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: 15 |
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 | yes | yes: 6, no: 4 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0017177 | glucosidase II complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HEV5
Term | Name | Level | Count |
---|---|---|---|
GO:0006491 | N-glycan processing | 5 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009100 | glycoprotein metabolic process | 4 | 7 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0016310 | phosphorylation | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.287 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.188 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.503 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.250 |
DOC_CYCLIN_yCln2_LP_2 | 88 | 91 | PF00134 | 0.193 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 460 | 466 | PF00069 | 0.181 |
DOC_PP1_RVXF_1 | 399 | 406 | PF00149 | 0.181 |
DOC_PP2B_LxvP_1 | 372 | 375 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.193 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.237 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.274 |
DOC_USP7_UBL2_3 | 366 | 370 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.250 |
LIG_14-3-3_CanoR_1 | 5 | 13 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.415 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.193 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.209 |
LIG_Clathr_ClatBox_1 | 383 | 387 | PF01394 | 0.181 |
LIG_Clathr_ClatBox_1 | 474 | 478 | PF01394 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 273 | 278 | PF00928 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 92 | 95 | PF00928 | 0.210 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.193 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.376 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.298 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.162 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.214 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.315 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.193 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.602 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.385 |
LIG_HCF-1_HBM_1 | 397 | 400 | PF13415 | 0.181 |
LIG_LIR_Apic_2 | 486 | 492 | PF02991 | 0.193 |
LIG_LIR_Gen_1 | 259 | 265 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 273 | 282 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 417 | 422 | PF02991 | 0.181 |
LIG_LIR_Gen_1 | 440 | 448 | PF02991 | 0.184 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.193 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.285 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.193 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.285 |
LIG_SH2_CRK | 418 | 422 | PF00017 | 0.163 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.193 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.219 |
LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.181 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.183 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.286 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.233 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.259 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.213 |
LIG_SUMO_SIM_anti_2 | 191 | 198 | PF11976 | 0.307 |
LIG_SUMO_SIM_anti_2 | 84 | 90 | PF11976 | 0.193 |
LIG_SUMO_SIM_par_1 | 343 | 350 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 378 | 387 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 473 | 479 | PF11976 | 0.277 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.274 |
LIG_TRAF2_1 | 378 | 381 | PF00917 | 0.337 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.181 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.653 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.512 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.345 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.439 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.504 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.279 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.290 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.392 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.509 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.486 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.370 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.343 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.273 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.492 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.399 |
MOD_GlcNHglycan | 49 | 53 | PF01048 | 0.250 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.197 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.480 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.534 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.272 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.208 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.273 |
MOD_LATS_1 | 186 | 192 | PF00433 | 0.300 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.597 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.529 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.540 |
MOD_N-GLC_2 | 134 | 136 | PF02516 | 0.188 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.560 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.310 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.260 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.193 |
MOD_OFUCOSY | 313 | 320 | PF10250 | 0.375 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.193 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.193 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.405 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.369 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.503 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.398 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.193 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.543 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.316 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.237 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.237 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.299 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.288 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.193 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.462 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.289 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.372 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.250 |
MOD_SUMO_rev_2 | 157 | 162 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 197 | 202 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 221 | 231 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 387 | 393 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_4 | 206 | 212 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.163 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.237 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 460 | 462 | PF00400 | 0.181 |
TRG_NLS_MonoExtN_4 | 366 | 373 | PF00514 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.193 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4ILH9 | Bodo saltans | 33% | 100% |
A0A1X0NSB3 | Trypanosomatidae | 34% | 100% |
A0A3Q8IDT4 | Leishmania donovani | 52% | 100% |
A0A3R7L6D4 | Trypanosoma rangeli | 33% | 100% |
A4I229 | Leishmania infantum | 52% | 100% |
C9ZRX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AY78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
Q4Q994 | Leishmania major | 52% | 100% |
V5DQZ5 | Trypanosoma cruzi | 31% | 100% |