| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005886 | plasma membrane | 3 | 1 |
| GO:0016020 | membrane | 2 | 1 |
| GO:0020016 | ciliary pocket | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB28
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006793 | phosphorus metabolic process | 3 | 10 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
| GO:0008152 | metabolic process | 1 | 10 |
| GO:0009987 | cellular process | 1 | 10 |
| GO:0016310 | phosphorylation | 5 | 10 |
| GO:0044237 | cellular metabolic process | 2 | 10 |
| GO:0006629 | lipid metabolic process | 3 | 1 |
| GO:0006644 | phospholipid metabolic process | 4 | 1 |
| GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
| GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 1 |
| GO:0008610 | lipid biosynthetic process | 4 | 1 |
| GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
| GO:0009058 | biosynthetic process | 2 | 1 |
| GO:0019637 | organophosphate metabolic process | 3 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044249 | cellular biosynthetic process | 3 | 1 |
| GO:0044255 | cellular lipid metabolic process | 3 | 1 |
| GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
| GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
| GO:0046486 | glycerolipid metabolic process | 4 | 1 |
| GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
| GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
| GO:1901576 | organic substance biosynthetic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 10 |
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0005488 | binding | 1 | 10 |
| GO:0005524 | ATP binding | 5 | 10 |
| GO:0016301 | kinase activity | 4 | 10 |
| GO:0016307 | phosphatidylinositol phosphate kinase activity | 5 | 10 |
| GO:0016740 | transferase activity | 2 | 10 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
| GO:0017076 | purine nucleotide binding | 4 | 10 |
| GO:0030554 | adenyl nucleotide binding | 5 | 10 |
| GO:0032553 | ribonucleotide binding | 3 | 10 |
| GO:0032555 | purine ribonucleotide binding | 4 | 10 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
| GO:0036094 | small molecule binding | 2 | 10 |
| GO:0043167 | ion binding | 2 | 10 |
| GO:0043168 | anion binding | 3 | 10 |
| GO:0097159 | organic cyclic compound binding | 2 | 10 |
| GO:0097367 | carbohydrate derivative binding | 2 | 10 |
| GO:1901265 | nucleoside phosphate binding | 3 | 10 |
| GO:1901363 | heterocyclic compound binding | 2 | 10 |
| GO:0016308 | 1-phosphatidylinositol-4-phosphate 5-kinase activity | 6 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.623 |
| CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.377 |
| CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.319 |
| CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.319 |
| CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.319 |
| CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.368 |
| CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.527 |
| CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.375 |
| CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.319 |
| CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.319 |
| CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.423 |
| CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.426 |
| CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.375 |
| CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.375 |
| CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.423 |
| CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.426 |
| CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.751 |
| CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.370 |
| CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.341 |
| CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.461 |
| CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.295 |
| CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.613 |
| CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.461 |
| CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.394 |
| CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.422 |
| DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.630 |
| DEG_SCF_FBW7_1 | 256 | 262 | PF00400 | 0.322 |
| DOC_CKS1_1 | 256 | 261 | PF01111 | 0.418 |
| DOC_CYCLIN_RxL_1 | 2 | 10 | PF00134 | 0.682 |
| DOC_CYCLIN_RxL_1 | 373 | 384 | PF00134 | 0.250 |
| DOC_MAPK_gen_1 | 315 | 324 | PF00069 | 0.412 |
| DOC_MAPK_gen_1 | 59 | 67 | PF00069 | 0.289 |
| DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.203 |
| DOC_MAPK_MEF2A_6 | 60 | 69 | PF00069 | 0.273 |
| DOC_MAPK_RevD_3 | 67 | 82 | PF00069 | 0.418 |
| DOC_PP1_RVXF_1 | 535 | 542 | PF00149 | 0.319 |
| DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.319 |
| DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.677 |
