Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 2 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 5 |
Forrest at al. (procyclic) | no | yes: 5 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 29 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 27 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 5, no: 41 |
NetGPI | no | yes: 0, no: 46 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 46 |
GO:0110165 | cellular anatomical entity | 1 | 47 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0016020 | membrane | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 9 |
GO:0005739 | mitochondrion | 5 | 4 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005788 | endoplasmic reticulum lumen | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034663 | endoplasmic reticulum chaperone complex | 3 | 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: A4HEU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 9 |
GO:0006458 | 'de novo' protein folding | 3 | 9 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006986 | response to unfolded protein | 4 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0010033 | response to organic substance | 3 | 9 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034620 | cellular response to unfolded protein | 5 | 9 |
GO:0035966 | response to topologically incorrect protein | 3 | 9 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 9 |
GO:0042026 | protein refolding | 3 | 9 |
GO:0042221 | response to chemical | 2 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 9 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0061077 | chaperone-mediated protein folding | 3 | 9 |
GO:0070887 | cellular response to chemical stimulus | 3 | 9 |
GO:0071310 | cellular response to organic substance | 4 | 9 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 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: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:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 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:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0065007 | biological regulation | 1 | 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 | 47 |
GO:0005488 | binding | 1 | 47 |
GO:0005524 | ATP binding | 5 | 47 |
GO:0017076 | purine nucleotide binding | 4 | 47 |
GO:0030554 | adenyl nucleotide binding | 5 | 47 |
GO:0032553 | ribonucleotide binding | 3 | 47 |
GO:0032555 | purine ribonucleotide binding | 4 | 47 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 47 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 47 |
GO:0036094 | small molecule binding | 2 | 47 |
GO:0043167 | ion binding | 2 | 47 |
GO:0043168 | anion binding | 3 | 47 |
GO:0044183 | protein folding chaperone | 1 | 47 |
GO:0097159 | organic cyclic compound binding | 2 | 47 |
GO:0097367 | carbohydrate derivative binding | 2 | 47 |
GO:0140657 | ATP-dependent activity | 1 | 47 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 47 |
GO:1901265 | nucleoside phosphate binding | 3 | 47 |
GO:1901363 | heterocyclic compound binding | 2 | 47 |
GO:0005515 | protein binding | 2 | 21 |
GO:0051082 | unfolded protein binding | 3 | 21 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0016887 | ATP hydrolysis activity | 7 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
GO:0031072 | heat shock protein binding | 3 | 9 |
GO:0051787 | misfolded protein binding | 3 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 682 | 686 | PF00656 | 0.480 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 769 | 771 | PF00675 | 0.539 |
CLV_PCSK_FUR_1 | 276 | 280 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 881 | 883 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 644 | 646 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 881 | 883 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 279 | 285 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 861 | 865 | PF00082 | 0.451 |
CLV_Separin_Metazoa | 669 | 673 | PF03568 | 0.399 |
DEG_SCF_FBW7_1 | 287 | 293 | PF00400 | 0.459 |
DOC_CKS1_1 | 234 | 239 | PF01111 | 0.232 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.456 |
DOC_CYCLIN_RxL_1 | 327 | 336 | PF00134 | 0.233 |
DOC_CYCLIN_RxL_1 | 404 | 414 | PF00134 | 0.232 |
DOC_CYCLIN_RxL_1 | 495 | 505 | PF00134 | 0.314 |
DOC_CYCLIN_RxL_1 | 563 | 575 | PF00134 | 0.460 |
DOC_CYCLIN_RxL_1 | 610 | 621 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 458 | 464 | PF00134 | 0.247 |
DOC_CYCLIN_yCln2_LP_2 | 851 | 857 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 439 | 446 | PF00069 | 0.244 |
DOC_MAPK_gen_1 | 563 | 571 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 187 | 194 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.232 |
DOC_PP1_RVXF_1 | 415 | 421 | PF00149 | 0.232 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.228 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 775 | 779 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 802 | 806 | PF00917 | 0.566 |
DOC_USP7_MATH_2 | 823 | 829 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 721 | 725 | PF12436 | 0.654 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.543 |
LIG_14-3-3_CanoR_1 | 148 | 155 | PF00244 | 0.235 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 803 | 807 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 853 | 858 | PF00244 | 0.455 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.232 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.235 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.234 |
LIG_BRCT_BRCA1_2 | 376 | 382 | PF00533 | 0.314 |
LIG_Clathr_ClatBox_1 | 604 | 608 | PF01394 | 0.431 |
LIG_EH1_1 | 198 | 206 | PF00400 | 0.232 |
