Protein modification, Lipoate- ligase-like
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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4HTD2
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009249 | protein lipoylation | 5 | 4 |
GO:0018193 | peptidyl-amino acid modification | 5 | 4 |
GO:0018205 | peptidyl-lysine modification | 6 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0036211 | protein modification process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043412 | macromolecule modification | 4 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0051604 | protein maturation | 4 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016874 | ligase activity | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.309 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.255 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.479 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.356 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.351 |
DOC_CYCLIN_RxL_1 | 318 | 325 | PF00134 | 0.197 |
DOC_MIT_MIM_1 | 172 | 180 | PF04212 | 0.237 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.287 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.321 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.318 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.301 |
LIG_14-3-3_CanoR_1 | 148 | 155 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 265 | 272 | PF00244 | 0.221 |
LIG_14-3-3_CanoR_1 | 97 | 101 | PF00244 | 0.272 |
LIG_Clathr_ClatBox_1 | 112 | 116 | PF01394 | 0.332 |
LIG_deltaCOP1_diTrp_1 | 154 | 162 | PF00928 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 325 | 333 | PF00928 | 0.221 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.290 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.264 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.267 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.232 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.347 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.193 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.305 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.396 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.482 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.295 |
LIG_Integrin_RGD_1 | 137 | 139 | PF01839 | 0.368 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.310 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 181 | 189 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 30 | 41 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.287 |
LIG_NRBOX | 266 | 272 | PF00104 | 0.236 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.296 |
LIG_SH2_NCK_1 | 157 | 161 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.268 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.267 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.354 |
LIG_SH3_5 | 29 | 33 | PF00018 | 0.286 |
LIG_SUMO_SIM_anti_2 | 194 | 202 | PF11976 | 0.231 |
LIG_SUMO_SIM_par_1 | 12 | 19 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 163 | 169 | PF11976 | 0.217 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.192 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.260 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.244 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.361 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.263 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.461 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.538 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.328 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.335 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.298 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.245 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.263 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.282 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.277 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.303 |
MOD_Cter_Amidation | 131 | 134 | PF01082 | 0.369 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.228 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.439 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.401 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.194 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.405 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.298 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.472 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.400 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.389 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.316 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.312 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.282 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.296 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.248 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.420 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.255 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.200 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.302 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.279 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.264 |
MOD_PKA_1 | 133 | 139 | PF00069 | 0.385 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.364 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.292 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.269 |
MOD_PKB_1 | 174 | 182 | PF00069 | 0.250 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.295 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.307 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.301 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.274 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.214 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.366 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.250 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.320 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.303 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.291 |
TRG_NES_CRM1_1 | 172 | 185 | PF08389 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 25 | 30 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 321 | 325 | PF00026 | 0.202 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NQ94 | Trypanosomatidae | 30% | 70% |
V5B8E4 | Trypanosoma cruzi | 31% | 100% |