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: 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: A4HNY0
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 | 233 | 235 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.428 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.157 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.404 |
CLV_PCSK_PC7_1 | 352 | 358 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.530 |
DEG_MDM2_SWIB_1 | 431 | 439 | PF02201 | 0.170 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.583 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.408 |
DOC_CDC14_PxL_1 | 381 | 389 | PF14671 | 0.322 |
DOC_CKS1_1 | 271 | 276 | PF01111 | 0.256 |
DOC_CKS1_1 | 477 | 482 | PF01111 | 0.265 |
DOC_CKS1_1 | 600 | 605 | PF01111 | 0.246 |
DOC_CYCLIN_RxL_1 | 425 | 432 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 521 | 533 | PF00134 | 0.241 |
DOC_CYCLIN_yCln2_LP_2 | 560 | 566 | PF00134 | 0.234 |
DOC_CYCLIN_yCln2_LP_2 | 587 | 593 | PF00134 | 0.350 |
DOC_MAPK_DCC_7 | 239 | 249 | PF00069 | 0.357 |
DOC_MAPK_DCC_7 | 378 | 388 | PF00069 | 0.225 |
DOC_MAPK_gen_1 | 12 | 22 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 276 | 286 | PF00069 | 0.157 |
DOC_MAPK_gen_1 | 356 | 363 | PF00069 | 0.219 |
DOC_MAPK_gen_1 | 527 | 537 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 15 | 24 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 27 | 34 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 356 | 363 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 500 | 507 | PF00069 | 0.256 |
DOC_MAPK_NFAT4_5 | 27 | 35 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 221 | 235 | PF00069 | 0.170 |
DOC_MAPK_RevD_3 | 308 | 322 | PF00069 | 0.159 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.265 |
DOC_PP1_RVXF_1 | 274 | 281 | PF00149 | 0.215 |
DOC_PP1_RVXF_1 | 376 | 383 | PF00149 | 0.324 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 529 | 532 | PF13499 | 0.218 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.324 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.251 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.233 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 546 | 550 | PF12436 | 0.391 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.231 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.222 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 198 | 202 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.235 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 416 | 420 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 428 | 434 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.317 |
LIG_Actin_RPEL_3 | 371 | 390 | PF02755 | 0.279 |
LIG_Actin_WH2_2 | 110 | 127 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 21 | 37 | PF00022 | 0.194 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.300 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.159 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.265 |
LIG_deltaCOP1_diTrp_1 | 462 | 467 | PF00928 | 0.195 |
LIG_deltaCOP1_diTrp_1 | 63 | 67 | PF00928 | 0.157 |
LIG_eIF4E_1 | 337 | 343 | PF01652 | 0.357 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.404 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.229 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.447 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.350 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.217 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.330 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.465 |
LIG_GBD_Chelix_1 | 184 | 192 | PF00786 | 0.435 |
LIG_LIR_Apic_2 | 474 | 480 | PF02991 | 0.229 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 376 | 387 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 414 | 425 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 479 | 489 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 48 | 55 | PF02991 | 0.184 |
LIG_LIR_Gen_1 | 61 | 72 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 610 | 621 | PF02991 | 0.339 |
LIG_LIR_LC3C_4 | 418 | 421 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.285 |
LIG_MLH1_MIPbox_1 | 186 | 190 | PF16413 | 0.300 |
LIG_MLH1_MIPbox_1 | 286 | 290 | PF16413 | 0.176 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.243 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.364 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.382 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.420 |
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 | 0.317 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.317 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.212 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.239 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.306 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.170 |
LIG_SH2_GRB2like | 181 | 184 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 369 | 373 | PF00017 | 0.182 |
LIG_SH2_NCK_1 | 477 | 481 | PF00017 | 0.158 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.176 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.176 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.340 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.170 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.235 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.288 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.271 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.170 |
LIG_SUMO_SIM_anti_2 | 391 | 397 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 442 | 447 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 490 | 496 | PF11976 | 0.200 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 245 | 250 | PF11976 | 0.219 |
LIG_SUMO_SIM_par_1 | 385 | 392 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 394 | 402 | PF11976 | 0.351 |
LIG_TRFH_1 | 381 | 385 | PF08558 | 0.377 |
LIG_TRFH_1 | 7 | 11 | PF08558 | 0.225 |
LIG_TYR_ITIM | 265 | 270 | PF00017 | 0.315 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.250 |
LIG_UBA3_1 | 367 | 375 | PF00899 | 0.170 |
LIG_UBA3_1 | 81 | 85 | PF00899 | 0.437 |
MOD_CDK_SPxK_1 | 270 | 276 | PF00069 | 0.170 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.350 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.277 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.349 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.376 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.465 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.374 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.180 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.268 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.432 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.306 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.403 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.322 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.413 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.400 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.397 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.416 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.373 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.383 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.232 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.311 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.308 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.441 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.390 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.419 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.324 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.377 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.170 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.194 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.331 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.317 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.320 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.238 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.409 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.279 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.429 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.352 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.347 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.310 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.385 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.170 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.358 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.170 |
MOD_PKA_1 | 546 | 552 | PF00069 | 0.367 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.296 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.235 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.387 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.210 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.394 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.221 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.444 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.237 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.369 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.328 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.460 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.393 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.323 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.355 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.421 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.385 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.310 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.274 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.324 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.284 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.453 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.324 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.261 |
MOD_SUMO_rev_2 | 370 | 377 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 539 | 549 | PF00179 | 0.427 |
TRG_DiLeu_BaEn_2 | 185 | 191 | PF01217 | 0.315 |
TRG_DiLeu_BaEn_2 | 219 | 225 | PF01217 | 0.170 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.170 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.310 |
TRG_NES_CRM1_1 | 484 | 496 | PF08389 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.229 |
TRG_Pf-PMV_PEXEL_1 | 458 | 462 | PF00026 | 0.170 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Q8 | Leptomonas seymouri | 55% | 100% |
A0A0S4J7A7 | Bodo saltans | 31% | 100% |
A0A1X0P926 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJ48 | Leishmania donovani | 70% | 99% |
A0A422NTW3 | Trypanosoma rangeli | 33% | 100% |
A4ICL4 | Leishmania infantum | 70% | 99% |
D0A2U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ASP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 99% |
P30777 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
P86935 | Trypanosoma brucei brucei | 34% | 100% |
P86936 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 35% | 100% |
Q1LZA0 | Bos taurus | 23% | 100% |
Q4Q1V6 | Leishmania major | 67% | 100% |
Q4V7R2 | Xenopus laevis | 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) | 24% | 100% |
Q94A15 | Arabidopsis thaliana | 25% | 100% |
Q9JJQ0 | Mus musculus | 23% | 100% |
Q9VZM5 | Drosophila melanogaster | 25% | 100% |
V5DRF7 | Trypanosoma cruzi | 34% | 100% |