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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0005782 | peroxisomal matrix | 6 | 1 |
GO:0031907 | microbody lumen | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H525
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006631 | fatty acid metabolic process | 4 | 12 |
GO:0006633 | fatty acid biosynthetic process | 5 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016053 | organic acid biosynthetic process | 4 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0044283 | small molecule biosynthetic process | 3 | 12 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0006084 | acetyl-CoA metabolic process | 5 | 1 |
GO:0006085 | acetyl-CoA biosynthetic process | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 1 |
GO:0006195 | purine nucleotide catabolic process | 6 | 1 |
GO:0006637 | acyl-CoA metabolic process | 4 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006790 | sulfur compound metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 1 |
GO:0009154 | purine ribonucleotide catabolic process | 6 | 1 |
GO:0009165 | nucleotide biosynthetic process | 6 | 1 |
GO:0009166 | nucleotide catabolic process | 6 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 1 |
GO:0009261 | ribonucleotide catabolic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010565 | regulation of cellular ketone metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019216 | regulation of lipid metabolic process | 5 | 1 |
GO:0019217 | regulation of fatty acid metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0033865 | nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0033866 | nucleoside bisphosphate biosynthetic process | 6 | 1 |
GO:0033869 | nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0033875 | ribonucleoside bisphosphate metabolic process | 6 | 1 |
GO:0034030 | ribonucleoside bisphosphate biosynthetic process | 7 | 1 |
GO:0034031 | ribonucleoside bisphosphate catabolic process | 7 | 1 |
GO:0034032 | purine nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0034033 | purine nucleoside bisphosphate biosynthetic process | 6 | 1 |
GO:0034034 | purine nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0035383 | thioester metabolic process | 3 | 1 |
GO:0035384 | thioester biosynthetic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 1 |
GO:0044273 | sulfur compound catabolic process | 4 | 1 |
GO:0045834 | positive regulation of lipid metabolic process | 5 | 1 |
GO:0045923 | positive regulation of fatty acid metabolic process | 6 | 1 |
GO:0046320 | regulation of fatty acid oxidation | 7 | 1 |
GO:0046321 | positive regulation of fatty acid oxidation | 7 | 1 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0062012 | regulation of small molecule metabolic process | 4 | 1 |
GO:0062013 | positive regulation of small molecule metabolic process | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071616 | acyl-CoA biosynthetic process | 5 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 1 |
GO:0072523 | purine-containing compound catabolic process | 5 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 1 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:2001293 | malonyl-CoA metabolic process | 5 | 1 |
GO:2001294 | malonyl-CoA catabolic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016829 | lyase activity | 2 | 12 |
GO:0016830 | carbon-carbon lyase activity | 3 | 12 |
GO:0016831 | carboxy-lyase activity | 4 | 12 |
GO:0050080 | malonyl-CoA decarboxylase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.316 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 178 | 180 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.505 |
CLV_Separin_Metazoa | 476 | 480 | PF03568 | 0.341 |
DEG_SCF_FBW7_1 | 417 | 422 | PF00400 | 0.535 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.419 |
DEG_SPOP_SBC_1 | 355 | 359 | PF00917 | 0.474 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.535 |
DOC_CKS1_1 | 567 | 572 | PF01111 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 338 | 344 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 38 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 651 | 657 | PF00134 | 0.374 |
DOC_MAPK_gen_1 | 226 | 236 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.397 |
DOC_PP1_RVXF_1 | 605 | 611 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.538 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.497 |
DOC_PP2B_PxIxI_1 | 311 | 317 | PF00149 | 0.442 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.471 |
DOC_USP7_UBL2_3 | 178 | 182 | PF12436 | 0.444 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 167 | 176 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 573 | 579 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 647 | 652 | PF00244 | 0.257 |
LIG_Actin_WH2_2 | 560 | 575 | PF00022 | 0.391 |
LIG_Actin_WH2_2 | 78 | 95 | PF00022 | 0.408 |
LIG_AP2alpha_1 | 245 | 249 | PF02296 | 0.252 |
LIG_APCC_ABBAyCdc20_2 | 10 | 16 | PF00400 | 0.336 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.312 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.490 |
LIG_CtBP_PxDLS_1 | 389 | 395 | PF00389 | 0.478 |
LIG_deltaCOP1_diTrp_1 | 26 | 32 | PF00928 | 0.463 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.442 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.498 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.390 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.442 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.369 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.615 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.540 |
LIG_IRF3_LxIS_1 | 57 | 62 | PF10401 | 0.225 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 26 | 37 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 422 | 431 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 472 | 478 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.406 |
LIG_NRBOX | 521 | 527 | PF00104 | 0.453 |
LIG_PCNA_yPIPBox_3 | 388 | 401 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 508 | 522 | PF02747 | 0.403 |
LIG_PCNA_yPIPBox_3 | 68 | 80 | PF02747 | 0.361 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.246 |
LIG_PTB_Apo_2 | 625 | 632 | PF02174 | 0.431 |
LIG_PTB_Phospho_1 | 625 | 631 | PF10480 | 0.431 |
