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:0005635 | nuclear envelope | 4 | 2 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0031967 | organelle envelope | 3 | 2 |
GO:0031975 | envelope | 2 | 2 |
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 | 12 |
Related structures:
AlphaFold database: Q4Q0H0
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 10 |
GO:0006644 | phospholipid metabolic process | 4 | 10 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008610 | lipid biosynthetic process | 4 | 10 |
GO:0008654 | phospholipid biosynthetic process | 5 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019637 | organophosphate metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 10 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 2 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 2 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090407 | organophosphate biosynthetic process | 4 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004142 | diacylglycerol cholinephosphotransferase activity | 6 | 4 |
GO:0004307 | ethanolaminephosphotransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0017169 | CDP-alcohol phosphatidyltransferase activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.368 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.407 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.469 |
DEG_ODPH_VHL_1 | 284 | 297 | PF01847 | 0.329 |
DEG_ODPH_VHL_1 | 61 | 73 | PF01847 | 0.498 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.299 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 277 | 284 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.299 |
DOC_PP1_RVXF_1 | 336 | 343 | PF00149 | 0.522 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.315 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.695 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 158 | 167 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 254 | 272 | PF00022 | 0.430 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.373 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.235 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.334 |
LIG_eIF4E_1 | 99 | 105 | PF01652 | 0.299 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.290 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.485 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.361 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.328 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.441 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.288 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.331 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.300 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.407 |
LIG_HP1_1 | 141 | 145 | PF01393 | 0.212 |
LIG_IRF3_LxIS_1 | 400 | 407 | PF10401 | 0.558 |
LIG_LIR_Apic_2 | 136 | 141 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 339 | 350 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.473 |
LIG_LIR_LC3C_4 | 291 | 295 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.387 |
LIG_LYPXL_yS_3 | 224 | 227 | PF13949 | 0.335 |
LIG_MLH1_MIPbox_1 | 228 | 232 | PF16413 | 0.418 |
LIG_MYND_1 | 226 | 230 | PF01753 | 0.255 |
LIG_PCNA_PIPBox_1 | 153 | 162 | PF02747 | 0.352 |
LIG_PCNA_yPIPBox_3 | 146 | 158 | PF02747 | 0.446 |
LIG_Pex14_1 | 95 | 99 | PF04695 | 0.299 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.315 |
LIG_Rb_pABgroove_1 | 125 | 133 | PF01858 | 0.447 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.384 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.570 |
LIG_SH2_GRB2like | 186 | 189 | PF00017 | 0.539 |
LIG_SH2_GRB2like | 49 | 52 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.576 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.539 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.315 |
LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.271 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.588 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.345 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.405 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.521 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.362 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.347 |
LIG_SUMO_SIM_anti_2 | 140 | 146 | PF11976 | 0.212 |
LIG_SUMO_SIM_anti_2 | 34 | 42 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 405 | 410 | PF11976 | 0.548 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.550 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.337 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.407 |
LIG_UBA3_1 | 408 | 415 | PF00899 | 0.573 |
LIG_WW_1 | 21 | 24 | PF00397 | 0.547 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.408 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.253 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.403 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.288 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.501 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.417 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.508 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.476 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.530 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.407 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.418 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.579 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.628 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.363 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.396 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.368 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.474 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.323 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.375 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.371 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.583 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.299 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.532 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.384 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.517 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.448 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.229 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.297 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.313 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.340 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.300 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.464 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.394 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.279 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.493 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.297 |
MOD_NEK2_2 | 235 | 240 | PF00069 | 0.361 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.339 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.472 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.542 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.614 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.447 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.567 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.323 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.419 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.351 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.324 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.273 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.497 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.382 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.395 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.165 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.336 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.520 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.488 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.323 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.348 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.487 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.209 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.250 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.478 |
MOD_SUMO_rev_2 | 111 | 118 | PF00179 | 0.447 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.334 |
TRG_NLS_MonoExtN_4 | 26 | 33 | PF00514 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I260 | Leptomonas seymouri | 63% | 100% |
A0A0S4JA45 | Bodo saltans | 38% | 95% |
A0A1X0NLI0 | Trypanosomatidae | 49% | 92% |
A0A3Q8IRT0 | Leishmania donovani | 94% | 100% |
A0A3R7NAX1 | Trypanosoma rangeli | 48% | 97% |
A4HQA8 | Leishmania braziliensis | 81% | 100% |
A4IE03 | Leishmania infantum | 94% | 100% |
D0A400 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
E9AU25 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O82567 | Arabidopsis thaliana | 31% | 100% |
O82568 | Arabidopsis thaliana | 32% | 100% |
P17898 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q54XM0 | Dictyostelium discoideum | 30% | 100% |
Q550W1 | Dictyostelium discoideum | 29% | 100% |
Q55AQ3 | Dictyostelium discoideum | 31% | 100% |
V5B3K4 | Trypanosoma cruzi | 48% | 96% |