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: A4H582
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 | 25 | 29 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 481 | 485 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.338 |
CLV_Separin_Metazoa | 446 | 450 | PF03568 | 0.459 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.512 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.363 |
DOC_AGCK_PIF_2 | 202 | 207 | PF00069 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 196 | 202 | PF00134 | 0.605 |
DOC_MAPK_gen_1 | 396 | 403 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 88 | 96 | PF00069 | 0.598 |
DOC_MAPK_RevD_3 | 350 | 363 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 217 | 223 | PF00149 | 0.658 |
DOC_PP1_RVXF_1 | 432 | 439 | PF00149 | 0.482 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.678 |
DOC_USP7_MATH_2 | 463 | 469 | PF00917 | 0.664 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.797 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.621 |
LIG_Actin_RPEL_3 | 391 | 410 | PF02755 | 0.421 |
LIG_Actin_WH2_2 | 235 | 251 | PF00022 | 0.261 |
LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.517 |
LIG_AP_GAE_1 | 490 | 496 | PF02883 | 0.709 |
LIG_APCC_ABBAyCdc20_2 | 456 | 462 | PF00400 | 0.538 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.236 |
LIG_Clathr_ClatBox_1 | 13 | 17 | PF01394 | 0.617 |
LIG_deltaCOP1_diTrp_1 | 473 | 482 | PF00928 | 0.537 |
LIG_EH1_1 | 398 | 406 | PF00400 | 0.546 |
LIG_eIF4E_1 | 372 | 378 | PF01652 | 0.566 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.541 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.506 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.671 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.653 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.473 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.454 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.309 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.289 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.654 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.672 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.632 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.769 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.678 |
LIG_GBD_Chelix_1 | 360 | 368 | PF00786 | 0.436 |
LIG_IBAR_NPY_1 | 252 | 254 | PF08397 | 0.359 |
LIG_IRF3_LxIS_1 | 104 | 109 | PF10401 | 0.567 |
LIG_LIR_Apic_2 | 206 | 210 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 267 | 278 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.469 |
LIG_LIR_LC3C_4 | 269 | 273 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.541 |
LIG_MYND_1 | 74 | 78 | PF01753 | 0.702 |
LIG_MYND_3 | 442 | 446 | PF01753 | 0.465 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.659 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.546 |
LIG_REV1ctd_RIR_1 | 413 | 419 | PF16727 | 0.482 |
LIG_SH2_CRK | 418 | 422 | PF00017 | 0.416 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.613 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.727 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.554 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.703 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.328 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.396 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.482 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.522 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.544 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.638 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.707 |
LIG_SH3_5 | 203 | 207 | PF00018 | 0.606 |
LIG_SUMO_SIM_anti_2 | 374 | 380 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 104 | 109 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 241 | 246 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 402 | 408 | PF11976 | 0.546 |
MOD_CDK_SPK_2 | 106 | 111 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 152 | 159 | PF00069 | 0.622 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.586 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.702 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.675 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.672 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.421 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.508 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.728 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.728 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.639 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.482 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.606 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.680 |
MOD_DYRK1A_RPxSP_1 | 172 | 176 | PF00069 | 0.621 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.543 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.497 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.725 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.589 |
MOD_GlcNHglycan | 33 | 37 | PF01048 | 0.489 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.598 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.327 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.380 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.487 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.447 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.488 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.588 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.728 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.812 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.657 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.724 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.418 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.443 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.543 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.622 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.708 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.648 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.631 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.264 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.321 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.482 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.482 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.482 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.606 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.613 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.357 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.405 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.615 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.621 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.627 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.600 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.622 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.644 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.618 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.338 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.705 |
MOD_Plk_2-3 | 465 | 471 | PF00069 | 0.606 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.570 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.556 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.675 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.373 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.459 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.330 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.603 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.664 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.719 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.506 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.376 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.286 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.724 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.645 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.794 |
MOD_SUMO_rev_2 | 425 | 432 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_4 | 464 | 470 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.691 |
TRG_NES_CRM1_1 | 311 | 326 | PF08389 | 0.392 |
TRG_NES_CRM1_1 | 402 | 413 | PF08389 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I406 | Leptomonas seymouri | 46% | 100% |
A0A3S5H631 | Leishmania donovani | 68% | 99% |
A4HTG6 | Leishmania infantum | 68% | 100% |
E9AM94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QIF4 | Leishmania major | 69% | 99% |