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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H5E8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 10 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 10 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:0008270 | zinc ion binding | 6 | 4 |
GO:0046914 | transition metal ion binding | 5 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 266 | 270 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.479 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 347 | 353 | PF00134 | 0.650 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.471 |
DOC_MAPK_NFAT4_5 | 342 | 350 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.616 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.490 |
DOC_SPAK_OSR1_1 | 36 | 40 | PF12202 | 0.398 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 298 | 302 | PF12436 | 0.316 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.327 |
LIG_14-3-3_CanoR_1 | 144 | 148 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.469 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.463 |
LIG_Clathr_ClatBox_1 | 239 | 243 | PF01394 | 0.449 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.550 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.403 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.427 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.356 |
LIG_LIR_Gen_1 | 174 | 185 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 234 | 242 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.467 |
LIG_NRBOX | 68 | 74 | PF00104 | 0.484 |
LIG_PALB2_WD40_1 | 299 | 307 | PF16756 | 0.195 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.321 |
LIG_REV1ctd_RIR_1 | 73 | 82 | PF16727 | 0.466 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.404 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.516 |
LIG_SH2_GRB2like | 89 | 92 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.433 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.310 |
LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 237 | 243 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.456 |
LIG_TYR_ITIM | 226 | 231 | PF00017 | 0.472 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.408 |
LIG_UBA3_1 | 239 | 246 | PF00899 | 0.582 |
MOD_CDK_SPxxK_3 | 112 | 119 | PF00069 | 0.317 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.372 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.466 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.587 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.394 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.498 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.498 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.705 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.506 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.398 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.295 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.525 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.533 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.555 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.443 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.671 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.406 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.332 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.544 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.413 |
MOD_N-GLC_2 | 145 | 147 | PF02516 | 0.574 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.392 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.607 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.302 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.455 |
MOD_NEK2_2 | 291 | 296 | PF00069 | 0.265 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.456 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.538 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.482 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.362 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.335 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.485 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.359 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.643 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.549 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.434 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.434 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.321 |
MOD_SUMO_rev_2 | 100 | 109 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 152 | 161 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 355 | 363 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_4 | 253 | 259 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H3 | Leptomonas seymouri | 42% | 97% |
A0A0S4KHN3 | Bodo saltans | 27% | 68% |
A0A1X0NP60 | Trypanosomatidae | 32% | 80% |
A0A3S7WQF3 | Leishmania donovani | 70% | 100% |
C9ZPE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 80% |
E9ACQ5 | Leishmania major | 70% | 100% |
E9AG87 | Leishmania infantum | 71% | 100% |
E9AMH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |