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: A0A3Q8ICQ8
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 | 0.610 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.326 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.440 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.360 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.684 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.581 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.363 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.479 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 288 | 292 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 96 | 101 | PF00244 | 0.527 |
LIG_Actin_WH2_2 | 436 | 454 | PF00022 | 0.640 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.440 |
LIG_EH1_1 | 102 | 110 | PF00400 | 0.399 |
LIG_EH1_1 | 326 | 334 | PF00400 | 0.480 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.355 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.565 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.514 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.357 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.540 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.440 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.631 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.677 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.541 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 19 | 30 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 99 | 108 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.379 |
LIG_NRBOX | 209 | 215 | PF00104 | 0.317 |
LIG_Pex14_1 | 18 | 22 | PF04695 | 0.438 |
LIG_Pex14_2 | 115 | 119 | PF04695 | 0.449 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.643 |
LIG_Pex14_2 | 466 | 470 | PF04695 | 0.645 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.597 |
LIG_PTB_Apo_2 | 306 | 313 | PF02174 | 0.600 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.533 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.539 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.533 |
LIG_SUMO_SIM_anti_2 | 21 | 27 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 331 | 337 | PF11976 | 0.410 |
LIG_Vh1_VBS_1 | 9 | 27 | PF01044 | 0.349 |
MOD_CDC14_SPxK_1 | 285 | 288 | PF00782 | 0.514 |
MOD_CDK_SPxK_1 | 282 | 288 | PF00069 | 0.503 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.625 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.411 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.700 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.414 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.517 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.652 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.458 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.517 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.614 |
MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.600 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.293 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.378 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.453 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.652 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.641 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.595 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.447 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.436 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.441 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.490 |
MOD_N-GLC_2 | 309 | 311 | PF02516 | 0.490 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.372 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.481 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.626 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.322 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.366 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.222 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.448 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.355 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.576 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.361 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.512 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.615 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.635 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.610 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.435 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.421 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.619 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.328 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.424 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.311 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.467 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.470 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.391 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.429 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.422 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.456 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.586 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.729 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.673 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 150 | 163 | PF08389 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXY2 | Leptomonas seymouri | 43% | 100% |
A0A0S4JTN4 | Bodo saltans | 29% | 100% |
A0A1X0P483 | Trypanosomatidae | 32% | 100% |
A0A3R7NH72 | Trypanosoma rangeli | 33% | 100% |
A4HFS9 | Leishmania braziliensis | 72% | 100% |
A4I367 | Leishmania infantum | 100% | 100% |
D0A619 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ADD0 | Leishmania major | 92% | 100% |
E9AZ55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |