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:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0012505 | endomembrane system | 2 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4QE99
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0036149 | phosphatidylinositol acyl-chain remodeling | 7 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.532 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.431 |
CLV_PCSK_FUR_1 | 460 | 464 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.372 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.185 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.308 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.271 |
DEG_MDM2_SWIB_1 | 415 | 423 | PF02201 | 0.311 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.632 |
DEG_SCF_FBW7_1 | 450 | 456 | PF00400 | 0.488 |
DOC_CDC14_PxL_1 | 164 | 172 | PF14671 | 0.451 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.496 |
DOC_CYCLIN_RxL_1 | 106 | 114 | PF00134 | 0.531 |
DOC_CYCLIN_RxL_1 | 175 | 183 | PF00134 | 0.455 |
DOC_CYCLIN_RxL_1 | 332 | 343 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 293 | 299 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 387 | 395 | PF00069 | 0.518 |
DOC_MAPK_JIP1_4 | 280 | 286 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.449 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.576 |
DOC_PP2B_PxIxI_1 | 206 | 212 | PF00149 | 0.435 |
DOC_SPAK_OSR1_1 | 344 | 348 | PF12202 | 0.417 |
DOC_USP7_UBL2_3 | 161 | 165 | PF12436 | 0.470 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 150 | 160 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 417 | 427 | PF00244 | 0.302 |
LIG_APCC_ABBA_1 | 209 | 214 | PF00400 | 0.429 |
LIG_CaM_IQ_9 | 455 | 471 | PF13499 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 138 | 146 | PF00928 | 0.432 |
LIG_EH1_1 | 403 | 411 | PF00400 | 0.173 |
LIG_eIF4E_1 | 404 | 410 | PF01652 | 0.173 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.430 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.460 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.447 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.489 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.536 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.366 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.531 |
LIG_LIR_Apic_2 | 273 | 277 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 421 | 432 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.182 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.424 |
LIG_MAD2 | 115 | 123 | PF02301 | 0.510 |
LIG_PCNA_PIPBox_1 | 193 | 202 | PF02747 | 0.455 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.464 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.527 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.398 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.379 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.304 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.627 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.514 |
LIG_SH2_GRB2like | 447 | 450 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.469 |
LIG_SH2_SRC | 447 | 450 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.467 |
LIG_SH3_2 | 120 | 125 | PF14604 | 0.512 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.473 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.429 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.385 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.580 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.390 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.596 |
LIG_SUMO_SIM_anti_2 | 205 | 212 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 246 | 254 | PF11976 | 0.515 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.522 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.449 |
LIG_UBA3_1 | 152 | 161 | PF00899 | 0.540 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.451 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.304 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.432 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.623 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.346 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.563 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.520 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.467 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.549 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.455 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.356 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.330 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.238 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.538 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.577 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.483 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.415 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.532 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.582 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.451 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.288 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.205 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.559 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.542 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.457 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.508 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.508 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.495 |
MOD_SUMO_rev_2 | 162 | 167 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 467 | 476 | PF00179 | 0.618 |
TRG_AP2beta_CARGO_1 | 175 | 184 | PF09066 | 0.435 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.609 |
TRG_ER_diLys_1 | 472 | 477 | PF00400 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 463 | 467 | PF00026 | 0.252 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC7 | Leptomonas seymouri | 58% | 100% |
A0A0S4J7G6 | Bodo saltans | 31% | 100% |
A0A1X0NU94 | Trypanosomatidae | 38% | 100% |
A0A3Q8IE09 | Leishmania donovani | 96% | 100% |
A0A422NH08 | Trypanosoma rangeli | 42% | 100% |
A4H937 | Leishmania braziliensis | 75% | 100% |
A4HXG9 | Leishmania infantum | 96% | 100% |
C9ZP55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AR64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q20800 | Caenorhabditis elegans | 27% | 100% |
Q5F3X0 | Gallus gallus | 28% | 100% |
V5BF39 | Trypanosoma cruzi | 40% | 100% |