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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 11 |
GO:0005737 | cytoplasm | 2 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0140535 | intracellular protein-containing complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1990234 | transferase complex | 3 | 11 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7X374
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 11 |
GO:0009057 | macromolecule catabolic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010033 | response to organic substance | 3 | 11 |
GO:0010243 | response to organonitrogen compound | 4 | 11 |
GO:0010498 | proteasomal protein catabolic process | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 11 |
GO:0030163 | protein catabolic process | 4 | 11 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 11 |
GO:0036503 | ERAD pathway | 5 | 11 |
GO:0042221 | response to chemical | 2 | 11 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044248 | cellular catabolic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 11 |
GO:1901575 | organic substance catabolic process | 3 | 11 |
GO:1901698 | response to nitrogen compound | 3 | 11 |
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 11 |
GO:0034450 | ubiquitin-ubiquitin ligase activity | 6 | 11 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 11 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 757 | 761 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 772 | 776 | PF00656 | 0.407 |
CLV_NRD_NRD_1 | 1006 | 1008 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 867 | 869 | PF00675 | 0.272 |
CLV_PCSK_KEX2_1 | 1006 | 1008 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 867 | 869 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 995 | 997 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.188 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 838 | 842 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 870 | 874 | PF00082 | 0.272 |
CLV_Separin_Metazoa | 670 | 674 | PF03568 | 0.536 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.318 |
DEG_APCC_DBOX_1 | 852 | 860 | PF00400 | 0.490 |
DEG_Kelch_Keap1_1 | 735 | 740 | PF01344 | 0.429 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.330 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.417 |
DOC_CKS1_1 | 940 | 945 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 233 | 241 | PF00134 | 0.396 |
DOC_CYCLIN_RxL_1 | 348 | 359 | PF00134 | 0.336 |
DOC_CYCLIN_RxL_1 | 502 | 509 | PF00134 | 0.536 |
DOC_CYCLIN_yCln2_LP_2 | 173 | 179 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 944 | 950 | PF00134 | 0.517 |
DOC_MAPK_gen_1 | 165 | 174 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 851 | 859 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 49 | 55 | PF00149 | 0.348 |
DOC_PP1_RVXF_1 | 519 | 525 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.348 |
DOC_PP4_FxxP_1 | 594 | 597 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 832 | 835 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 774 | 778 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 913 | 917 | PF00917 | 0.612 |
DOC_USP7_UBL2_3 | 592 | 596 | PF12436 | 0.548 |
DOC_USP7_UBL2_3 | 660 | 664 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 939 | 944 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 247 | 256 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 468 | 473 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 565 | 570 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 687 | 693 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 783 | 788 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 896 | 905 | PF00244 | 0.568 |
LIG_APCC_ABBA_1 | 798 | 803 | PF00400 | 0.548 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.345 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.319 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.259 |
LIG_BRCT_BRCA1_1 | 804 | 808 | PF00533 | 0.514 |
LIG_BRCT_BRCA1_1 | 868 | 872 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_2 | 804 | 810 | PF00533 | 0.514 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.320 |
LIG_deltaCOP1_diTrp_1 | 295 | 303 | PF00928 | 0.276 |
LIG_eIF4E_1 | 554 | 560 | PF01652 | 0.458 |
LIG_eIF4E_1 | 934 | 940 | PF01652 | 0.615 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.367 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.458 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.458 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.514 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.314 |
LIG_FHA_1 | 940 | 946 | PF00498 | 0.542 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.348 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.385 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.387 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.458 |
LIG_FHA_2 | 777 | 783 | PF00498 | 0.587 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.348 |
LIG_FHA_2 | 890 | 896 | PF00498 | 0.494 |
LIG_GBD_Chelix_1 | 231 | 239 | PF00786 | 0.593 |
LIG_GBD_Chelix_1 | 528 | 536 | PF00786 | 0.258 |
LIG_GBD_Chelix_1 | 817 | 825 | PF00786 | 0.258 |
LIG_LIR_Apic_2 | 28 | 32 | PF02991 | 0.258 |
LIG_LIR_Apic_2 | 591 | 597 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 158 | 169 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 636 | 646 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 686 | 696 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 76 | 82 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 799 | 809 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 407 | 411 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 551 | 555 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 636 | 641 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 644 | 649 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 799 | 804 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 861 | 866 | PF02991 | 0.538 |
LIG_MLH1_MIPbox_1 | 254 | 258 | PF16413 | 0.408 |
LIG_MLH1_MIPbox_1 | 371 | 375 | PF16413 | 0.272 |
LIG_MYND_1 | 943 | 947 | PF01753 | 0.541 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.385 |
LIG_NRBOX | 507 | 513 | PF00104 | 0.525 |
LIG_NRBOX | 6 | 12 | PF00104 | 0.332 |
LIG_NRBOX | 935 | 941 | PF00104 | 0.561 |
LIG_NRBOX | 967 | 973 | PF00104 | 0.582 |
LIG_PCNA_PIPBox_1 | 569 | 578 | PF02747 | 0.543 |
LIG_PCNA_TLS_4 | 632 | 639 | PF02747 | 0.548 |
LIG_PCNA_yPIPBox_3 | 557 | 565 | PF02747 | 0.548 |
LIG_PCNA_yPIPBox_3 | 697 | 709 | PF02747 | 0.514 |
LIG_PCNA_yPIPBox_3 | 965 | 977 | PF02747 | 0.637 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.258 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.434 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.377 |
LIG_PTB_Apo_2 | 587 | 594 | PF02174 | 0.458 |
LIG_PTB_Phospho_1 | 587 | 593 | PF10480 | 0.458 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.417 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.421 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 962 | 965 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 646 | 650 | PF00017 | 0.451 |
LIG_SH2_PTP2 | 638 | 641 | PF00017 | 0.458 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 653 | 657 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 934 | 938 | PF00017 | 0.593 |
LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 554 | 557 | PF00017 | 0.458 |
