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: 3, no: 6 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
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: A4H397
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 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0044183 | protein folding chaperone | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
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 | 158 | 162 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 932 | 936 | PF00656 | 0.450 |
CLV_MEL_PAP_1 | 975 | 981 | PF00089 | 0.643 |
CLV_NRD_NRD_1 | 1007 | 1009 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 1021 | 1023 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.462 |
CLV_PCSK_FUR_1 | 1019 | 1023 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 1007 | 1009 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 1021 | 1023 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.462 |
CLV_PCSK_PC7_1 | 14 | 20 | PF00082 | 0.549 |
CLV_PCSK_PC7_1 | 507 | 513 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 1068 | 1072 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 1108 | 1112 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.501 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.243 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.482 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.266 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.308 |
DEG_SPOP_SBC_1 | 953 | 957 | PF00917 | 0.500 |
DOC_ANK_TNKS_1 | 633 | 640 | PF00023 | 0.292 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.378 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 473 | 480 | PF00134 | 0.191 |
DOC_CYCLIN_yCln2_LP_2 | 390 | 396 | PF00134 | 0.307 |
DOC_MAPK_DCC_7 | 126 | 134 | PF00069 | 0.496 |
DOC_MAPK_DCC_7 | 23 | 32 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 126 | 134 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 439 | 448 | PF00069 | 0.262 |
DOC_MAPK_HePTP_8 | 276 | 288 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 386 | 394 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 971 | 979 | PF00069 | 0.402 |
DOC_MAPK_RevD_3 | 33 | 47 | PF00069 | 0.228 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.267 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.494 |
DOC_SPAK_OSR1_1 | 634 | 638 | PF12202 | 0.267 |
DOC_USP7_MATH_1 | 1048 | 1052 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 1066 | 1070 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 959 | 963 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 1052 | 1057 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 939 | 944 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 954 | 959 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 970 | 975 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 1019 | 1029 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 1079 | 1088 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 170 | 177 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 301 | 309 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 31 | 36 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 417 | 427 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 662 | 672 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 714 | 720 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 796 | 801 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 992 | 996 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 1005 | 1023 | PF00022 | 0.435 |
LIG_Actin_WH2_2 | 1097 | 1114 | PF00022 | 0.387 |
LIG_Actin_WH2_2 | 965 | 980 | PF00022 | 0.456 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 781 | 785 | PF00533 | 0.351 |
LIG_Clathr_ClatBox_1 | 73 | 77 | PF01394 | 0.473 |
LIG_CtBP_PxDLS_1 | 683 | 687 | PF00389 | 0.314 |
LIG_CtBP_PxDLS_1 | 974 | 978 | PF00389 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 1083 | 1088 | PF00928 | 0.275 |
LIG_deltaCOP1_diTrp_1 | 601 | 608 | PF00928 | 0.307 |
LIG_DLG_GKlike_1 | 31 | 38 | PF00625 | 0.205 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.554 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.408 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.363 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.675 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.419 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.395 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.311 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.269 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.545 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.313 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.383 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.515 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.311 |
LIG_FHA_1 | 742 | 748 | PF00498 | 0.404 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.364 |
LIG_FHA_2 | 1093 | 1099 | PF00498 | 0.273 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.431 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.484 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.489 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.468 |
LIG_FHA_2 | 881 | 887 | PF00498 | 0.478 |
LIG_FHA_2 | 903 | 909 | PF00498 | 0.536 |
LIG_FHA_2 | 930 | 936 | PF00498 | 0.478 |
LIG_LIR_Apic_2 | 601 | 606 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 705 | 716 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 705 | 711 | PF02991 | 0.289 |
LIG_LYPXL_SIV_4 | 430 | 438 | PF13949 | 0.332 |
LIG_Pex14_1 | 1084 | 1088 | PF04695 | 0.385 |
LIG_Pex14_1 | 504 | 508 | PF04695 | 0.332 |
LIG_PTB_Apo_2 | 233 | 240 | PF02174 | 0.363 |
LIG_RPA_C_Fungi | 42 | 54 | PF08784 | 0.469 |
LIG_RPA_C_Fungi | 712 | 724 | PF08784 | 0.395 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.403 |
LIG_SH2_GRB2like | 508 | 511 | PF00017 | 0.205 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.205 |
LIG_SH2_NCK_1 | 708 | 712 | PF00017 | 0.273 |
LIG_SH2_PTP2 | 445 | 448 | PF00017 | 0.403 |
LIG_SH2_SRC | 776 | 779 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 794 | 797 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 856 | 859 | PF00017 | 0.422 |
LIG_SH3_3 | 1051 | 1057 | PF00018 | 0.524 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.539 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.558 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.553 |
LIG_SH3_3 | 736 | 742 | PF00018 | 0.455 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.564 |
LIG_SH3_3 | 940 | 946 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 34 | 39 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 36 | 41 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 64 | 72 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 674 | 681 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 760 | 768 | PF11976 | 0.483 |
LIG_TRAF2_1 | 1096 | 1099 | PF00917 | 0.490 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.541 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.359 |
LIG_TRAF2_1 | 904 | 907 | PF00917 | 0.561 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.480 |
LIG_TYR_ITIM | 443 | 448 | PF00017 | 0.394 |
LIG_UBA3_1 | 1032 | 1037 | PF00899 | 0.321 |
LIG_UBA3_1 | 733 | 738 | PF00899 | 0.290 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.272 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.774 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.567 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.408 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.359 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.607 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.529 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.649 |
MOD_CK1_1 | 899 | 905 | PF00069 | 0.625 |
MOD_CK1_1 | 952 | 958 | PF00069 | 0.670 |
MOD_CK1_1 | 981 | 987 | PF00069 | 0.611 |
MOD_CK2_1 | 1092 | 1098 | PF00069 | 0.314 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.541 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.624 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.547 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.665 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.396 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.215 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.597 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.460 |
