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 | yes | yes: 4, no: 7 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9ASP0
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 12 |
GO:0006505 | GPI anchor metabolic process | 6 | 12 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 12 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006643 | membrane lipid metabolic process | 4 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 12 |
GO:0006664 | glycolipid metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0008654 | phospholipid biosynthetic process | 5 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009247 | glycolipid biosynthetic process | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 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:0045017 | glycerolipid biosynthetic process | 4 | 12 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:1903509 | liposaccharide metabolic process | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000026 | alpha-1,2-mannosyltransferase activity | 6 | 12 |
GO:0000030 | mannosyltransferase activity | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004376 | glycolipid mannosyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016757 | glycosyltransferase activity | 3 | 12 |
GO:0016758 | hexosyltransferase activity | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.382 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.182 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.504 |
DEG_APCC_DBOX_1 | 497 | 505 | PF00400 | 0.272 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.473 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.433 |
DOC_CDC14_PxL_1 | 360 | 368 | PF14671 | 0.286 |
DOC_CDC14_PxL_1 | 381 | 389 | PF14671 | 0.321 |
DOC_CKS1_1 | 271 | 276 | PF01111 | 0.256 |
DOC_CYCLIN_RxL_1 | 234 | 244 | PF00134 | 0.387 |
DOC_CYCLIN_RxL_1 | 265 | 273 | PF00134 | 0.180 |
DOC_CYCLIN_RxL_1 | 425 | 434 | PF00134 | 0.516 |
DOC_MAPK_DCC_7 | 378 | 388 | PF00069 | 0.265 |
DOC_MAPK_gen_1 | 413 | 421 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 527 | 537 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 27 | 34 | PF00069 | 0.283 |
DOC_MAPK_NFAT4_5 | 27 | 35 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 237 | 244 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 266 | 273 | PF00149 | 0.259 |
DOC_PP1_RVXF_1 | 376 | 383 | PF00149 | 0.323 |
DOC_PP1_RVXF_1 | 489 | 495 | PF00149 | 0.343 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.323 |
DOC_PP4_FxxP_1 | 587 | 590 | PF00568 | 0.178 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.140 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.232 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.238 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.266 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.235 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 428 | 434 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.149 |
LIG_14-3-3_CanoR_1 | 514 | 523 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.316 |
LIG_Actin_WH2_2 | 21 | 37 | PF00022 | 0.193 |
LIG_Actin_WH2_2 | 391 | 409 | PF00022 | 0.275 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.300 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.265 |
LIG_CSL_BTD_1 | 314 | 317 | PF09270 | 0.376 |
LIG_eIF4E_1 | 381 | 387 | PF01652 | 0.376 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.367 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.228 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.223 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.421 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.376 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.358 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.465 |
LIG_IRF3_LxIS_1 | 384 | 391 | PF10401 | 0.275 |
LIG_LIR_Apic_2 | 136 | 141 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 584 | 590 | PF02991 | 0.184 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.216 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 376 | 387 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 479 | 489 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 610 | 620 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.191 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.285 |
LIG_MLH1_MIPbox_1 | 186 | 190 | PF16413 | 0.300 |
LIG_NRBOX | 18 | 24 | PF00104 | 0.370 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.243 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.382 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.419 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.382 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.413 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.268 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.316 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.316 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.238 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.316 |
LIG_SH2_CRK | 600 | 604 | PF00017 | 0.277 |
LIG_SH2_GRB2like | 181 | 184 | PF00017 | 0.286 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.316 |
LIG_SH2_PTP2 | 71 | 74 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.321 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.234 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.288 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.244 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.425 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.245 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.402 |
LIG_SUMO_SIM_anti_2 | 161 | 168 | PF11976 | 0.205 |
LIG_SUMO_SIM_anti_2 | 391 | 398 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.275 |
LIG_SUMO_SIM_par_1 | 385 | 392 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 533 | 539 | PF11976 | 0.239 |
LIG_TRAF2_1 | 605 | 608 | PF00917 | 0.322 |
LIG_TRFH_1 | 381 | 385 | PF08558 | 0.376 |
LIG_TYR_ITIM | 265 | 270 | PF00017 | 0.260 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.214 |
LIG_UBA3_1 | 261 | 268 | PF00899 | 0.403 |
LIG_UBA3_1 | 283 | 288 | PF00899 | 0.207 |
LIG_UBA3_1 | 81 | 85 | PF00899 | 0.436 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.228 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.444 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.140 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.127 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.479 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.518 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.300 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.363 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.421 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.559 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.226 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.450 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.252 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.212 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.399 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.319 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.341 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.326 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.171 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.332 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.301 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.499 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.536 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.522 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.509 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.457 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.376 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.260 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.295 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.312 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.540 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.534 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.398 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.376 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.550 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.173 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.523 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.317 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.264 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.244 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.279 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.327 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.279 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.541 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.300 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.352 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.347 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.524 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.293 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.358 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.381 |
MOD_PK_1 | 530 | 536 | PF00069 | 0.222 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.340 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.520 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.235 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.275 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.349 |
MOD_PKB_1 | 411 | 419 | PF00069 | 0.390 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.516 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.552 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.324 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.299 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.263 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.515 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.322 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.354 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.262 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.335 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.428 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.510 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.230 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.238 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.266 |
MOD_SUMO_for_1 | 562 | 565 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 370 | 377 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_1 | 556 | 561 | PF01217 | 0.254 |
TRG_DiLeu_BaEn_2 | 185 | 191 | PF01217 | 0.260 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.275 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.218 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.217 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.256 |
TRG_NLS_MonoExtC_3 | 152 | 157 | PF00514 | 0.382 |
TRG_NLS_MonoExtN_4 | 151 | 157 | PF00514 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 527 | 531 | PF00026 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Q8 | Leptomonas seymouri | 56% | 100% |
A0A0S4J7A7 | Bodo saltans | 29% | 100% |
A0A1X0P926 | Trypanosomatidae | 32% | 100% |
A0A3Q8IJ48 | Leishmania donovani | 83% | 100% |
A0A422NTW3 | Trypanosoma rangeli | 31% | 100% |
A4HNY0 | Leishmania braziliensis | 69% | 100% |
A4ICL4 | Leishmania infantum | 84% | 100% |
D0A2U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
P86935 | Trypanosoma brucei brucei | 33% | 100% |
P86936 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 33% | 100% |
Q1LZA0 | Bos taurus | 26% | 100% |
Q4Q1V6 | Leishmania major | 81% | 100% |
Q4V7R2 | Xenopus laevis | 24% | 100% |
Q6BH65 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 22% | 100% |
Q6CAB8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 100% |
Q6CN76 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 100% |
Q6FTY5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 22% | 100% |
Q75BG9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 100% |
Q7SXZ1 | Danio rerio | 25% | 100% |
Q92521 | Homo sapiens | 24% | 100% |
Q94A15 | Arabidopsis thaliana | 25% | 100% |
Q9JJQ0 | Mus musculus | 25% | 100% |
Q9USN0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q9VZM5 | Drosophila melanogaster | 25% | 100% |
V5DRF7 | Trypanosoma cruzi | 32% | 100% |