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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HBR8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0030163 | protein catabolic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008914 | leucyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016755 | aminoacyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.565 |
CLV_PCSK_FUR_1 | 360 | 364 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.278 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.326 |
DEG_SCF_FBW7_1 | 156 | 163 | PF00400 | 0.290 |
DOC_CDC14_PxL_1 | 107 | 115 | PF14671 | 0.313 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.370 |
DOC_MAPK_gen_1 | 223 | 232 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.382 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.416 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.430 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.377 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.446 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.642 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.614 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.331 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.239 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.312 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.337 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.326 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.353 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.392 |
LIG_MLH1_MIPbox_1 | 339 | 343 | PF16413 | 0.239 |
LIG_MLH1_MIPbox_1 | 50 | 54 | PF16413 | 0.271 |
LIG_MYND_3 | 230 | 234 | PF01753 | 0.361 |
LIG_PCNA_yPIPBox_3 | 175 | 183 | PF02747 | 0.355 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.271 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.312 |
LIG_REV1ctd_RIR_1 | 340 | 347 | PF16727 | 0.304 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.255 |
LIG_SH2_STAT3 | 29 | 32 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.525 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.327 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 96 | 101 | PF11976 | 0.321 |
LIG_UBA3_1 | 218 | 226 | PF00899 | 0.439 |
LIG_UBA3_1 | 326 | 335 | PF00899 | 0.553 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.545 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.312 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.405 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.461 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.354 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.306 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.311 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.323 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.448 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.357 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.365 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.585 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.395 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.471 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.451 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.392 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.351 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.452 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.588 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.324 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.605 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.450 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.517 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.448 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.322 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.465 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.526 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.481 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.527 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.378 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.500 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.436 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.284 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.593 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.327 |
MOD_SUMO_for_1 | 364 | 367 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.331 |
TRG_DiLeu_LyEn_5 | 234 | 239 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.466 |
TRG_NLS_Bipartite_1 | 298 | 312 | PF00514 | 0.323 |
TRG_NLS_MonoCore_2 | 359 | 364 | PF00514 | 0.369 |
TRG_NLS_MonoExtC_3 | 360 | 365 | PF00514 | 0.591 |
TRG_NLS_MonoExtN_4 | 307 | 312 | PF00514 | 0.396 |
TRG_NLS_MonoExtN_4 | 357 | 364 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0U9 | Leptomonas seymouri | 57% | 77% |
A0A0S4JCB2 | Bodo saltans | 44% | 98% |
A0A1X0NY04 | Trypanosomatidae | 42% | 100% |
A0A3Q8IAU3 | Leishmania donovani | 83% | 99% |
A0A3R7KMU3 | Trypanosoma rangeli | 44% | 100% |
A4HZ72 | Leishmania infantum | 83% | 99% |
D0A1G6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AV39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QCE2 | Leishmania major | 83% | 100% |
V5BIF1 | Trypanosoma cruzi | 41% | 100% |