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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9B6H2
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0008654 | phospholipid biosynthetic process | 5 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0043048 | dolichyl monophosphate biosynthetic process | 6 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0016310 | phosphorylation | 5 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004168 | dolichol kinase activity | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.299 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.377 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.305 |
CLV_PCSK_PC7_1 | 281 | 287 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.370 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.320 |
DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.236 |
DOC_MAPK_gen_1 | 206 | 218 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 285 | 294 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 22 | 30 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.404 |
DOC_MAPK_NFAT4_5 | 22 | 30 | PF00069 | 0.321 |
DOC_MAPK_NFAT4_5 | 355 | 363 | PF00069 | 0.384 |
DOC_PP1_RVXF_1 | 520 | 527 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.302 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.258 |
DOC_PP2B_LxvP_1 | 511 | 514 | PF13499 | 0.271 |
DOC_PP2B_LxvP_1 | 539 | 542 | PF13499 | 0.548 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.673 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 255 | 260 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.251 |
LIG_APCC_ABBAyCdc20_2 | 426 | 432 | PF00400 | 0.683 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.388 |
LIG_Clathr_ClatBox_1 | 512 | 516 | PF01394 | 0.292 |
LIG_deltaCOP1_diTrp_1 | 516 | 526 | PF00928 | 0.478 |
LIG_EH1_1 | 363 | 371 | PF00400 | 0.281 |
LIG_eIF4E_1 | 424 | 430 | PF01652 | 0.587 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.453 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.339 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.335 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.358 |
LIG_GBD_Chelix_1 | 224 | 232 | PF00786 | 0.337 |
LIG_HP1_1 | 498 | 502 | PF01393 | 0.404 |
LIG_IRF3_LxIS_1 | 227 | 234 | PF10401 | 0.393 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 191 | 197 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 475 | 484 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 507 | 515 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.171 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 475 | 479 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 507 | 512 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.335 |
LIG_NRBOX | 507 | 513 | PF00104 | 0.404 |
LIG_PALB2_WD40_1 | 258 | 266 | PF16756 | 0.292 |
LIG_PCNA_TLS_4 | 418 | 426 | PF02747 | 0.639 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.286 |
LIG_PTB_Apo_2 | 424 | 431 | PF02174 | 0.541 |
LIG_REV1ctd_RIR_1 | 112 | 119 | PF16727 | 0.404 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.289 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 55 | 61 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 384 | 389 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 459 | 465 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.206 |
LIG_SUMO_SIM_par_1 | 498 | 504 | PF11976 | 0.184 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.335 |
LIG_TRFH_1 | 263 | 267 | PF08558 | 0.292 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.289 |
LIG_TYR_ITSM | 164 | 171 | PF00017 | 0.368 |
LIG_UBA3_1 | 113 | 117 | PF00899 | 0.292 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.171 |
LIG_WRC_WIRS_1 | 473 | 478 | PF05994 | 0.301 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.597 |
MOD_CDK_SPxxK_3 | 67 | 74 | PF00069 | 0.597 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.472 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.393 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.500 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.603 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.697 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.283 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.305 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.404 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.386 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.337 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.580 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.285 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.405 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.294 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.529 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.280 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.663 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.367 |
MOD_LATS_1 | 253 | 259 | PF00433 | 0.165 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.324 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.293 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.286 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.490 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.284 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.188 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.291 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.342 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.387 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.276 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.304 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.439 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.298 |
MOD_PK_1 | 373 | 379 | PF00069 | 0.363 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.610 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.451 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.215 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.522 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.519 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.638 |
MOD_PKB_1 | 371 | 379 | PF00069 | 0.354 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.298 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.542 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.493 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.314 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.416 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.339 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.332 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.341 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.200 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.271 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.288 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.175 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.341 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.271 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.297 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.672 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.595 |
MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.289 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.355 |
TRG_NLS_MonoExtN_4 | 208 | 215 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ90 | Leptomonas seymouri | 75% | 91% |
A0A1X0P5F5 | Trypanosomatidae | 49% | 100% |
A0A3Q8IJJ2 | Leishmania donovani | 92% | 100% |
A0A3R7KY54 | Trypanosoma rangeli | 49% | 100% |
A4HMW0 | Leishmania braziliensis | 85% | 100% |
A4IBI1 | Leishmania infantum | 93% | 100% |
C9ZZ59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9AFB7 | Leishmania major | 92% | 100% |
V5BTH9 | Trypanosoma cruzi | 50% | 100% |