LIG_EH1_1 | 251 | 259 | PF00400 | 0.304 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.232 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.232 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.337 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.488 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.674 |
LIG_FHA_1 | 888 | 894 | PF00498 | 0.538 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.306 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.275 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.371 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.232 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.245 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.386 |
LIG_FHA_2 | 715 | 721 | PF00498 | 0.629 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.632 |
LIG_FHA_2 | 854 | 860 | PF00498 | 0.453 |
LIG_FHA_2 | 890 | 896 | PF00498 | 0.600 |
LIG_GBD_Chelix_1 | 201 | 209 | PF00786 | 0.244 |
LIG_GBD_Chelix_1 | 673 | 681 | PF00786 | 0.551 |
LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 385 | 391 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 813 | 819 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 371 | 380 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 453 | 462 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 828 | 836 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 828 | 832 | PF02991 | 0.409 |
LIG_LRP6_Inhibitor_1 | 576 | 588 | PF00058 | 0.480 |
LIG_MAD2 | 510 | 518 | PF02301 | 0.229 |
LIG_NRP_CendR_1 | 935 | 938 | PF00754 | 0.554 |
LIG_PCNA_TLS_4 | 500 | 507 | PF02747 | 0.229 |
LIG_Pex14_2 | 380 | 384 | PF04695 | 0.297 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.244 |
LIG_SH2_GRB2like | 52 | 55 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 430 | 434 | PF00017 | 0.232 |
LIG_SH2_PTP2 | 455 | 458 | PF00017 | 0.221 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.304 |
LIG_SH2_SRC | 322 | 325 | PF00017 | 0.200 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 600 | 604 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.562 |
LIG_SH3_2 | 43 | 48 | PF14604 | 0.538 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.368 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.434 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.550 |
LIG_SH3_3 | 737 | 743 | PF00018 | 0.595 |
LIG_SH3_3 | 758 | 764 | PF00018 | 0.507 |
LIG_SH3_3 | 816 | 822 | PF00018 | 0.530 |
LIG_SH3_3 | 839 | 845 | PF00018 | 0.461 |
LIG_SH3_3 | 867 | 873 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 253 | 260 | PF11976 | 0.236 |
LIG_SUMO_SIM_anti_2 | 485 | 491 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 179 | 186 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 253 | 260 | PF11976 | 0.232 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.314 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.248 |
LIG_TRAF2_1 | 593 | 596 | PF00917 | 0.452 |
LIG_UBA3_1 | 561 | 570 | PF00899 | 0.421 |
LIG_UBA3_1 | 646 | 654 | PF00899 | 0.457 |
LIG_UBA3_1 | 857 | 861 | PF00899 | 0.445 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.232 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.487 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.253 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.439 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.247 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.306 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.486 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.432 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.493 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.670 |
MOD_CK2_1 | 825 | 831 | PF00069 | 0.458 |
MOD_CK2_1 | 853 | 859 | PF00069 | 0.461 |
MOD_CK2_1 | 889 | 895 | PF00069 | 0.605 |
MOD_Cter_Amidation | 157 | 160 | PF01082 | 0.344 |
MOD_Cter_Amidation | 507 | 510 | PF01082 | 0.314 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.257 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.264 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.505 |
MOD_GlcNHglycan | 259 | 264 | PF01048 | 0.252 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.606 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.515 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.529 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.522 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.617 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.657 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.762 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.553 |
MOD_GlcNHglycan | 800 | 803 | PF01048 | 0.620 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.536 |
MOD_GlcNHglycan | 874 | 877 | PF01048 | 0.502 |
MOD_GlcNHglycan | 931 | 935 | PF01048 | 0.440 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.247 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.521 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.306 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.265 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.544 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.559 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.543 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.625 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.429 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.477 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.490 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.573 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.587 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.522 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.545 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.200 