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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
Related structures:
AlphaFold database: A4H9L4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 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:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 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:0046337 | phosphatidylethanolamine metabolic process | 6 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004306 | ethanolamine-phosphate cytidylyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0070567 | cytidylyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 46 | 54 | PF00400 | 0.263 |
DEG_SCF_FBW7_1 | 547 | 554 | PF00400 | 0.639 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.629 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.640 |
DOC_CKS1_1 | 548 | 553 | PF01111 | 0.648 |
DOC_CYCLIN_RxL_1 | 44 | 52 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 329 | 339 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 385 | 393 | PF00069 | 0.560 |
DOC_MAPK_HePTP_8 | 233 | 245 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 217 | 224 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 300 | 307 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 333 | 342 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.537 |
DOC_MAPK_NFAT4_5 | 217 | 225 | PF00069 | 0.449 |
DOC_MAPK_RevD_3 | 370 | 386 | PF00069 | 0.379 |
DOC_PP1_SILK_1 | 541 | 546 | PF00149 | 0.522 |
DOC_PP2B_LxvP_1 | 153 | 156 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.429 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.525 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.670 |
DOC_USP7_UBL2_3 | 331 | 335 | PF12436 | 0.577 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 154 | 164 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 47 | 56 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 494 | 501 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 563 | 570 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 575 | 582 | PF00244 | 0.664 |
LIG_Actin_WH2_2 | 91 | 106 | PF00022 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.449 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.359 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.344 |
LIG_EH1_1 | 282 | 290 | PF00400 | 0.449 |
LIG_EH1_1 | 411 | 419 | PF00400 | 0.522 |
LIG_eIF4E_1 | 334 | 340 | PF01652 | 0.581 |
LIG_eIF4E_1 | 412 | 418 | PF01652 | 0.549 |
LIG_eIF4E_1 | 515 | 521 | PF01652 | 0.400 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.499 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.242 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.358 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.395 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.560 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.595 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.341 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.363 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.476 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.623 |
LIG_IRF3_LxIS_1 | 178 | 184 | PF10401 | 0.451 |
LIG_LIR_Apic_2 | 474 | 478 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 525 | 530 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 532 | 538 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 158 | 164 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 280 | 291 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.365 |
LIG_LIR_LC3C_4 | 316 | 319 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.398 |
LIG_NRBOX | 175 | 181 | PF00104 | 0.363 |
LIG_NRBOX | 283 | 289 | PF00104 | 0.475 |
LIG_NRBOX | 395 | 401 | PF00104 | 0.635 |
LIG_NRBOX | 60 | 66 | PF00104 | 0.396 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.369 |
LIG_PTB_Apo_2 | 264 | 271 | PF02174 | 0.664 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.443 |
LIG_PTB_Phospho_1 | 264 | 270 | PF10480 | 0.663 |
LIG_PTB_Phospho_1 | 72 | 78 | PF10480 | 0.435 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.343 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.587 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.324 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.562 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.501 |
LIG_SH2_CRK | 535 | 539 | PF00017 | 0.504 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.322 |
LIG_SH2_GRB2like | 515 | 518 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.476 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.562 |
LIG_SH3_1 | 545 | 551 | PF00018 | 0.629 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.363 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.359 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.501 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.640 |
LIG_SH3_5 | 156 | 160 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 174 | 180 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 371 | 376 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 416 | 421 | PF11976 | 0.514 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.449 |
LIG_TRAF2_1 | 482 | 485 | PF00917 | 0.473 |
LIG_TRFH_1 | 350 | 354 | PF08558 | 0.413 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.475 |
LIG_TYR_ITIM | 513 | 518 | PF00017 | 0.562 |
LIG_UBA3_1 | 302 | 309 | PF00899 | 0.435 |
LIG_UBA3_1 | 327 | 335 | PF00899 | 0.569 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.344 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.629 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.556 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.328 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.357 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.487 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.667 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.655 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.363 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.461 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.350 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.755 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.718 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.707 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.333 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.514 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.537 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.410 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.531 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.373 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.623 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.453 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.545 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.419 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.393 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.336 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.342 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.525 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.455 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.312 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.326 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.475 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.476 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.397 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.720 |
MOD_PKB_1 | 197 | 205 | PF00069 | 0.604 |
MOD_PKB_1 | 561 | 569 | PF00069 | 0.597 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.567 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.447 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.343 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.518 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.375 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.700 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.567 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.320 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.335 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.342 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.362 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.376 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.351 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.339 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.530 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.512 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.375 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.566 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.541 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.427 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.629 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.476 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.562 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.642 |
MOD_SUMO_rev_2 | 568 | 577 | PF00179 | 0.721 |
MOD_SUMO_rev_2 | 87 | 97 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 458 | 463 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.518 |
TRG_ER_diLys_1 | 581 | 586 | PF00400 | 0.615 |
TRG_NLS_MonoExtC_3 | 330 | 335 | PF00514 | 0.512 |
TRG_NLS_MonoExtN_4 | 329 | 336 | PF00514 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 47 | 52 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I259 | Leptomonas seymouri | 79% | 100% |
A0A0S4JNN5 | Bodo saltans | 45% | 100% |
A0A1X0P717 | Trypanosomatidae | 61% | 100% |
A0A3Q8IA23 | Leishmania donovani | 92% | 99% |
A0A422P0J5 | Trypanosoma rangeli | 60% | 100% |
A4HY04 | Leishmania infantum | 92% | 99% |
D0A5A2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ARR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4QDQ6 | Leishmania major | 89% | 100% |
V5BEI8 | Trypanosoma cruzi | 59% | 100% |