Appears to be a secreted chaperone, related to mammalian HYOU1 proteins. Probably ER-localized as in other eukaryotes
Chaperone/Protein Folding, HSP70-like
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: 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: A4HRI7
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 | 128 | 132 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 962 | 966 | PF00656 | 0.669 |
CLV_MEL_PAP_1 | 982 | 988 | PF00089 | 0.559 |
CLV_NRD_NRD_1 | 1014 | 1016 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 1028 | 1030 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 1066 | 1068 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 822 | 824 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 846 | 848 | PF00675 | 0.653 |
CLV_PCSK_FUR_1 | 1026 | 1030 | PF00082 | 0.554 |
CLV_PCSK_FUR_1 | 844 | 848 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 1014 | 1016 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 1028 | 1030 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 1066 | 1068 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 846 | 848 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 516 | 522 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 533 | 539 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 1103 | 1107 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 753 | 761 | PF00400 | 0.509 |
DEG_APCC_KENBOX_2 | 1043 | 1047 | PF00400 | 0.345 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.690 |
DOC_ANK_TNKS_1 | 642 | 649 | PF00023 | 0.321 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 57 | 63 | PF00134 | 0.416 |
DOC_MAPK_DCC_7 | 151 | 159 | PF00069 | 0.690 |
DOC_MAPK_DCC_7 | 754 | 762 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 151 | 159 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 448 | 457 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 754 | 762 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 844 | 852 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 151 | 159 | PF00069 | 0.690 |
DOC_MAPK_MEF2A_6 | 754 | 762 | PF00069 | 0.460 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 829 | 832 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.680 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.572 |
DOC_SPAK_OSR1_1 | 643 | 647 | PF12202 | 0.321 |
DOC_USP7_MATH_1 | 1059 | 1063 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 731 | 735 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 863 | 867 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 869 | 873 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 904 | 908 | PF00917 | 0.736 |
DOC_WW_Pin1_4 | 1057 | 1062 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 799 | 804 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 968 | 973 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 1026 | 1036 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 1066 | 1070 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 193 | 200 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 389 | 395 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 426 | 436 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 589 | 594 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 671 | 681 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 743 | 748 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 815 | 820 | PF00244 | 0.399 |
LIG_Actin_WH2_2 | 1012 | 1030 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 1092 | 1109 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 972 | 987 | PF00022 | 0.502 |
LIG_BIR_III_2 | 1058 | 1062 | PF00653 | 0.537 |
LIG_BIR_III_2 | 177 | 181 | PF00653 | 0.680 |
LIG_BIR_III_4 | 579 | 583 | PF00653 | 0.356 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.680 |
LIG_Clathr_ClatBox_1 | 100 | 104 | PF01394 | 0.473 |
LIG_deltaCOP1_diTrp_1 | 610 | 617 | PF00928 | 0.420 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.665 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.704 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.653 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.351 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.420 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.624 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.303 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.502 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.492 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.483 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.569 |
LIG_FHA_2 | 1070 | 1076 | PF00498 | 0.441 |
LIG_FHA_2 | 1088 | 1094 | PF00498 | 0.314 |
LIG_FHA_2 | 922 | 928 | PF00498 | 0.778 |
LIG_FHA_2 | 960 | 966 | PF00498 | 0.619 |
LIG_Integrin_RGD_1 | 183 | 185 | PF01839 | 0.584 |
LIG_Integrin_RGD_1 | 606 | 608 | PF01839 | 0.245 |
LIG_IRF3_LxIS_1 | 90 | 96 | PF10401 | 0.499 |
LIG_LIR_Apic_2 | 610 | 615 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 62 | 66 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 1005 | 1011 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 393 | 403 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 42 | 53 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 576 | 586 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 714 | 722 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 1005 | 1009 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 576 | 581 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.321 |
LIG_LYPXL_SIV_4 | 439 | 447 | PF13949 | 0.427 |
LIG_PDZ_Class_3 | 1105 | 1110 | PF00595 | 0.482 |
LIG_Pex14_1 | 1079 | 1083 | PF04695 | 0.505 |
LIG_Pex14_1 | 513 | 517 | PF04695 | 0.427 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.644 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 470 | 474 | PF00017 | 0.407 |
LIG_SH2_PTP2 | 454 | 457 | PF00017 | 0.380 |
LIG_SH2_SRC | 782 | 785 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.689 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 782 | 786 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 833 | 836 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 875 | 878 | PF00017 | 0.399 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.555 |
LIG_SH3_3 | 752 | 758 | PF00018 | 0.589 |
LIG_SH3_3 | 994 | 1000 | PF00018 | 0.689 |
LIG_SUMO_SIM_par_1 | 47 | 52 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 683 | 690 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 768 | 774 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 91 | 98 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 978 | 983 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 99 | 104 | PF11976 | 0.377 |
LIG_TRAF2_1 | 1091 | 1094 | PF00917 | 0.509 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.676 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.476 |
LIG_TRAF2_1 | 941 | 944 | PF00917 | 0.762 |
LIG_TRFH_1 | 56 | 60 | PF08558 | 0.410 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.420 |
LIG_TYR_ITIM | 452 | 457 | PF00017 | 0.420 |
MOD_CDK_SPxxK_3 | 176 | 183 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 760 | 767 | PF00069 | 0.397 |
