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: Q4QCE2
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 | 0.406 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.249 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.294 |
DOC_CDC14_PxL_1 | 107 | 115 | PF14671 | 0.282 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.339 |
DOC_MAPK_gen_1 | 175 | 182 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 209 | 219 | PF00069 | 0.279 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.316 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.349 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.403 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.352 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.597 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.271 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.280 |
LIG_CaM_IQ_9 | 3 | 19 | PF13499 | 0.390 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.262 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.254 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.396 |
LIG_LIR_Gen_1 | 168 | 173 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 309 | 317 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.310 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.295 |
LIG_REV1ctd_RIR_1 | 205 | 209 | PF16727 | 0.275 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.374 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.455 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.308 |
LIG_SUMO_SIM_par_1 | 177 | 184 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.334 |
LIG_UBA3_1 | 203 | 209 | PF00899 | 0.287 |
LIG_UBA3_1 | 326 | 335 | PF00899 | 0.545 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.484 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.545 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.448 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.345 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.276 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.296 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.301 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.435 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.413 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.409 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.333 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.317 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.356 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.302 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.513 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.441 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.435 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.362 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.323 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.558 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.299 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.483 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.491 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.323 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.294 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.447 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.421 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.292 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.393 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.511 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.415 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.439 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.384 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.262 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.583 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.373 |
MOD_SUMO_for_1 | 364 | 367 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.279 |
TRG_NLS_Bipartite_1 | 344 | 366 | PF00514 | 0.386 |
TRG_NLS_MonoExtC_3 | 360 | 365 | PF00514 | 0.568 |
TRG_NLS_MonoExtN_4 | 361 | 366 | PF00514 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0U9 | Leptomonas seymouri | 58% | 77% |
A0A0S4JCB2 | Bodo saltans | 45% | 98% |
A0A1X0NY04 | Trypanosomatidae | 44% | 100% |
A0A3Q8IAU3 | Leishmania donovani | 93% | 99% |
A0A3R7KMU3 | Trypanosoma rangeli | 48% | 100% |
A4HBR8 | Leishmania braziliensis | 83% | 99% |
A4HZ72 | Leishmania infantum | 92% | 99% |
D0A1G6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AV39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
V5BIF1 | Trypanosoma cruzi | 46% | 100% |