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: E9AMH9
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 | 336 | 340 | PF00656 | 0.758 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.412 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.638 |
DOC_MAPK_HePTP_8 | 81 | 93 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 84 | 93 | PF00069 | 0.297 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.687 |
DOC_SPAK_OSR1_1 | 32 | 36 | PF12202 | 0.545 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.380 |
LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.265 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.500 |
LIG_Clathr_ClatBox_1 | 235 | 239 | PF01394 | 0.509 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.588 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.498 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.472 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.739 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.506 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 213 | 224 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 230 | 238 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 301 | 309 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 316 | 323 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.433 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.518 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.430 |
LIG_REV1ctd_RIR_1 | 69 | 78 | PF16727 | 0.523 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.460 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 85 | 88 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.573 |
LIG_SH3_1 | 192 | 198 | PF00018 | 0.550 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.631 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.601 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.623 |
LIG_SUMO_SIM_anti_2 | 64 | 69 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 90 | 96 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 233 | 239 | PF11976 | 0.595 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.323 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.524 |
LIG_UBA3_1 | 235 | 242 | PF00899 | 0.624 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.512 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.637 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.579 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.443 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.645 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.640 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.711 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.589 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.540 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.558 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.386 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.569 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.476 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.714 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.682 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.471 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.510 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.585 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.455 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.480 |
MOD_N-GLC_2 | 141 | 143 | PF02516 | 0.571 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.565 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.695 |
MOD_OFUCOSY | 168 | 175 | PF10250 | 0.505 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.475 |
MOD_PK_1 | 348 | 354 | PF00069 | 0.681 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.541 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.400 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.541 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.562 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.224 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.469 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.500 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.505 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.458 |
MOD_Plk_2-3 | 322 | 328 | PF00069 | 0.532 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.508 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.458 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.380 |
MOD_SUMO_rev_2 | 148 | 157 | PF00179 | 0.636 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.682 |
MOD_SUMO_rev_2 | 96 | 105 | PF00179 | 0.560 |
TRG_DiLeu_BaEn_1 | 90 | 95 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_4 | 249 | 255 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.429 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H3 | Leptomonas seymouri | 43% | 96% |
A0A0S4KHN3 | Bodo saltans | 27% | 67% |
A0A1X0NP60 | Trypanosomatidae | 30% | 79% |
A0A3S7WQF3 | Leishmania donovani | 87% | 100% |
A4H5E8 | Leishmania braziliensis | 69% | 100% |
C9ZPE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 79% |
E9ACQ5 | Leishmania major | 87% | 100% |
E9AG87 | Leishmania infantum | 88% | 100% |