MOD_CK1_1 | 1060 | 1066 | PF00069 | 0.543 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.664 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.657 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.623 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.433 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.285 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.599 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.673 |
MOD_CK1_1 | 907 | 913 | PF00069 | 0.662 |
MOD_CK2_1 | 1069 | 1075 | PF00069 | 0.445 |
MOD_CK2_1 | 1087 | 1093 | PF00069 | 0.310 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.529 |
MOD_CK2_1 | 771 | 777 | PF00069 | 0.520 |
MOD_Cter_Amidation | 518 | 521 | PF01082 | 0.356 |
MOD_Cter_Amidation | 535 | 538 | PF01082 | 0.180 |
MOD_GlcNHglycan | 1087 | 1090 | PF01048 | 0.509 |
MOD_GlcNHglycan | 1099 | 1102 | PF01048 | 0.488 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.618 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.704 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.717 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.510 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.681 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.436 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.458 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.498 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.531 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.521 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.545 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.611 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.703 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.777 |
MOD_GlcNHglycan | 865 | 868 | PF01048 | 0.383 |
MOD_GlcNHglycan | 987 | 990 | PF01048 | 0.618 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.516 |
MOD_GSK3_1 | 1065 | 1072 | PF00069 | 0.551 |
MOD_GSK3_1 | 1083 | 1090 | PF00069 | 0.494 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.695 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.665 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.711 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.588 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.627 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.686 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.654 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.467 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.500 |
MOD_GSK3_1 | 831 | 838 | PF00069 | 0.645 |
MOD_GSK3_1 | 904 | 911 | PF00069 | 0.667 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.613 |
MOD_GSK3_1 | 951 | 958 | PF00069 | 0.726 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.637 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.531 |
MOD_NEK2_1 | 1009 | 1014 | PF00069 | 0.524 |
MOD_NEK2_1 | 1027 | 1032 | PF00069 | 0.347 |
MOD_NEK2_1 | 1083 | 1088 | PF00069 | 0.445 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.605 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.537 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.573 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.689 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.653 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.427 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.640 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.421 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.427 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.531 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.523 |
MOD_NEK2_1 | 908 | 913 | PF00069 | 0.594 |
MOD_NEK2_1 | 984 | 989 | PF00069 | 0.599 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.616 |
MOD_NEK2_2 | 1069 | 1074 | PF00069 | 0.433 |
MOD_NEK2_2 | 390 | 395 | PF00069 | 0.245 |
MOD_NEK2_2 | 598 | 603 | PF00069 | 0.427 |
MOD_NEK2_2 | 749 | 754 | PF00069 | 0.546 |
MOD_NEK2_2 | 782 | 787 | PF00069 | 0.403 |
MOD_OFUCOSY | 812 | 817 | PF10250 | 0.495 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.562 |
MOD_PIKK_1 | 831 | 837 | PF00454 | 0.645 |
MOD_PIKK_1 | 921 | 927 | PF00454 | 0.792 |
MOD_PKA_1 | 1028 | 1034 | PF00069 | 0.487 |
MOD_PKA_1 | 743 | 749 | PF00069 | 0.494 |
MOD_PKA_2 | 1027 | 1033 | PF00069 | 0.463 |
MOD_PKA_2 | 1065 | 1071 | PF00069 | 0.450 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.738 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.729 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.648 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.402 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.362 |
MOD_PKA_2 | 742 | 748 | PF00069 | 0.461 |
MOD_PKA_2 | 951 | 957 | PF00069 | 0.596 |
MOD_PKA_2 | 984 | 990 | PF00069 | 0.584 |
MOD_PKB_1 | 1026 | 1034 | PF00069 | 0.532 |
MOD_PKB_1 | 1095 | 1103 | PF00069 | 0.351 |
MOD_PKB_1 | 587 | 595 | PF00069 | 0.245 |
MOD_Plk_1 | 1007 | 1013 | PF00069 | 0.469 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.619 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.313 |
MOD_Plk_2-3 | 960 | 966 | PF00069 | 0.709 |
MOD_Plk_4 | 1035 | 1041 | PF00069 | 0.429 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.595 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.607 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.321 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.245 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.387 |
MOD_ProDKin_1 | 1057 | 1063 | PF00069 | 0.609 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.559 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.608 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.505 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.545 |
MOD_ProDKin_1 | 799 | 805 | PF00069 | 0.624 |
MOD_ProDKin_1 | 968 | 974 | PF00069 | 0.678 |
MOD_SUMO_for_1 | 441 | 444 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 938 | 946 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_1 | 543 | 548 | PF01217 | 0.420 |
TRG_DiLeu_BaEn_3 | 1093 | 1099 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_3 | 339 | 345 | PF01217 | 0.599 |
TRG_DiLeu_BaLyEn_6 | 652 | 657 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.696 |
TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 1014 | 1017 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 1025 | 1028 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 1095 | 1098 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 586 | 589 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 66 | 69 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 753 | 756 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 844 | 847 | PF00400 | 0.697 |
TRG_NES_CRM1_1 | 47 | 62 | PF08389 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 614 | 618 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 671 | 676 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L8 | Leptomonas seymouri | 47% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 28% | 100% |
A0A3S5H4W3 | Leishmania donovani | 99% | 100% |
A0A422NGS3 | Trypanosoma rangeli | 31% | 100% |
A4H397 | Leishmania braziliensis | 69% | 99% |
C9ZXL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AC55 | Leishmania major | 87% | 100% |
E9AJF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 98% |
V5DD81 | Trypanosoma cruzi | 31% | 100% |