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. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 6 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005788 | endoplasmic reticulum lumen | 5 | 2 |
GO:0016020 | membrane | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0034663 | endoplasmic reticulum chaperone complex | 3 | 2 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9AC55
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 2 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006986 | response to unfolded protein | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010033 | response to organic substance | 3 | 2 |
GO:0010243 | response to organonitrogen compound | 4 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 2 |
GO:0030968 | endoplasmic reticulum unfolded protein response | 3 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034620 | cellular response to unfolded protein | 5 | 2 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 2 |
GO:0035966 | response to topologically incorrect protein | 3 | 2 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 2 |
GO:0036503 | ERAD pathway | 5 | 2 |
GO:0042026 | protein refolding | 3 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 2 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0061077 | chaperone-mediated protein folding | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070887 | cellular response to chemical stimulus | 3 | 2 |
GO:0071310 | cellular response to organic substance | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901698 | response to nitrogen compound | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0031072 | heat shock protein binding | 3 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0044183 | protein folding chaperone | 1 | 9 |
GO:0051082 | unfolded protein binding | 3 | 2 |
GO:0051787 | misfolded protein binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 789 | 793 | PF00656 | 0.462 |
CLV_MEL_PAP_1 | 984 | 990 | PF00089 | 0.512 |
CLV_NRD_NRD_1 | 1016 | 1018 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 1030 | 1032 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 849 | 851 | PF00675 | 0.679 |
CLV_PCSK_FUR_1 | 1028 | 1032 | PF00082 | 0.463 |
CLV_PCSK_FUR_1 | 847 | 851 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 1016 | 1018 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 1030 | 1032 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 849 | 851 | PF00082 | 0.733 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 518 | 524 | PF00082 | 0.348 |
CLV_PCSK_PC7_1 | 535 | 541 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 1105 | 1109 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.348 |
DEG_APCC_DBOX_1 | 756 | 764 | PF00400 | 0.463 |
DEG_SCF_FBW7_1 | 956 | 961 | PF00400 | 0.544 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 430 | 434 | PF00917 | 0.339 |
DOC_ANK_TNKS_1 | 644 | 651 | PF00023 | 0.283 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 407 | PF00134 | 0.348 |
DOC_MAPK_DCC_7 | 149 | 157 | PF00069 | 0.639 |
DOC_MAPK_DCC_7 | 757 | 765 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 65 | 72 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 757 | 765 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 847 | 855 | PF00069 | 0.589 |
DOC_MAPK_HePTP_8 | 291 | 303 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 149 | 157 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 294 | 303 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 757 | 765 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 980 | 988 | PF00069 | 0.464 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.377 |
DOC_PP2B_LxvP_1 | 474 | 477 | PF13499 | 0.238 |
DOC_PP2B_LxvP_1 | 832 | 835 | PF13499 | 0.416 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.519 |
DOC_SPAK_OSR1_1 | 645 | 649 | PF12202 | 0.283 |
DOC_USP7_MATH_1 | 1061 | 1065 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 796 | 800 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 866 | 870 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 872 | 876 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 1059 | 1064 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 802 | 807 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 954 | 959 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 969 | 974 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 1028 | 1038 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 1069 | 1078 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 377 | 383 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 391 | 398 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 428 | 438 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 673 | 683 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 818 | 823 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 1014 | 1032 | PF00022 | 0.477 |
LIG_Actin_WH2_2 | 1094 | 1111 | PF00022 | 0.437 |
LIG_BIR_III_2 | 1060 | 1064 | PF00653 | 0.507 |
LIG_BIR_III_2 | 175 | 179 | PF00653 | 0.630 |
LIG_BIR_III_4 | 581 | 585 | PF00653 | 0.304 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.603 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.442 |
LIG_Clathr_ClatBox_1 | 98 | 102 | PF01394 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 612 | 619 | PF00928 | 0.348 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.648 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.496 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.607 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.569 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.352 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.643 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.300 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.528 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.455 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.434 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.615 |
LIG_FHA_2 | 1072 | 1078 | PF00498 | 0.382 |
LIG_FHA_2 | 1090 | 1096 | PF00498 | 0.307 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.669 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.552 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.252 |
LIG_FHA_2 | 787 | 793 | PF00498 | 0.450 |
LIG_FHA_2 | 925 | 931 | PF00498 | 0.752 |
LIG_Integrin_RGD_1 | 488 | 490 | PF01839 | 0.217 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.520 |
LIG_LIR_Apic_2 | 612 | 617 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 1007 | 1013 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 455 | 462 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 578 | 588 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 716 | 724 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 1007 | 1011 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 578 | 583 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 644 | 649 | PF02991 | 0.283 |
LIG_LYPXL_SIV_4 | 441 | 449 | PF13949 | 0.377 |
LIG_MLH1_MIPbox_1 | 68 | 72 | PF16413 | 0.493 |
LIG_PDZ_Class_3 | 1107 | 1112 | PF00595 | 0.440 |
LIG_Pex14_1 | 515 | 519 | PF04695 | 0.377 |
LIG_REV1ctd_RIR_1 | 69 | 78 | PF16727 | 0.499 |
LIG_RPA_C_Fungi | 283 | 295 | PF08784 | 0.524 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.598 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.559 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 456 | 459 | PF00017 | 0.317 |
LIG_SH2_SRC | 785 | 788 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 472 | 476 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 836 | 839 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.742 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 816 | 819 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 836 | 839 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 878 | 881 | PF00017 | 0.443 |
LIG_SH3_1 | 8 | 14 | PF00018 | 0.522 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.478 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.567 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.540 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.559 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.522 |