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.232 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.543 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.278 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.239 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.232 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.279 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.351 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.270 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.419 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.496 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.556 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.639 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.623 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.372 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.232 |
MOD_PIKK_1 | 701 | 707 | PF00454 | 0.480 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.575 |
MOD_PKA_1 | 283 | 289 | PF00069 | 0.488 |
MOD_PKA_1 | 629 | 635 | PF00069 | 0.486 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.465 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.234 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.495 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.487 |
MOD_PKA_2 | 802 | 808 | PF00069 | 0.498 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.432 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.200 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.269 |
MOD_Plk_2-3 | 825 | 831 | PF00069 | 0.441 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.347 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.325 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.285 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.473 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.341 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.354 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.498 |
MOD_Plk_4 | 853 | 859 | PF00069 | 0.447 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.345 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.486 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.232 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.477 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.542 |
MOD_SUMO_for_1 | 212 | 215 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.379 |
MOD_SUMO_for_1 | 56 | 59 | PF00179 | 0.472 |
MOD_SUMO_for_1 | 918 | 921 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 301 | 307 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 720 | 727 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 744 | 751 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 825 | 835 | PF00179 | 0.423 |
TRG_DiLeu_BaEn_2 | 214 | 220 | PF01217 | 0.244 |
TRG_DiLeu_BaEn_4 | 453 | 459 | PF01217 | 0.247 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 611 | 616 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 628 | 630 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 767 | 770 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 883 | 895 | PF08389 | 0.569 |
TRG_NLS_MonoExtC_3 | 274 | 279 | PF00514 | 0.334 |
TRG_NLS_MonoExtN_4 | 273 | 279 | PF00514 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 331 | 336 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 500 | 504 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 602 | 606 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 613 | 618 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEK8 | Leptomonas seymouri | 77% | 100% |
A0A1X0NSC2 | Trypanosomatidae | 62% | 100% |
A0A3Q8IB80 | Leishmania donovani | 30% | 100% |
A0A3Q8ICR2 | Leishmania donovani | 88% | 99% |
A0A3Q8IEX7 | Leishmania donovani | 27% | 100% |
A0A3Q8IQX0 | Leishmania donovani | 31% | 100% |
A0A3S7WZX1 | Leishmania donovani | 28% | 100% |
A0A3S7X1F5 | Leishmania donovani | 26% | 100% |
A0A3S7X203 | Leishmania donovani | 25% | 100% |
A0A3S7X3K5 | Leishmania donovani | 27% | 100% |
A0A3S7X3M0 | Leishmania donovani | 27% | 100% |
A4HEX9 | Leishmania braziliensis | 26% | 100% |
A4HGG7 | Leishmania braziliensis | 26% | 100% |
A4HGY1 | Leishmania braziliensis | 29% | 100% |
A4HIH8 | Leishmania braziliensis | 27% | 100% |
A4HII0 | Leishmania braziliensis | 27% | 100% |
A4I219 | Leishmania infantum | 89% | 100% |
A4I253 | Leishmania infantum | 27% | 100% |
A4I3J9 | Leishmania infantum | 26% | 100% |
A4I412 | Leishmania infantum | 31% | 100% |
A4I417 | Leishmania infantum | 26% | 100% |
A4I5S4 | Leishmania infantum | 27% | 100% |
A4I5S5 | Leishmania infantum | 27% | 100% |
A4I5S9 | Leishmania infantum | 27% | 100% |
A4I5T0 | Leishmania infantum | 27% | 100% |
C9ZRY8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E9AHH0 | Leishmania infantum | 30% | 100% |
E9AY68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9AYA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AZT9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B099 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B0A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B119 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B121 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B125 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q740 | Leishmania major | 27% | 100% |
Q4Q744 | Leishmania major | 27% | 100% |
Q4Q745 | Leishmania major | 27% | 100% |
Q4Q747 | Leishmania major | 27% | 100% |
Q4Q7Y0 | Leishmania major | 25% | 100% |
Q4Q7Y4 | Leishmania major | 30% | 100% |
Q4Q8E6 | Leishmania major | 26% | 100% |
Q4Q970 | Leishmania major | 28% | 100% |
Q4Q9A4 | Leishmania major | 89% | 100% |
V5BUG8 | Trypanosoma cruzi | 63% | 100% |