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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
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 | 10 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
Related structures:
AlphaFold database: E9ADD0
Term | Name | Level | Count |
---|---|---|---|
GO:0006066 | alcohol metabolic process | 3 | 9 |
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 9 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 9 |
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006720 | isoprenoid metabolic process | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 2 |
GO:0008300 | isoprenoid catabolic process | 5 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0009056 | catabolic process | 2 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016042 | lipid catabolic process | 4 | 9 |
GO:0016093 | polyprenol metabolic process | 4 | 9 |
GO:0016094 | polyprenol biosynthetic process | 5 | 2 |
GO:0016095 | polyprenol catabolic process | 5 | 9 |
GO:0019348 | dolichol metabolic process | 5 | 9 |
GO:0019408 | dolichol biosynthetic process | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044242 | cellular lipid catabolic process | 4 | 9 |
GO:0044248 | cellular catabolic process | 3 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 9 |
GO:0044281 | small molecule metabolic process | 2 | 9 |
GO:0044282 | small molecule catabolic process | 3 | 9 |
GO:0044283 | small molecule biosynthetic process | 3 | 2 |
GO:0046164 | alcohol catabolic process | 4 | 9 |
GO:0046165 | alcohol biosynthetic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 9 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 9 |
GO:1901575 | organic substance catabolic process | 3 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 9 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 9 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0003865 | 3-oxo-5-alpha-steroid 4-dehydrogenase activity | 5 | 9 |
GO:0016229 | steroid dehydrogenase activity | 3 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 9 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 9 |
GO:0033765 | steroid dehydrogenase activity, acting on the CH-CH group of donors | 4 | 9 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 7 |
GO:0102389 | polyprenol reductase activity | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.599 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.598 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.570 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.668 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 191 | PF00134 | 0.451 |
DOC_MAPK_gen_1 | 218 | 227 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.555 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.369 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.474 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 10 | 19 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 140 | 149 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 209 | 216 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 254 | 262 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 352 | 361 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 409 | 417 | PF00244 | 0.430 |
LIG_Actin_WH2_2 | 21 | 39 | PF00022 | 0.577 |
LIG_Actin_WH2_2 | 279 | 296 | PF00022 | 0.343 |
LIG_Actin_WH2_2 | 485 | 503 | PF00022 | 0.610 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.427 |
LIG_EH1_1 | 151 | 159 | PF00400 | 0.391 |
LIG_EH1_1 | 375 | 383 | PF00400 | 0.485 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.598 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.382 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.553 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.474 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.401 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.320 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.506 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.537 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.535 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.369 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.622 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.659 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.459 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.552 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.572 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 226 | 236 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 414 | 425 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 68 | 79 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.395 |
LIG_PALB2_WD40_1 | 423 | 431 | PF16756 | 0.224 |
LIG_Pex14_1 | 67 | 71 | PF04695 | 0.433 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.602 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.446 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.638 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.416 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.516 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.465 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.586 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 70 | 76 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 181 | 187 | PF11976 | 0.431 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.570 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.429 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.569 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.546 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.662 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.674 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.438 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.424 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.701 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.396 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.458 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.751 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.482 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.392 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.405 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.683 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.544 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.327 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.343 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.492 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.372 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.696 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.506 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.521 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.444 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.602 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.388 |
MOD_N-GLC_2 | 358 | 360 | PF02516 | 0.398 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.413 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.323 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.597 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.687 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.434 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.399 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.344 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.596 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.501 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.637 |
MOD_PKA_1 | 145 | 151 | PF00069 | 0.494 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.565 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.623 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.511 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.435 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.467 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.466 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.498 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.328 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.592 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.405 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.452 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.418 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.455 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.550 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.652 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.775 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.365 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.554 |
TRG_NES_CRM1_1 | 199 | 212 | PF08389 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 470 | 474 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXY2 | Leptomonas seymouri | 42% | 100% |
A0A1X0P483 | Trypanosomatidae | 31% | 100% |
A0A3Q8ICQ8 | Leishmania donovani | 92% | 100% |
A0A3R7NH72 | Trypanosoma rangeli | 34% | 100% |
A4HFS9 | Leishmania braziliensis | 73% | 100% |
A4I367 | Leishmania infantum | 92% | 100% |
D0A619 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AZ55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |