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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B306
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.478 |
CLV_PCSK_PC7_1 | 237 | 243 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.533 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.599 |
DOC_CYCLIN_RxL_1 | 312 | 323 | PF00134 | 0.408 |
DOC_MAPK_gen_1 | 241 | 250 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 241 | 249 | PF00069 | 0.369 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.595 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 177 | 181 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 215 | 223 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.483 |
LIG_deltaCOP1_diTrp_1 | 317 | 321 | PF00928 | 0.273 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.609 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.656 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.576 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.416 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.522 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.481 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.525 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.386 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.691 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.647 |
LIG_LIR_Apic_2 | 156 | 160 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.366 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.613 |
LIG_SH3_1 | 298 | 304 | PF00018 | 0.530 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.702 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 12 | 20 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.440 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.505 |
LIG_UBA3_1 | 247 | 253 | PF00899 | 0.411 |
LIG_WW_1 | 89 | 92 | PF00397 | 0.333 |
LIG_WW_3 | 304 | 308 | PF00397 | 0.493 |
MOD_CDC14_SPxK_1 | 174 | 177 | PF00782 | 0.543 |
MOD_CDK_SPxK_1 | 171 | 177 | PF00069 | 0.548 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.535 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.610 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.567 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.534 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.768 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.597 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.685 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.583 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.470 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.657 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.491 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.248 |
MOD_GlcNHglycan | 167 | 172 | PF01048 | 0.723 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.619 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.552 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.672 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.504 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.527 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.558 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.740 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.647 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.588 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.620 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.588 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.669 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.514 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.661 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.692 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.349 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.356 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.629 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.606 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.400 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.532 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.402 |
MOD_OFUCOSY | 6 | 11 | PF10250 | 0.461 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.440 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.612 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.677 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.350 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.593 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.624 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.555 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.342 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.785 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.615 |
MOD_Plk_2-3 | 275 | 281 | PF00069 | 0.489 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.350 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.397 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.559 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.559 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.585 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Y8 | Leptomonas seymouri | 48% | 98% |
A0A3S7X5S5 | Leishmania donovani | 89% | 100% |
A4HKL6 | Leishmania braziliensis | 70% | 98% |
A4I848 | Leishmania infantum | 90% | 100% |
Q4Q550 | Leishmania major | 86% | 100% |