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: A0A3Q8IJ48
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_NRD_NRD_1 | 125 | 127 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.581 |
CLV_PCSK_FUR_1 | 410 | 414 | PF00082 | 0.206 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.397 |
CLV_PCSK_PC7_1 | 351 | 357 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.584 |
CLV_Separin_Metazoa | 555 | 559 | PF03568 | 0.264 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.308 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.267 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.510 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.509 |
DOC_CDC14_PxL_1 | 359 | 367 | PF14671 | 0.395 |
DOC_CDC14_PxL_1 | 380 | 388 | PF14671 | 0.453 |
DOC_CDC14_PxL_1 | 76 | 84 | PF14671 | 0.337 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.279 |
DOC_CKS1_1 | 476 | 481 | PF01111 | 0.271 |
DOC_CYCLIN_RxL_1 | 236 | 246 | PF00134 | 0.428 |
DOC_CYCLIN_RxL_1 | 424 | 433 | PF00134 | 0.540 |
DOC_CYCLIN_yClb1_LxF_4 | 266 | 271 | PF00134 | 0.137 |
DOC_CYCLIN_yCln2_LP_2 | 586 | 592 | PF00134 | 0.366 |
DOC_MAPK_DCC_7 | 377 | 387 | PF00069 | 0.265 |
DOC_MAPK_gen_1 | 410 | 420 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 526 | 536 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 593 | 599 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 17 | 25 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 27 | 34 | PF00069 | 0.293 |
DOC_MAPK_NFAT4_5 | 17 | 25 | PF00069 | 0.443 |
DOC_MAPK_NFAT4_5 | 27 | 35 | PF00069 | 0.409 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.357 |
DOC_PP1_RVXF_1 | 375 | 382 | PF00149 | 0.344 |
DOC_PP1_RVXF_1 | 488 | 494 | PF00149 | 0.368 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.503 |
DOC_PP4_FxxP_1 | 381 | 384 | PF00568 | 0.375 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.303 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.193 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 513 | 522 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.340 |
LIG_Actin_WH2_2 | 390 | 408 | PF00022 | 0.376 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.329 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.322 |
LIG_CSL_BTD_1 | 313 | 316 | PF09270 | 0.415 |
LIG_CSL_BTD_1 | 615 | 618 | PF09270 | 0.183 |
LIG_eIF4E_1 | 380 | 386 | PF01652 | 0.415 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.530 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.434 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.406 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.373 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.396 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.376 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.511 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.559 |
LIG_IRF3_LxIS_1 | 383 | 390 | PF10401 | 0.376 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 215 | 226 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 272 | 282 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 375 | 386 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 478 | 488 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 609 | 618 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.210 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.206 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.317 |
LIG_MLH1_MIPbox_1 | 186 | 190 | PF16413 | 0.329 |
LIG_NRBOX | 18 | 24 | PF00104 | 0.411 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.283 |
LIG_Pex14_2 | 310 | 314 | PF04695 | 0.415 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.427 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.398 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.288 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.340 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.340 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.251 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.279 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 181 | 184 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.340 |
LIG_SH2_PTP2 | 71 | 74 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.374 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.275 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.296 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.245 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.248 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.446 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 390 | 396 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 441 | 446 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 363 | 370 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 384 | 391 | PF11976 | 0.393 |
LIG_TRAF2_1 | 604 | 607 | PF00917 | 0.383 |
LIG_TRFH_1 | 380 | 384 | PF08558 | 0.412 |
LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.298 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.254 |
LIG_UBA3_1 | 556 | 562 | PF00899 | 0.272 |
LIG_UBA3_1 | 81 | 85 | PF00899 | 0.453 |
LIG_WRC_WIRS_1 | 602 | 607 | PF05994 | 0.328 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.551 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.478 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.538 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.555 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.486 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.562 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.257 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.342 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.420 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.335 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.264 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.426 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.341 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.350 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.344 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.229 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.341 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.598 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.515 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.492 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.254 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.215 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.376 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.553 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.424 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.423 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.446 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.415 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.530 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.396 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.185 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.289 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.320 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.336 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.513 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.546 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.354 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.361 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.381 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.495 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.331 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.309 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.375 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.549 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.395 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.406 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.542 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.289 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.376 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.562 |
MOD_PKB_1 | 410 | 418 | PF00069 | 0.434 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.540 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.372 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.307 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.559 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.346 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.384 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.324 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.519 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.483 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.254 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.279 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.276 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.207 |
MOD_SUMO_for_1 | 561 | 564 | PF00179 | 0.332 |
MOD_SUMO_rev_2 | 369 | 376 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_2 | 185 | 191 | PF01217 | 0.298 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.223 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.368 |
TRG_NES_CRM1_1 | 489 | 501 | PF08389 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Q8 | Leptomonas seymouri | 56% | 100% |
A0A0S4J7A7 | Bodo saltans | 28% | 100% |
A0A1X0P926 | Trypanosomatidae | 33% | 100% |
A0A422NTW3 | Trypanosoma rangeli | 32% | 100% |
A4HNY0 | Leishmania braziliensis | 70% | 100% |
A4ICL4 | Leishmania infantum | 99% | 100% |
D0A2U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ASP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
P30777 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
P86935 | Trypanosoma brucei brucei | 34% | 100% |
P86936 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 34% | 100% |
Q4Q1V6 | Leishmania major | 88% | 100% |
Q4V7R2 | Xenopus laevis | 24% | 100% |
Q6CN76 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 22% | 100% |
Q6FTY5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 100% |
Q7SXZ1 | Danio rerio | 25% | 100% |
Q94A15 | Arabidopsis thaliana | 25% | 100% |
Q9JJQ0 | Mus musculus | 25% | 100% |
Q9USN0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q9VZM5 | Drosophila melanogaster | 27% | 100% |
V5DRF7 | Trypanosoma cruzi | 32% | 100% |