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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HPT7
Term | Name | Level | Count |
---|---|---|---|
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 11 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 11 |
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 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:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003975 | UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016757 | glycosyltransferase activity | 3 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.176 |
CLV_MEL_PAP_1 | 181 | 187 | PF00089 | 0.529 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.383 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.351 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.356 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.368 |
DEG_SCF_FBW7_1 | 296 | 301 | PF00400 | 0.204 |
DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.363 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.273 |
DOC_CYCLIN_RxL_1 | 43 | 52 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 151 | 158 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 432 | 438 | PF00149 | 0.533 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.326 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.533 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.429 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.624 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 74 | 83 | PF00244 | 0.656 |
LIG_APCC_ABBA_1 | 424 | 429 | PF00400 | 0.581 |
LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.284 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.350 |
LIG_CaM_NSCaTE_8 | 196 | 203 | PF13499 | 0.245 |
LIG_CtBP_PxDLS_1 | 89 | 93 | PF00389 | 0.486 |
LIG_eIF4E_1 | 368 | 374 | PF01652 | 0.334 |
LIG_eIF4E_1 | 455 | 461 | PF01652 | 0.384 |
LIG_EVH1_2 | 207 | 211 | PF00568 | 0.176 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.396 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.313 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.324 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.253 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.422 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.591 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.467 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.468 |
LIG_GBD_Chelix_1 | 103 | 111 | PF00786 | 0.451 |
LIG_LIR_Gen_1 | 122 | 133 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 414 | 425 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 436 | 445 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 436 | 440 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.356 |
LIG_NRBOX | 318 | 324 | PF00104 | 0.451 |
LIG_NRBOX | 456 | 462 | PF00104 | 0.450 |
LIG_Pex14_2 | 109 | 113 | PF04695 | 0.198 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.329 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 229 | 232 | PF00017 | 0.339 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.176 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.190 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.411 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.310 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.329 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.417 |
LIG_SUMO_SIM_anti_2 | 134 | 139 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 173 | 178 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 24 | 30 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 275 | 282 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.379 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.374 |
LIG_UBA3_1 | 53 | 60 | PF00899 | 0.593 |
LIG_WRC_WIRS_1 | 456 | 461 | PF05994 | 0.516 |
MOD_CDK_SPK_2 | 38 | 43 | PF00069 | 0.427 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.379 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.474 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.536 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.474 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.309 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.315 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.120 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.367 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.319 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.459 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.349 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.528 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.511 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.529 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.281 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.256 |
MOD_N-GLC_2 | 11 | 13 | PF02516 | 0.438 |
MOD_N-GLC_2 | 225 | 227 | PF02516 | 0.376 |
MOD_N-GLC_2 | 286 | 288 | PF02516 | 0.198 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.384 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.356 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.401 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.306 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.306 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.490 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.380 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.348 |
MOD_PKB_1 | 398 | 406 | PF00069 | 0.590 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.492 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.418 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.368 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.370 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.339 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.318 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.326 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.313 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.282 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.478 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.430 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.418 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.273 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 429 | 436 | PF00179 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.120 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUV1 | Leptomonas seymouri | 70% | 100% |
A0A0S4IKK6 | Bodo saltans | 49% | 100% |
A0A3Q8IJH0 | Leishmania donovani | 85% | 100% |
A0A3R7MVB5 | Trypanosoma rangeli | 47% | 100% |
A4IE55 | Leishmania infantum | 86% | 100% |
D0A8Q1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ATK2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
P07286 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P0CD61 | Dictyostelium discoideum | 36% | 100% |
P23338 | Cricetulus longicaudatus | 35% | 100% |
P24140 | Cricetulus griseus | 35% | 100% |
P42864 | Leishmania amazonensis | 84% | 100% |
P42867 | Mus musculus | 36% | 100% |
P42881 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q4Q0Z6 | Leishmania major | 84% | 100% |
Q5EA65 | Bos taurus | 35% | 100% |
Q9H3H5 | Homo sapiens | 35% | 100% |
V5B6U2 | Trypanosoma cruzi | 48% | 100% |