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.749 |
| DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.319 |
| DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.536 |
| DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.351 |
| DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.325 |
| DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.377 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.762 |
| DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.359 |
| LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.689 |
| LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.649 |
| LIG_14-3-3_CanoR_1 | 318 | 326 | PF00244 | 0.345 |
| LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.357 |
| LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.428 |
| LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.375 |
| LIG_14-3-3_CanoR_1 | 473 | 482 | PF00244 | 0.343 |
| LIG_14-3-3_CanoR_1 | 523 | 531 | PF00244 | 0.415 |
| LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.507 |
| LIG_Actin_WH2_2 | 302 | 317 | PF00022 | 0.461 |
| LIG_Actin_WH2_2 | 426 | 441 | PF00022 | 0.308 |
| LIG_APCC_ABBAyCdc20_2 | 465 | 471 | PF00400 | 0.203 |
| LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.450 |
| LIG_BRCT_BRCA1_1 | 465 | 469 | PF00533 | 0.203 |
| LIG_Clathr_ClatBox_1 | 380 | 384 | PF01394 | 0.203 |
| LIG_EH_1 | 299 | 303 | PF12763 | 0.461 |
| LIG_EVH1_2 | 216 | 220 | PF00568 | 0.551 |
| LIG_FHA_1 | 129 | 135 | PF00498 | 0.666 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.749 |
| LIG_FHA_1 | 331 | 337 | PF00498 | 0.404 |
| LIG_FHA_1 | 428 | 434 | PF00498 | 0.437 |
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.443 |
| LIG_FHA_2 | 196 | 202 | PF00498 | 0.723 |
| LIG_FHA_2 | 219 | 225 | PF00498 | 0.425 |
| LIG_FHA_2 | 275 | 281 | PF00498 | 0.325 |
| LIG_FHA_2 | 333 | 339 | PF00498 | 0.343 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.363 |
| LIG_FHA_2 | 446 | 452 | PF00498 | 0.304 |
| LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.459 |
| LIG_LIR_Gen_1 | 241 | 248 | PF02991 | 0.398 |
| LIG_LIR_Gen_1 | 251 | 259 | PF02991 | 0.404 |
| LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.343 |
| LIG_LIR_Gen_1 | 320 | 331 | PF02991 | 0.420 |
| LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.319 |
| LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.622 |
| LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.397 |
| LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.381 |
| LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.403 |
| LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.404 |
| LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.330 |
| LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.319 |
| LIG_LIR_Nem_3 | 493 | 499 | PF02991 | 0.319 |
| LIG_PDZ_Class_2 | 542 | 547 | PF00595 | 0.319 |
| LIG_REV1ctd_RIR_1 | 265 | 275 | PF16727 | 0.319 |
| LIG_SH2_CRK | 169 | 173 | PF00017 | 0.619 |
| LIG_SH2_CRK | 401 | 405 | PF00017 | 0.319 |
| LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.503 |
| LIG_SH2_NCK_1 | 446 | 450 | PF00017 | 0.203 |
| LIG_SH2_PTP2 | 496 | 499 | PF00017 | 0.319 |
| LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.319 |
| LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.202 |
| LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.391 |
| LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.420 |
| LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.333 |
| LIG_SH3_1 | 81 | 87 | PF00018 | 0.468 |
| LIG_SH3_2 | 84 | 89 | PF14604 | 0.472 |
| LIG_SH3_3 | 81 | 87 | PF00018 | 0.468 |
| LIG_SUMO_SIM_par_1 | 379 | 384 | PF11976 | 0.359 |
| LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.343 |
| LIG_TRFH_1 | 302 | 306 | PF08558 | 0.333 |
| LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.319 |
| LIG_TYR_ITSM | 240 | 247 | PF00017 | 0.266 |
| LIG_UBA3_1 | 380 | 388 | PF00899 | 0.321 |
| MOD_CDK_SPxK_1 | 255 | 261 | PF00069 | 0.319 |
| MOD_CK1_1 | 170 | 176 | PF00069 | 0.625 |
| MOD_CK1_1 | 181 | 187 | PF00069 | 0.505 |
| MOD_CK1_1 | 255 | 261 | PF00069 | 0.319 |
| MOD_CK1_1 | 45 | 51 | PF00069 | 0.669 |
| MOD_CK1_1 | 92 | 98 | PF00069 | 0.559 |
| MOD_CK2_1 | 201 | 207 | PF00069 | 0.670 |
| MOD_CK2_1 | 274 | 280 | PF00069 | 0.328 |
| MOD_CK2_1 | 332 | 338 | PF00069 | 0.343 |
| MOD_CK2_1 | 349 | 355 | PF00069 | 0.319 |
| MOD_CK2_1 | 74 | 80 | PF00069 | 0.543 |
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.729 |
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.747 |
| MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.319 |
| MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.736 |
| MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.385 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.555 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.618 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.691 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.523 |
| MOD_GSK3_1 | 248 | 255 | PF00069 | 0.319 |
| MOD_GSK3_1 | 276 | 283 | PF00069 | 0.319 |
| MOD_GSK3_1 | 427 | 434 | PF00069 | 0.272 |
| MOD_GSK3_1 | 440 | 447 | PF00069 | 0.273 |
| MOD_GSK3_1 | 89 | 96 | PF00069 | 0.477 |
| MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.494 |
| MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.579 |
| MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.450 |
| MOD_NEK2_1 | 126 | 131 | PF00069 | 0.533 |
| MOD_NEK2_1 | 172 | 177 | PF00069 | 0.724 |
| MOD_NEK2_1 | 179 | 184 | PF00069 | 0.754 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.610 |
| MOD_NEK2_1 | 248 | 253 | PF00069 | 0.319 |
| MOD_NEK2_1 | 330 | 335 | PF00069 | 0.368 |
| MOD_NEK2_1 | 342 | 347 | PF00069 | 0.243 |
| MOD_NEK2_1 | 393 | 398 | PF00069 | 0.325 |
| MOD_NEK2_1 | 399 | 404 | PF00069 | 0.310 |
| MOD_NEK2_1 | 429 | 434 | PF00069 | 0.363 |
| MOD_NEK2_1 | 444 | 449 | PF00069 | 0.189 |
| MOD_NEK2_1 | 463 | 468 | PF00069 | 0.286 |
| MOD_NEK2_1 | 541 | 546 | PF00069 | 0.319 |
| MOD_NEK2_1 | 7 | 12 | PF00069 | 0.666 |
| MOD_NEK2_1 | 99 | 104 | PF00069 | 0.549 |
| MOD_PIKK_1 | 193 | 199 | PF00454 | 0.747 |
| MOD_PIKK_1 | 359 | 365 | PF00454 | 0.319 |
| MOD_PK_1 | 252 | 258 | PF00069 | 0.418 |
| MOD_PK_1 | 89 | 95 | PF00069 | 0.521 |
| MOD_PKA_1 | 356 | 362 | PF00069 | 0.348 |
| MOD_PKA_1 | 524 | 530 | PF00069 | 0.375 |
| MOD_PKA_2 | 126 | 132 | PF00069 | 0.669 |
| MOD_PKA_2 | 317 | 323 | PF00069 | 0.345 |
| MOD_PKA_2 | 356 | 362 | PF00069 | 0.391 |
| MOD_PKA_2 | 524 | 530 | PF00069 | 0.418 |
| MOD_Plk_1 | 146 | 152 | PF00069 | 0.722 |
| MOD_Plk_1 | 179 | 185 | PF00069 | 0.755 |
| MOD_Plk_1 | 239 | 245 | PF00069 | 0.260 |
| MOD_Plk_1 | 399 | 405 | PF00069 | 0.319 |
| MOD_Plk_1 | 434 | 440 | PF00069 | 0.308 |
| MOD_Plk_1 | 89 | 95 | PF00069 | 0.422 |
| MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.672 |
| MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.719 |
| MOD_Plk_4 | 195 | 201 | PF00069 | 0.633 |
| MOD_Plk_4 | 399 | 405 | PF00069 | 0.324 |
| MOD_Plk_4 | 516 | 522 | PF00069 | 0.393 |
| MOD_Plk_4 | 541 | 547 | PF00069 | 0.328 |
| MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.536 |
| MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.349 |
| MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.325 |
| MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.377 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.755 |
| MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.359 |
| MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.645 |
| MOD_SUMO_rev_2 | 338 | 345 | PF00179 | 0.319 |
| MOD_SUMO_rev_2 | 519 | 526 | PF00179 | 0.461 |
| TRG_DiLeu_BaEn_1 | 377 | 382 | PF01217 | 0.418 |
| TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.203 |
| TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.678 |
| TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.363 |
| TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.366 |
| TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.306 |
| TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.319 |
| TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.319 |
| TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.407 |
| TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.449 |
| TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.475 |
| TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.368 |
| TRG_NLS_Bipartite_1 | 103 | 123 | PF00514 | 0.439 |
| TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.375 |
| TRG_Pf-PMV_PEXEL_1 | 379 | 384 | PF00026 | 0.343 |
| TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.569 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PCT9 | Leptomonas seymouri | 62% | 100% |
| A0A1X0P9B0 | Trypanosomatidae | 24% | 100% |
| A0A1X0PB79 | Trypanosomatidae | 46% | 100% |
| A0A381MTN1 | Leishmania infantum | 79% | 100% |
| A0A3Q8ILB5 | Leishmania donovani | 79% | 100% |
| A4HNP5 | Leishmania braziliensis | 22% | 100% |
| C9ZM20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| E9B598 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
| O13853 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 74% |
| O48709 | Arabidopsis thaliana | 32% | 78% |
| Q4Q2N5 | Leishmania major | 77% | 100% |
| Q56YP2 | Arabidopsis thaliana | 30% | 73% |
| Q6EX42 | Oryza sativa subsp. japonica | 31% | 68% |
| Q8L796 | Arabidopsis thaliana | 31% | 73% |
| Q8L850 | Arabidopsis thaliana | 30% | 67% |
| Q8RY89 | Arabidopsis thaliana | 28% | 71% |
| Q9M149 | Arabidopsis thaliana | 26% | 100% |
| Q9SUI2 | Arabidopsis thaliana | 30% | 73% |
| V5BA13 | Trypanosoma cruzi | 27% | 100% |
| V5BV28 | Trypanosoma cruzi | 47% | 100% |