LIG_REV1ctd_RIR_1 | 246 | 255 | PF16727 | 0.262 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.490 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.546 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.465 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.565 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.442 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 86 | 93 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 646 | 653 | PF11976 | 0.296 |
LIG_SxIP_EBH_1 | 422 | 434 | PF03271 | 0.462 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.461 |
LIG_TYR_ITIM | 145 | 150 | PF00017 | 0.362 |
LIG_WRC_WIRS_1 | 420 | 425 | PF05994 | 0.281 |
LIG_WW_3 | 187 | 191 | PF00397 | 0.459 |
MOD_CDK_SPxxK_3 | 545 | 552 | PF00069 | 0.478 |
MOD_CDK_SPxxK_3 | 566 | 573 | PF00069 | 0.210 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.621 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.491 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.304 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.281 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.584 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.744 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.331 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.266 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.668 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.511 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.493 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.607 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.503 |
MOD_CK2_1 | 647 | 653 | PF00069 | 0.394 |
MOD_DYRK1A_RPxSP_1 | 415 | 419 | PF00069 | 0.411 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.595 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.659 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.329 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.427 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.574 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.379 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.340 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.671 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.659 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.283 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.502 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.543 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.268 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.326 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.272 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.590 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.692 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.331 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.287 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.300 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.276 |
MOD_LATS_1 | 165 | 171 | PF00433 | 0.377 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.357 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.411 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.467 |
MOD_N-GLC_1 | 612 | 617 | PF02516 | 0.266 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.377 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.493 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.329 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.210 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.314 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.449 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.281 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.411 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.189 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.364 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.563 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.463 |
MOD_PK_1 | 274 | 280 | PF00069 | 0.331 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.374 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.402 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.281 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.260 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.602 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.281 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.401 |
MOD_Plk_1 | 559 | 565 | PF00069 | 0.265 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.479 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.469 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.437 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.350 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.322 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.331 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.281 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.401 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.364 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.370 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.625 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.267 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.281 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.287 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.241 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.335 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.628 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.414 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 127 | 130 | PF00179 | 0.396 |
TRG_DiLeu_BaEn_1 | 120 | 125 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_2 | 53 | 59 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 309 | 314 | PF01217 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 567 | 572 | PF01217 | 0.281 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF8 | Leptomonas seymouri | 59% | 84% |
A0A0S4J4K1 | Bodo saltans | 30% | 100% |
A0A1X0NPQ8 | Trypanosomatidae | 41% | 86% |
A0A3R7N686 | Trypanosoma rangeli | 42% | 92% |
A0A3S5H5Z5 | Leishmania donovani | 78% | 83% |
A4HT98 | Leishmania infantum | 78% | 83% |
C9ZUM4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 90% |
E9AL87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 83% |
Q4QIL8 | Leishmania major | 77% | 100% |
V5BY47 | Trypanosoma cruzi | 44% | 100% |