MOD_CK2_1 | 880 | 886 | PF00069 | 0.658 |
MOD_CK2_1 | 924 | 930 | PF00069 | 0.694 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.773 |
MOD_GlcNHglycan | 1068 | 1071 | PF01048 | 0.478 |
MOD_GlcNHglycan | 1092 | 1095 | PF01048 | 0.524 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.630 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.719 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.636 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.702 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.598 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.754 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.488 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.287 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.554 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.205 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.424 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.406 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.517 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.520 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.476 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.510 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.520 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.742 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.416 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.653 |
MOD_GlcNHglycan | 895 | 899 | PF01048 | 0.669 |
MOD_GlcNHglycan | 951 | 954 | PF01048 | 0.778 |
MOD_GlcNHglycan | 980 | 983 | PF01048 | 0.637 |
MOD_GlcNHglycan | 998 | 1001 | PF01048 | 0.450 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.338 |
MOD_GSK3_1 | 1048 | 1055 | PF00069 | 0.657 |
MOD_GSK3_1 | 1066 | 1073 | PF00069 | 0.607 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.669 |
MOD_GSK3_1 | 1088 | 1095 | PF00069 | 0.604 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.636 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.593 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.649 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.712 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.642 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.596 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.569 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.557 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.249 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.704 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.427 |
MOD_GSK3_1 | 776 | 783 | PF00069 | 0.579 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.581 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.679 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.688 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.545 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.567 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.506 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.540 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.538 |
MOD_N-GLC_1 | 924 | 929 | PF02516 | 0.771 |
MOD_N-GLC_1 | 948 | 953 | PF02516 | 0.622 |
MOD_NEK2_1 | 1002 | 1007 | PF00069 | 0.587 |
MOD_NEK2_1 | 1020 | 1025 | PF00069 | 0.302 |
MOD_NEK2_1 | 1088 | 1093 | PF00069 | 0.405 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.628 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.600 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.561 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.670 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.619 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.299 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.367 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.406 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.413 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.657 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.457 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.672 |
MOD_NEK2_1 | 889 | 894 | PF00069 | 0.608 |
MOD_NEK2_1 | 977 | 982 | PF00069 | 0.565 |
MOD_NEK2_2 | 589 | 594 | PF00069 | 0.403 |
MOD_NEK2_2 | 743 | 748 | PF00069 | 0.502 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.690 |
MOD_OFUCOSY | 793 | 798 | PF10250 | 0.453 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.527 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.579 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.516 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.369 |
MOD_PIKK_1 | 688 | 694 | PF00454 | 0.385 |
MOD_PIKK_1 | 812 | 818 | PF00454 | 0.523 |
MOD_PIKK_1 | 899 | 905 | PF00454 | 0.731 |
MOD_PIKK_1 | 959 | 965 | PF00454 | 0.564 |
MOD_PKA_1 | 1021 | 1027 | PF00069 | 0.458 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.535 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.554 |
MOD_PKA_1 | 580 | 586 | PF00069 | 0.205 |
MOD_PKA_2 | 1020 | 1026 | PF00069 | 0.448 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.535 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.697 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.468 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.571 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.358 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.342 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.471 |
MOD_PKA_2 | 780 | 786 | PF00069 | 0.447 |
MOD_PKA_2 | 977 | 983 | PF00069 | 0.572 |
MOD_PKA_2 | 991 | 997 | PF00069 | 0.396 |
MOD_PKB_1 | 1019 | 1027 | PF00069 | 0.492 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.624 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.540 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.471 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.448 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.287 |
MOD_Plk_1 | 885 | 891 | PF00069 | 0.560 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.475 |
MOD_Plk_4 | 1028 | 1034 | PF00069 | 0.516 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.622 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.630 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.265 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.344 |
MOD_Plk_4 | 672 | 678 | PF00069 | 0.491 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.405 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.764 |
MOD_ProDKin_1 | 1052 | 1058 | PF00069 | 0.672 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.576 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.607 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.588 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.502 |
MOD_ProDKin_1 | 939 | 945 | PF00069 | 0.719 |
MOD_ProDKin_1 | 954 | 960 | PF00069 | 0.777 |
MOD_ProDKin_1 | 970 | 976 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 432 | 435 | PF00179 | 0.403 |
MOD_SUMO_rev_2 | 307 | 317 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 902 | 910 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_1 | 534 | 539 | PF01217 | 0.368 |
TRG_DiLeu_BaEn_3 | 1098 | 1104 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_3 | 322 | 328 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.205 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.693 |
TRG_DiLeu_BaLyEn_6 | 643 | 648 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.679 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 708 | 711 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 1007 | 1010 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 1018 | 1021 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 1100 | 1103 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 596 | 598 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 686 | 689 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 747 | 750 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 605 | 609 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 646 | 650 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 662 | 667 | PF00026 | 0.255 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L8 | Leptomonas seymouri | 49% | 100% |
A0A0S4IUZ2 | Bodo saltans | 30% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 29% | 100% |
A0A3S5H4W3 | Leishmania donovani | 69% | 100% |
A4HRI7 | Leishmania infantum | 69% | 100% |
C9ZXL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AC55 | Leishmania major | 69% | 100% |
E9AJF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |