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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000506 | glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex | 3 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0098796 | membrane protein complex | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 7 |
GO:1902494 | catalytic complex | 2 | 7 |
GO:1990234 | transferase complex | 3 | 7 |
Related structures:
AlphaFold database: E9AM94
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 7 |
GO:0006505 | GPI anchor metabolic process | 6 | 7 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 7 |
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006643 | membrane lipid metabolic process | 4 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 7 |
GO:0006664 | glycolipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 7 |
GO:0008654 | phospholipid biosynthetic process | 5 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009247 | glycolipid biosynthetic process | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 7 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 7 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:1903509 | liposaccharide metabolic process | 4 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.603 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.365 |
DEG_APCC_DBOX_1 | 368 | 376 | PF00400 | 0.497 |
DOC_CKS1_1 | 419 | 424 | PF01111 | 0.646 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.673 |
DOC_MAPK_gen_1 | 316 | 323 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 268 | 283 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.629 |
DOC_PP1_RVXF_1 | 246 | 253 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 352 | 359 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.667 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.616 |
DOC_USP7_MATH_2 | 383 | 389 | PF00917 | 0.636 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 24 | 32 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 395 | 404 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 164 | 181 | PF00022 | 0.354 |
LIG_Actin_WH2_2 | 355 | 371 | PF00022 | 0.504 |
LIG_AP_GAE_1 | 411 | 417 | PF02883 | 0.678 |
LIG_APCC_ABBAyCdc20_2 | 376 | 382 | PF00400 | 0.527 |
LIG_EH1_1 | 318 | 326 | PF00400 | 0.516 |
LIG_eIF4E_1 | 292 | 298 | PF01652 | 0.534 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.289 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.418 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.334 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.313 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.359 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.628 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.527 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.490 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.583 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.677 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.613 |
LIG_GBD_Chelix_1 | 280 | 288 | PF00786 | 0.406 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 276 | 284 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.469 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.369 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.630 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.516 |
LIG_REV1ctd_RIR_1 | 333 | 339 | PF16727 | 0.469 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.593 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.403 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.469 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.505 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.644 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 265 | 272 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 294 | 300 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 168 | 173 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 269 | 277 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 322 | 328 | PF11976 | 0.516 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.270 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.682 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.675 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.631 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.396 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.459 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.371 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.688 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.339 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.469 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.596 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.654 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.463 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.610 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.710 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.588 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.317 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.316 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.422 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.493 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.679 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.690 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.429 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.396 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.515 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.690 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.414 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.411 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.676 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.512 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.529 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.668 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.340 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.391 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.376 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.446 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.272 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.314 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.469 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.469 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.469 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.396 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.587 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.584 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.408 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.563 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.584 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.604 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.651 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.331 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.675 |
MOD_Plk_2-3 | 385 | 391 | PF00069 | 0.596 |
MOD_Plk_2-3 | 407 | 413 | PF00069 | 0.593 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.461 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.362 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.433 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.206 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.404 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.369 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.557 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.633 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.653 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.789 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.389 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.533 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.663 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.729 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.697 |
MOD_SUMO_rev_2 | 345 | 352 | PF00179 | 0.516 |
TRG_DiLeu_BaEn_4 | 384 | 390 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.631 |
TRG_NES_CRM1_1 | 322 | 333 | PF08389 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I406 | Leptomonas seymouri | 53% | 88% |
A0A3S5H631 | Leishmania donovani | 87% | 84% |
A4H582 | Leishmania braziliensis | 67% | 100% |
A4HTG6 | Leishmania infantum | 88% | 87% |
Q4QIF4 | Leishmania major | 85% | 100% |