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: 5 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005788 | endoplasmic reticulum lumen | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
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: E9AJF1
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 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0044183 | protein folding chaperone | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
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 | 1084 | 1088 | PF00656 | 0.278 |
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 791 | 795 | PF00656 | 0.610 |
CLV_MEL_PAP_1 | 988 | 994 | PF00089 | 0.678 |
CLV_NRD_NRD_1 | 1020 | 1022 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 827 | 829 | PF00675 | 0.397 |
CLV_PCSK_FUR_1 | 28 | 32 | PF00082 | 0.373 |
CLV_PCSK_FUR_1 | 312 | 316 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 1020 | 1022 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.669 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.445 |
CLV_PCSK_PC7_1 | 521 | 527 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 1103 | 1107 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 1109 | 1113 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.564 |
DEG_APCC_DBOX_1 | 758 | 766 | PF00400 | 0.632 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.581 |
DEG_SCF_TRCP1_1 | 167 | 173 | PF00400 | 0.422 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.296 |
DOC_ANK_TNKS_1 | 647 | 654 | PF00023 | 0.280 |
DOC_ANK_TNKS_1 | 947 | 954 | PF00023 | 0.431 |
DOC_CKS1_1 | 840 | 845 | PF01111 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 404 | 410 | PF00134 | 0.364 |
DOC_MAPK_DCC_7 | 148 | 156 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 453 | 462 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 848 | 856 | PF00069 | 0.687 |
DOC_MAPK_HePTP_8 | 288 | 300 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 291 | 300 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 855 | 863 | PF00069 | 0.202 |
DOC_MAPK_MEF2A_6 | 984 | 992 | PF00069 | 0.401 |
DOC_MAPK_RevD_3 | 52 | 68 | PF00069 | 0.260 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.323 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.250 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.494 |
DOC_SPAK_OSR1_1 | 648 | 652 | PF12202 | 0.280 |
DOC_USP7_MATH_1 | 1065 | 1069 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 804 | 808 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 843 | 847 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 873 | 877 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 908 | 912 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 1063 | 1068 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 839 | 844 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 962 | 967 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 1032 | 1042 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 1073 | 1082 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 190 | 197 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 366 | 375 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 394 | 401 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 431 | 441 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 748 | 753 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 803 | 811 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 820 | 825 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 1018 | 1036 | PF00022 | 0.456 |
LIG_Actin_WH2_2 | 1098 | 1115 | PF00022 | 0.430 |
LIG_Actin_WH2_2 | 976 | 993 | PF00022 | 0.419 |
LIG_APCC_Cbox_1 | 520 | 526 | PF00515 | 0.193 |
LIG_BIR_III_2 | 1064 | 1068 | PF00653 | 0.454 |
LIG_BIR_III_2 | 174 | 178 | PF00653 | 0.553 |
LIG_BIR_III_4 | 584 | 588 | PF00653 | 0.318 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 615 | 622 | PF00928 | 0.364 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.552 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.581 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.301 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.364 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.687 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.609 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.630 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.526 |
LIG_FHA_2 | 1076 | 1082 | PF00498 | 0.376 |
LIG_FHA_2 | 1094 | 1100 | PF00498 | 0.301 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.452 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.507 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.390 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.233 |
LIG_FHA_2 | 789 | 795 | PF00498 | 0.600 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.462 |
LIG_FHA_2 | 926 | 932 | PF00498 | 0.540 |
LIG_LIR_Apic_2 | 615 | 620 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 776 | 781 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 581 | 591 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 581 | 586 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.280 |
LIG_LYPXL_SIV_4 | 444 | 452 | PF13949 | 0.323 |
LIG_MLH1_MIPbox_1 | 69 | 73 | PF16413 | 0.440 |
LIG_PCNA_yPIPBox_3 | 1009 | 1023 | PF02747 | 0.287 |
LIG_PDZ_Class_3 | 1111 | 1116 | PF00595 | 0.415 |
LIG_Pex14_1 | 518 | 522 | PF04695 | 0.323 |
LIG_Rb_LxCxE_1 | 224 | 243 | PF01857 | 0.390 |
LIG_REV1ctd_RIR_1 | 70 | 79 | PF16727 | 0.447 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.323 |
LIG_SH2_PTP2 | 459 | 462 | PF00017 | 0.323 |
LIG_SH2_SRC | 787 | 790 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 818 | 821 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 879 | 882 | PF00017 | 0.352 |
LIG_SH3_1 | 8 | 14 | PF00018 | 0.630 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.447 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.496 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.653 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.630 |
LIG_SH3_3 | 963 | 969 | PF00018 | 0.449 |
LIG_SUMO_SIM_par_1 | 46 | 51 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 688 | 695 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 771 | 779 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 86 | 94 | PF11976 | 0.498 |
LIG_TRAF2_1 | 1097 | 1100 | PF00917 | 0.387 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.420 |
LIG_TRAF2_1 | 937 | 940 | PF00917 | 0.634 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.441 |
LIG_TYR_ITIM | 457 | 462 | PF00017 | 0.441 |
MOD_CDK_SPxxK_3 | 173 | 180 | PF00069 | 0.628 |
MOD_CK1_1 | 1066 | 1072 | PF00069 | 0.572 |
MOD_CK1_1 | 1094 | 1100 | PF00069 | 0.521 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.607 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.691 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.268 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.578 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.658 |
MOD_CK1_1 | 807 | 813 | PF00069 | 0.451 |
MOD_CK1_1 | 970 | 976 | PF00069 | 0.662 |
MOD_CK2_1 | 1075 | 1081 | PF00069 | 0.462 |
MOD_CK2_1 | 1093 | 1099 | PF00069 | 0.347 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.573 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.606 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.707 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.558 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.475 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.468 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.580 |
MOD_CK2_1 | 935 | 941 | PF00069 | 0.662 |
MOD_Cter_Amidation | 26 | 29 | PF01082 | 0.506 |
MOD_Cter_Amidation | 523 | 526 | PF01082 | 0.377 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.648 |
MOD_GlcNHglycan | 1093 | 1096 | PF01048 | 0.489 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.604 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.666 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.660 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.689 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.561 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.396 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.492 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.479 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.381 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.524 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.466 |
MOD_GlcNHglycan | 784 | 787 | PF01048 | 0.513 |
MOD_GlcNHglycan | 800 | 803 | PF01048 | 0.677 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.432 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.753 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.419 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.694 |
MOD_GlcNHglycan | 993 | 996 | PF01048 | 0.630 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.551 |
MOD_GSK3_1 | 1071 | 1078 | PF00069 | 0.501 |
MOD_GSK3_1 | 1089 | 1096 | PF00069 | 0.624 |
MOD_GSK3_1 | 1103 | 1110 | PF00069 | 0.447 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.712 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.634 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.629 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.678 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.715 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.560 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.263 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.329 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.556 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.334 |
MOD_GSK3_1 | 839 | 846 | PF00069 | 0.662 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.703 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.728 |
MOD_GSK3_1 | 956 | 963 | PF00069 | 0.611 |
MOD_GSK3_1 | 991 | 998 | PF00069 | 0.598 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.587 |
MOD_N-GLC_1 | 812 | 817 | PF02516 | 0.626 |
MOD_N-GLC_1 | 935 | 940 | PF02516 | 0.604 |
MOD_NEK2_1 | 1015 | 1020 | PF00069 | 0.559 |
MOD_NEK2_1 | 1033 | 1038 | PF00069 | 0.336 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.628 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.579 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.702 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.683 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.390 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.498 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.377 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.258 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.202 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.383 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.260 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.567 |
MOD_NEK2_1 | 990 | 995 | PF00069 | 0.598 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.663 |
MOD_NEK2_2 | 1075 | 1080 | PF00069 | 0.449 |
MOD_NEK2_2 | 603 | 608 | PF00069 | 0.383 |
MOD_NEK2_2 | 754 | 759 | PF00069 | 0.506 |
MOD_OFUCOSY | 817 | 822 | PF10250 | 0.516 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.572 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.404 |
MOD_PIKK_1 | 836 | 842 | PF00454 | 0.696 |
MOD_PIKK_1 | 925 | 931 | PF00454 | 0.692 |
MOD_PIKK_1 | 970 | 976 | PF00454 | 0.759 |
MOD_PK_1 | 274 | 280 | PF00069 | 0.526 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.600 |
MOD_PKA_1 | 748 | 754 | PF00069 | 0.482 |
MOD_PKA_2 | 1033 | 1039 | PF00069 | 0.486 |
MOD_PKA_2 | 1075 | 1081 | PF00069 | 0.436 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.629 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.605 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.621 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.370 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.357 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.273 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.600 |
MOD_PKA_2 | 747 | 753 | PF00069 | 0.570 |
MOD_PKA_2 | 947 | 953 | PF00069 | 0.630 |
MOD_PKA_2 | 990 | 996 | PF00069 | 0.640 |
MOD_PKB_1 | 1032 | 1040 | PF00069 | 0.545 |
MOD_PKB_1 | 1101 | 1109 | PF00069 | 0.378 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.573 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.620 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.334 |
MOD_Plk_1 | 908 | 914 | PF00069 | 0.595 |
MOD_Plk_2-3 | 956 | 962 | PF00069 | 0.730 |
MOD_Plk_4 | 1041 | 1047 | PF00069 | 0.519 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.669 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.383 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.544 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.391 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.399 |
MOD_ProDKin_1 | 1063 | 1069 | PF00069 | 0.663 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.584 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.635 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.544 |
MOD_ProDKin_1 | 839 | 845 | PF00069 | 0.490 |
MOD_ProDKin_1 | 962 | 968 | PF00069 | 0.674 |
MOD_SUMO_for_1 | 446 | 449 | PF00179 | 0.383 |
MOD_SUMO_for_1 | 765 | 768 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.675 |
TRG_DiLeu_BaEn_1 | 495 | 500 | PF01217 | 0.318 |
TRG_DiLeu_BaEn_1 | 548 | 553 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_3 | 1099 | 1105 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_3 | 344 | 350 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 657 | 662 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.669 |
TRG_DiLeu_LyEn_5 | 371 | 376 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.723 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 1020 | 1023 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 1031 | 1034 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 1101 | 1104 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 525 | 527 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.636 |
TRG_NES_CRM1_1 | 46 | 61 | PF08389 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 366 | 370 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 619 | 623 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 756 | 761 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L8 | Leptomonas seymouri | 47% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 29% | 100% |
A0A3S5H4W3 | Leishmania donovani | 82% | 100% |
A4H397 | Leishmania braziliensis | 68% | 100% |
A4HRI7 | Leishmania infantum | 81% | 100% |
E9AC55 | Leishmania major | 80% | 98% |