LIG_SUMO_SIM_par_1 | 45 | 50 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 685 | 692 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 771 | 777 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 89 | 96 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 97 | 102 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 980 | 985 | PF11976 | 0.479 |
LIG_TRAF2_1 | 1093 | 1096 | PF00917 | 0.453 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.645 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.349 |
LIG_TRAF2_1 | 944 | 947 | PF00917 | 0.810 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.348 |
LIG_TYR_ITIM | 454 | 459 | PF00017 | 0.348 |
LIG_UBA3_1 | 372 | 378 | PF00899 | 0.546 |
MOD_CDK_SPK_2 | 954 | 959 | PF00069 | 0.550 |
MOD_CK1_1 | 1062 | 1068 | PF00069 | 0.484 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.630 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.616 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.604 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.400 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.629 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.567 |
MOD_CK2_1 | 1071 | 1077 | PF00069 | 0.387 |
MOD_CK2_1 | 1089 | 1095 | PF00069 | 0.302 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.630 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.569 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.460 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.526 |
MOD_CK2_1 | 774 | 780 | PF00069 | 0.469 |
MOD_Cter_Amidation | 520 | 523 | PF01082 | 0.389 |
MOD_GlcNHglycan | 1089 | 1092 | PF01048 | 0.475 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.571 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.712 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.591 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.690 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.761 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.665 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.615 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.543 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.377 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.427 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.348 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.470 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.505 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.467 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.511 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.657 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.762 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.394 |
MOD_GlcNHglycan | 989 | 992 | PF01048 | 0.651 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.478 |
MOD_GSK3_1 | 1067 | 1074 | PF00069 | 0.618 |
MOD_GSK3_1 | 1085 | 1092 | PF00069 | 0.408 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.685 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.672 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.662 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.753 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.716 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.510 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.614 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.225 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.516 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.530 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.632 |
MOD_GSK3_1 | 907 | 914 | PF00069 | 0.680 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.652 |
MOD_GSK3_1 | 954 | 961 | PF00069 | 0.727 |
MOD_GSK3_1 | 963 | 970 | PF00069 | 0.608 |
MOD_GSK3_1 | 982 | 989 | PF00069 | 0.510 |
MOD_N-GLC_1 | 810 | 815 | PF02516 | 0.572 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.524 |
MOD_NEK2_1 | 1011 | 1016 | PF00069 | 0.467 |
MOD_NEK2_1 | 1029 | 1034 | PF00069 | 0.305 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.540 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.686 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.650 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.605 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.503 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.407 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.550 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.304 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.281 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.377 |
MOD_NEK2_1 | 724 | 729 | PF00069 | 0.494 |
MOD_NEK2_1 | 986 | 991 | PF00069 | 0.582 |
MOD_NEK2_2 | 104 | 109 | PF00069 | 0.593 |
MOD_NEK2_2 | 1071 | 1076 | PF00069 | 0.376 |
MOD_NEK2_2 | 600 | 605 | PF00069 | 0.377 |
MOD_NEK2_2 | 752 | 757 | PF00069 | 0.495 |
MOD_OFUCOSY | 815 | 820 | PF10250 | 0.434 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.339 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.217 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.562 |
MOD_PIKK_1 | 924 | 930 | PF00454 | 0.737 |
MOD_PKA_1 | 1030 | 1036 | PF00069 | 0.430 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.534 |
MOD_PKA_1 | 746 | 752 | PF00069 | 0.531 |
MOD_PKA_2 | 1029 | 1035 | PF00069 | 0.492 |
MOD_PKA_2 | 1071 | 1077 | PF00069 | 0.369 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.777 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.635 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.349 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.291 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.377 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.323 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.535 |
MOD_PKA_2 | 745 | 751 | PF00069 | 0.508 |
MOD_PKA_2 | 986 | 992 | PF00069 | 0.524 |
MOD_PKB_1 | 1028 | 1036 | PF00069 | 0.463 |
MOD_Plk_1 | 1009 | 1015 | PF00069 | 0.405 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.630 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.475 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.391 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.283 |
MOD_Plk_2-3 | 963 | 969 | PF00069 | 0.751 |
MOD_Plk_4 | 1037 | 1043 | PF00069 | 0.498 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.593 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.316 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.355 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.493 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.482 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.506 |
MOD_ProDKin_1 | 1059 | 1065 | PF00069 | 0.545 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.547 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.599 |
MOD_ProDKin_1 | 802 | 808 | PF00069 | 0.567 |
MOD_ProDKin_1 | 954 | 960 | PF00069 | 0.590 |
MOD_ProDKin_1 | 969 | 975 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 443 | 446 | PF00179 | 0.377 |
MOD_SUMO_rev_2 | 946 | 952 | PF00179 | 0.604 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.573 |
TRG_DiLeu_BaEn_1 | 545 | 550 | PF01217 | 0.348 |
TRG_DiLeu_BaEn_3 | 1095 | 1101 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_3 | 341 | 347 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 654 | 659 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.661 |
TRG_DiLeu_LyEn_5 | 368 | 373 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 719 | 722 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 1016 | 1019 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 1027 | 1030 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 1097 | 1100 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.217 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 756 | 759 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 847 | 850 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 852 | 855 | PF00400 | 0.596 |
TRG_NES_CRM1_1 | 45 | 60 | PF08389 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 616 | 620 | PF00026 | 0.348 |
TRG_Pf-PMV_PEXEL_1 | 673 | 678 | PF00026 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L8 | Leptomonas seymouri | 47% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 29% | 100% |
A0A3S5H4W3 | Leishmania donovani | 88% | 100% |
A0A422NGS3 | Trypanosoma rangeli | 30% | 100% |
A4H397 | Leishmania braziliensis | 69% | 99% |
A4HRI7 | Leishmania infantum | 87% | 100% |
E9AJF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |