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: A0A3S7WQF3
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 | 0.626 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.447 |
CLV_PCSK_FUR_1 | 9 | 13 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.482 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.640 |
DOC_SPAK_OSR1_1 | 32 | 36 | PF12202 | 0.399 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.570 |
DOC_USP7_MATH_2 | 255 | 261 | PF00917 | 0.397 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.316 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.446 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.492 |
LIG_Clathr_ClatBox_1 | 235 | 239 | PF01394 | 0.439 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.570 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.382 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.596 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.368 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.702 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 230 | 238 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 301 | 309 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.303 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.377 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.375 |
LIG_REV1ctd_RIR_1 | 69 | 77 | PF16727 | 0.470 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.432 |
LIG_SH2_GRB2like | 85 | 88 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.441 |
LIG_SH3_1 | 192 | 198 | PF00018 | 0.435 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.557 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.562 |
LIG_SH3_4 | 330 | 337 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 64 | 69 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 233 | 239 | PF11976 | 0.535 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.486 |
LIG_UBA3_1 | 235 | 242 | PF00899 | 0.572 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.545 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.425 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.617 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.394 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.581 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.491 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.691 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.578 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.447 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.480 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.508 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.565 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.297 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.638 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.728 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.576 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.406 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.437 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.422 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.351 |
MOD_N-GLC_2 | 141 | 143 | PF02516 | 0.441 |
MOD_N-GLC_2 | 280 | 282 | PF02516 | 0.335 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.548 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.608 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.305 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.596 |
MOD_OFUCOSY | 168 | 175 | PF10250 | 0.393 |
MOD_OFUCOSY | 262 | 269 | PF10250 | 0.421 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.394 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.749 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.469 |
MOD_PK_1 | 348 | 354 | PF00069 | 0.570 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.477 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.483 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.516 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.352 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.516 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 151 | 157 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 96 | 105 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 90 | 95 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_4 | 249 | 255 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H3 | Leptomonas seymouri | 43% | 96% |
A0A0S4KHN3 | Bodo saltans | 27% | 67% |
A0A1X0NP60 | Trypanosomatidae | 31% | 79% |
A4H5E8 | Leishmania braziliensis | 70% | 100% |
C9ZPE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 79% |
E9ACQ5 | Leishmania major | 93% | 100% |
E9AG87 | Leishmania infantum | 98% | 100% |
E9AMH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |