 534 | 537 | PF01082 | 0.180 |
MOD_GlcNHglycan | 1086 | 1089 | PF01048 | 0.529 |
MOD_GlcNHglycan | 1098 | 1101 | PF01048 | 0.490 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.621 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.727 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.750 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.742 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.681 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.457 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.441 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.492 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.505 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.526 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.516 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.556 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.558 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.624 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.762 |
MOD_GlcNHglycan | 864 | 867 | PF01048 | 0.387 |
MOD_GlcNHglycan | 986 | 989 | PF01048 | 0.626 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.568 |
MOD_GSK3_1 | 1064 | 1071 | PF00069 | 0.541 |
MOD_GSK3_1 | 1082 | 1089 | PF00069 | 0.478 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.707 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.665 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.733 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.605 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.662 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.643 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.679 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.502 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.566 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.635 |
MOD_GSK3_1 | 903 | 910 | PF00069 | 0.668 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.693 |
MOD_GSK3_1 | 950 | 957 | PF00069 | 0.732 |
MOD_GSK3_1 | 959 | 966 | PF00069 | 0.637 |
MOD_GSK3_1 | 979 | 986 | PF00069 | 0.538 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.601 |
MOD_NEK2_1 | 1008 | 1013 | PF00069 | 0.582 |
MOD_NEK2_1 | 1026 | 1031 | PF00069 | 0.434 |
MOD_NEK2_1 | 1082 | 1087 | PF00069 | 0.434 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.620 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.548 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.585 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.677 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.660 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.427 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.647 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.440 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.427 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.589 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.522 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.626 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.606 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.681 |
MOD_NEK2_2 | 1068 | 1073 | PF00069 | 0.439 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.245 |
MOD_NEK2_2 | 597 | 602 | PF00069 | 0.427 |
MOD_NEK2_2 | 748 | 753 | PF00069 | 0.544 |
MOD_NEK2_2 | 781 | 786 | PF00069 | 0.401 |
MOD_OFUCOSY | 811 | 816 | PF10250 | 0.497 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.579 |
MOD_PIKK_1 | 830 | 836 | PF00454 | 0.627 |
MOD_PIKK_1 | 920 | 926 | PF00454 | 0.770 |
MOD_PKA_1 | 1027 | 1033 | PF00069 | 0.491 |
MOD_PKA_1 | 742 | 748 | PF00069 | 0.486 |
MOD_PKA_2 | 1026 | 1032 | PF00069 | 0.466 |
MOD_PKA_2 | 1064 | 1070 | PF00069 | 0.476 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.751 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.721 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.607 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.400 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.377 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.463 |
MOD_PKA_2 | 950 | 956 | PF00069 | 0.601 |
MOD_PKA_2 | 983 | 989 | PF00069 | 0.590 |
MOD_PKB_1 | 1025 | 1033 | PF00069 | 0.535 |
MOD_PKB_1 | 1094 | 1102 | PF00069 | 0.353 |
MOD_PKB_1 | 586 | 594 | PF00069 | 0.245 |
MOD_Plk_1 | 1006 | 1012 | PF00069 | 0.463 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.568 |
MOD_Plk_1 | 668 | 674 | PF00069 | 0.320 |
MOD_Plk_2-3 | 959 | 965 | PF00069 | 0.708 |
MOD_Plk_4 | 1034 | 1040 | PF00069 | 0.435 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.588 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.607 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.321 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.245 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.422 |
MOD_ProDKin_1 | 1056 | 1062 | PF00069 | 0.618 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.548 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.675 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.507 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.574 |
MOD_ProDKin_1 | 798 | 804 | PF00069 | 0.629 |
MOD_ProDKin_1 | 967 | 973 | PF00069 | 0.688 |
MOD_SUMO_for_1 | 440 | 443 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 937 | 945 | PF00179 | 0.628 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.587 |
TRG_DiLeu_BaEn_1 | 489 | 494 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_1 | 542 | 547 | PF01217 | 0.420 |
TRG_DiLeu_BaEn_3 | 1092 | 1098 | PF01217 | 0.501 |
TRG_DiLeu_BaEn_3 | 338 | 344 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 651 | 656 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.700 |
TRG_DiLeu_LyEn_5 | 365 | 370 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 1013 | 1016 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 1024 | 1027 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 1094 | 1097 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 752 | 755 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 843 | 846 | PF00400 | 0.707 |
TRG_NES_CRM1_1 | 46 | 61 | PF08389 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 613 | 617 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 670 | 675 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L8 | Leptomonas seymouri | 46% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 28% | 100% |
A0A422NGS3 | Trypanosoma rangeli | 32% | 100% |
A4H397 | Leishmania braziliensis | 69% | 99% |
A4HRI7 | Leishmania infantum | 99% | 100% |
C9ZXL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AC55 | Leishmania major | 88% | 100% |
E9AJF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 98% |
V5DD81 | Trypanosoma cruzi | 30% | 100% |