LIG_SH2_STAT3 | 962 | 965 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 962 | 965 | PF00017 | 0.510 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.370 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.273 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.275 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.515 |
LIG_SH3_3 | 945 | 951 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 17 | 24 | PF11976 | 0.314 |
LIG_SUMO_SIM_anti_2 | 582 | 587 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 17 | 24 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 298 | 304 | PF11976 | 0.297 |
LIG_SxIP_EBH_1 | 68 | 80 | PF03271 | 0.348 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.518 |
LIG_TRFH_1 | 279 | 283 | PF08558 | 0.348 |
LIG_UBA3_1 | 138 | 145 | PF00899 | 0.419 |
LIG_UBA3_1 | 278 | 284 | PF00899 | 0.348 |
LIG_UBA3_1 | 583 | 592 | PF00899 | 0.548 |
LIG_WRC_WIRS_1 | 427 | 432 | PF05994 | 0.314 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.540 |
LIG_WRC_WIRS_1 | 74 | 79 | PF05994 | 0.290 |
LIG_WRPW_2 | 456 | 459 | PF00400 | 0.342 |
MOD_CDC14_SPxK_1 | 304 | 307 | PF00782 | 0.297 |
MOD_CDK_SPxK_1 | 301 | 307 | PF00069 | 0.297 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.329 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.396 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.497 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.514 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.482 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.388 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.352 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.543 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.458 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.463 |
MOD_CK2_1 | 734 | 740 | PF00069 | 0.554 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.350 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.566 |
MOD_Cter_Amidation | 1004 | 1007 | PF01082 | 0.408 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.703 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.604 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.540 |
MOD_GlcNHglycan | 516 | 520 | PF01048 | 0.334 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.276 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.452 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.455 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.348 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.410 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.409 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.313 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.341 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.348 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.543 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.573 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.348 |
MOD_GSK3_1 | 877 | 884 | PF00069 | 0.543 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.465 |
MOD_LATS_1 | 781 | 787 | PF00433 | 0.548 |
MOD_N-GLC_1 | 680 | 685 | PF02516 | 0.348 |
MOD_N-GLC_1 | 751 | 756 | PF02516 | 0.311 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.365 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.328 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.358 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.355 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.263 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.510 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.458 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.520 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.479 |
MOD_NEK2_1 | 825 | 830 | PF00069 | 0.458 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.504 |
MOD_NEK2_1 | 973 | 978 | PF00069 | 0.595 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.258 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.528 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.421 |
MOD_PIKK_1 | 675 | 681 | PF00454 | 0.543 |
MOD_PIKK_1 | 774 | 780 | PF00454 | 0.548 |
MOD_PIKK_1 | 810 | 816 | PF00454 | 0.498 |
MOD_PK_1 | 123 | 129 | PF00069 | 0.425 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.425 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.567 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.548 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.458 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.549 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.543 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.370 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.405 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.341 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.218 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.348 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.458 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.458 |
MOD_Plk_1 | 680 | 686 | PF00069 | 0.548 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.494 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.338 |
MOD_Plk_2-3 | 642 | 648 | PF00069 | 0.458 |
MOD_Plk_2-3 | 983 | 989 | PF00069 | 0.658 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.313 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.383 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.307 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.311 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.361 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.263 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.342 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.472 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.463 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.290 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.383 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.396 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.297 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.348 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.557 |
MOD_ProDKin_1 | 939 | 945 | PF00069 | 0.539 |
MOD_SUMO_rev_2 | 1015 | 1020 | PF00179 | 0.675 |
MOD_SUMO_rev_2 | 974 | 979 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 983 | 991 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 205 | 210 | PF01217 | 0.314 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 940 | 945 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 747 | 750 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 850 | 853 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 866 | 868 | PF00400 | 0.407 |
TRG_NES_CRM1_1 | 3 | 15 | PF08389 | 0.269 |
TRG_NES_CRM1_1 | 321 | 334 | PF08389 | 0.275 |
TRG_NES_CRM1_1 | 523 | 537 | PF08389 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 505 | 509 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 838 | 843 | PF00026 | 0.348 |
TRG_Pf-PMV_PEXEL_1 | 891 | 895 | PF00026 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 896 | 901 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I203 | Leptomonas seymouri | 76% | 100% |
A0A1X0P3H7 | Trypanosomatidae | 45% | 100% |
A0A3R7KSQ3 | Trypanosoma rangeli | 46% | 100% |
A4HI56 | Leishmania braziliensis | 88% | 100% |
A4I5D2 | Leishmania infantum | 100% | 100% |
C9ZQR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9B0N0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q7K2 | Leishmania major | 96% | 100% |
V5DQS1 | Trypanosoma cruzi | 45% | 100% |