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: Q4QIF4
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_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 373 | 381 | PF00400 | 0.574 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.655 |
DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.646 |
DOC_CKS1_1 | 424 | 429 | PF01111 | 0.738 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.756 |
DOC_MAPK_gen_1 | 321 | 328 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.546 |
DOC_MAPK_RevD_3 | 273 | 288 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 143 | 149 | PF00149 | 0.731 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.506 |
DOC_PP1_RVXF_1 | 357 | 364 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.750 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.678 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.806 |
DOC_USP7_MATH_2 | 388 | 394 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.827 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 173 | 177 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 288 | 296 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 400 | 409 | PF00244 | 0.679 |
LIG_Actin_WH2_2 | 360 | 376 | PF00022 | 0.579 |
LIG_AP_GAE_1 | 416 | 422 | PF02883 | 0.794 |
LIG_APCC_ABBAyCdc20_2 | 381 | 387 | PF00400 | 0.604 |
LIG_EH1_1 | 323 | 331 | PF00400 | 0.619 |
LIG_eIF4E_1 | 297 | 303 | PF01652 | 0.636 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.479 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.493 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.482 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.378 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.702 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.598 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.527 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.608 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.794 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.680 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 281 | 289 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.546 |
LIG_NRBOX | 274 | 280 | PF00104 | 0.436 |
LIG_Pex14_1 | 144 | 148 | PF04695 | 0.732 |
LIG_Pex14_2 | 148 | 152 | PF04695 | 0.572 |
LIG_REV1ctd_RIR_1 | 338 | 344 | PF16727 | 0.546 |
LIG_SH2_NCK_1 | 260 | 264 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.598 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.745 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.446 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.546 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.583 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.739 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.797 |
LIG_SUMO_SIM_anti_2 | 270 | 277 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 155 | 161 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 274 | 281 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 327 | 333 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.616 |
LIG_UBA3_1 | 278 | 287 | PF00899 | 0.280 |
MOD_CDK_SPK_2 | 119 | 124 | PF00069 | 0.640 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.755 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.464 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.523 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.399 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.390 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.536 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.714 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.804 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.568 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.546 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.668 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.741 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.677 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.745 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.639 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.706 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.485 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.419 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.522 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.331 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.778 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.763 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.466 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.466 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.573 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.779 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.446 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.684 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.682 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.707 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.696 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.473 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.324 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.795 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.708 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.463 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.438 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.524 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.346 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.411 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.546 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.546 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.546 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.468 |
MOD_PKA_1 | 287 | 293 | PF00069 | 0.682 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.754 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.449 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.682 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.683 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.716 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.411 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.791 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.520 |
MOD_Plk_2-3 | 390 | 396 | PF00069 | 0.668 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.319 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.396 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.430 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.493 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.494 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.630 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.714 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.787 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.737 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.566 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.431 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.769 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.825 |
MOD_SUMO_rev_2 | 350 | 357 | PF00179 | 0.619 |
TRG_DiLeu_BaEn_4 | 389 | 395 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.546 |
TRG_NES_CRM1_1 | 327 | 338 | PF08389 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I406 | Leptomonas seymouri | 51% | 89% |
A0A3S5H631 | Leishmania donovani | 89% | 85% |
A4H582 | Leishmania braziliensis | 69% | 85% |
A4HTG6 | Leishmania infantum | 90% | 88% |
E9AM94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |