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:0005789 | endoplasmic reticulum membrane | 4 | 9 |
GO:0016020 | membrane | 2 | 11 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
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: A4HFS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006066 | alcohol metabolic process | 3 | 10 |
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 10 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 10 |
GO:0006629 | lipid metabolic process | 3 | 10 |
GO:0006720 | isoprenoid metabolic process | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008300 | isoprenoid catabolic process | 5 | 10 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016042 | lipid catabolic process | 4 | 10 |
GO:0016093 | polyprenol metabolic process | 4 | 10 |
GO:0016095 | polyprenol catabolic process | 5 | 10 |
GO:0019348 | dolichol metabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044242 | cellular lipid catabolic process | 4 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 10 |
GO:0044281 | small molecule metabolic process | 2 | 10 |
GO:0044282 | small molecule catabolic process | 3 | 10 |
GO:0046164 | alcohol catabolic process | 4 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 10 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 10 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 10 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0016094 | polyprenol biosynthetic process | 5 | 1 |
GO:0019408 | dolichol biosynthetic process | 6 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003865 | 3-oxo-5-alpha-steroid 4-dehydrogenase activity | 5 | 10 |
GO:0016229 | steroid dehydrogenase activity | 3 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 10 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 9 |
GO:0033765 | steroid dehydrogenase activity, acting on the CH-CH group of donors | 4 | 10 |
GO:0102389 | polyprenol reductase activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.274 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.526 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.276 |
DEG_SCF_TRCP1_1 | 123 | 128 | PF00400 | 0.321 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.451 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.307 |
DOC_CDC14_PxL_1 | 145 | 153 | PF14671 | 0.181 |
DOC_CYCLIN_yCln2_LP_2 | 136 | 142 | PF00134 | 0.366 |
DOC_CYCLIN_yCln2_LP_2 | 289 | 295 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 93 | 103 | PF00069 | 0.475 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.537 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.612 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 96 | 101 | PF00244 | 0.485 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.429 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 262 | 268 | PF00928 | 0.478 |
LIG_EH1_1 | 102 | 110 | PF00400 | 0.311 |
LIG_EH1_1 | 326 | 334 | PF00400 | 0.285 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.300 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.306 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.438 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.238 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.585 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.538 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.475 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.291 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.600 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.367 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.513 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.487 |
LIG_GBD_Chelix_1 | 415 | 423 | PF00786 | 0.294 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 19 | 30 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 199 | 204 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 99 | 108 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 199 | 203 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.288 |
LIG_Pex14_1 | 18 | 22 | PF04695 | 0.364 |
LIG_Pex14_1 | 209 | 213 | PF04695 | 0.249 |
LIG_Pex14_2 | 115 | 119 | PF04695 | 0.384 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.582 |
LIG_Pex14_2 | 466 | 470 | PF04695 | 0.580 |
LIG_Rb_LxCxE_1 | 1 | 20 | PF01857 | 0.229 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 200 | 204 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.455 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.387 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 19 | 27 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 331 | 338 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.192 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 331 | 338 | PF11976 | 0.414 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.658 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.572 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.407 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.411 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.369 |
MOD_CMANNOS | 89 | 92 | PF00535 | 0.281 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.598 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.655 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.541 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.356 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.645 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.614 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.413 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.414 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.558 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.662 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.622 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.242 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.372 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.181 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.403 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.581 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.526 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.619 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.385 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.447 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.448 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.476 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.336 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.412 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.249 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.325 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.259 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.286 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.389 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.702 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.617 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.190 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.400 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.363 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.263 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.446 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.396 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.267 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.331 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.412 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.453 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.348 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.231 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.254 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.343 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.438 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.392 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.414 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.401 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.274 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.364 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.243 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.577 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.701 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.545 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.480 |
MOD_SUMO_rev_2 | 55 | 65 | PF00179 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 146 | 151 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXY2 | Leptomonas seymouri | 42% | 100% |
A0A0S4JTN4 | Bodo saltans | 29% | 100% |
A0A1X0P483 | Trypanosomatidae | 30% | 100% |
A0A3Q8ICQ8 | Leishmania donovani | 72% | 100% |
A0A3R7NH72 | Trypanosoma rangeli | 30% | 100% |
A4I367 | Leishmania infantum | 72% | 100% |
D0A619 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ADD0 | Leishmania major | 73% | 100% |
E9AZ55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |