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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HJG0
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 13 |
GO:0006643 | membrane lipid metabolic process | 4 | 13 |
GO:0006665 | sphingolipid metabolic process | 4 | 13 |
GO:0006672 | ceramide metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0008610 | lipid biosynthetic process | 4 | 13 |
GO:0009058 | biosynthetic process | 2 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043603 | amide metabolic process | 3 | 13 |
GO:0043604 | amide biosynthetic process | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044249 | cellular biosynthetic process | 3 | 13 |
GO:0044255 | cellular lipid metabolic process | 3 | 13 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 13 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 13 |
GO:0046513 | ceramide biosynthetic process | 5 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 13 |
GO:1901576 | organic substance biosynthetic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0016410 | N-acyltransferase activity | 5 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016746 | acyltransferase activity | 3 | 13 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 13 |
GO:0050291 | sphingosine N-acyltransferase activity | 6 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 246 | 252 | PF00089 | 0.513 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.537 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.222 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.166 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.561 |
DEG_SPOP_SBC_1 | 436 | 440 | PF00917 | 0.557 |
DOC_CKS1_1 | 442 | 447 | PF01111 | 0.551 |
DOC_CYCLIN_RxL_1 | 92 | 103 | PF00134 | 0.208 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 191 | PF00134 | 0.313 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.250 |
DOC_MAPK_gen_1 | 136 | 144 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 138 | 145 | PF00149 | 0.471 |
DOC_PP1_RVXF_1 | 93 | 100 | PF00149 | 0.218 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.400 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.211 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.548 |
DOC_SPAK_OSR1_1 | 104 | 108 | PF12202 | 0.503 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.495 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.320 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.753 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 305 | 315 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 46 | 54 | PF00244 | 0.359 |
LIG_Actin_WH2_2 | 33 | 48 | PF00022 | 0.296 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.426 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.237 |
LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.159 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.283 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.678 |
LIG_Clathr_ClatBox_1 | 213 | 217 | PF01394 | 0.399 |
LIG_EH1_1 | 231 | 239 | PF00400 | 0.309 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.247 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.261 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.626 |
LIG_GBD_Chelix_1 | 355 | 363 | PF00786 | 0.284 |
LIG_GBD_Chelix_1 | 89 | 97 | PF00786 | 0.159 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 439 | 445 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 312 | 323 | PF02991 | 0.192 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.160 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.308 |
LIG_MLH1_MIPbox_1 | 321 | 325 | PF16413 | 0.283 |
LIG_MYND_1 | 79 | 83 | PF01753 | 0.178 |
LIG_NRBOX | 354 | 360 | PF00104 | 0.237 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.302 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.343 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.237 |
LIG_REV1ctd_RIR_1 | 322 | 332 | PF16727 | 0.253 |
LIG_RPA_C_Fungi | 116 | 128 | PF08784 | 0.399 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.399 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.348 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.500 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.167 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 189 | 193 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 19 | 23 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.159 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.249 |
LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.180 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.398 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.277 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 235 | 240 | PF11976 | 0.246 |
LIG_SUMO_SIM_anti_2 | 371 | 376 | PF11976 | 0.159 |
LIG_SUMO_SIM_anti_2 | 74 | 79 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 259 | 268 | PF11976 | 0.259 |
LIG_TRAF2_1 | 191 | 194 | PF00917 | 0.369 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.273 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.279 |
LIG_UBA3_1 | 213 | 221 | PF00899 | 0.302 |
LIG_UBA3_1 | 374 | 383 | PF00899 | 0.159 |
MOD_CDK_SPK_2 | 131 | 136 | PF00069 | 0.386 |
MOD_CDK_SPxK_1 | 441 | 447 | PF00069 | 0.445 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.592 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.546 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.509 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.540 |
MOD_Cter_Amidation | 125 | 128 | PF01082 | 0.491 |
MOD_Cter_Amidation | 384 | 387 | PF01082 | 0.382 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.381 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.416 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.446 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.424 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.551 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.347 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.341 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.309 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.576 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.501 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.709 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.533 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.586 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.548 |
MOD_N-GLC_2 | 314 | 316 | PF02516 | 0.343 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.362 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.350 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.249 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.398 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.351 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.693 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.159 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.279 |
MOD_PKA_1 | 452 | 458 | PF00069 | 0.607 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.510 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.510 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.607 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.379 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.411 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.235 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.341 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.287 |
MOD_Plk_2-3 | 389 | 395 | PF00069 | 0.471 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.282 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.429 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.328 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.346 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.283 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.337 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.272 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.382 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.561 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.456 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.414 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.167 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 95 | 100 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2N8 | Leptomonas seymouri | 64% | 100% |
A0A0S4JIF9 | Bodo saltans | 35% | 100% |
A0A1X0NPU5 | Trypanosomatidae | 44% | 100% |
A0A1X0NPY1 | Trypanosomatidae | 46% | 100% |
A0A3S7X4J5 | Leishmania donovani | 70% | 100% |
A0A422MNN3 | Trypanosoma rangeli | 46% | 100% |
A4I6V5 | Leishmania infantum | 70% | 100% |
C9ZMC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZWR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B1X8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
G5ED45 | Caenorhabditis elegans | 26% | 100% |
Q4Q684 | Leishmania major | 69% | 100% |
Q9D6J1 | Mus musculus | 31% | 100% |
Q9LDF2 | Arabidopsis thaliana | 26% | 100% |