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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ARH1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.437 |
DEG_APCC_KENBOX_2 | 49 | 53 | PF00400 | 0.449 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.485 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.471 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.462 |
DOC_PP1_RVXF_1 | 54 | 60 | PF00149 | 0.473 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.409 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 178 | 187 | PF00928 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 231 | 241 | PF00928 | 0.411 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.463 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.167 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.577 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.559 |
LIG_NRP_CendR_1 | 387 | 389 | PF00754 | 0.649 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.281 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.356 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.477 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.323 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.365 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.302 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 351 | 357 | PF11976 | 0.451 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.442 |
MOD_CDK_SPxK_1 | 100 | 106 | PF00069 | 0.437 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.544 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.325 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.360 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.508 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.404 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.457 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.589 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.696 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.341 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.360 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.360 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.605 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.547 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.605 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.652 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.665 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.401 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.582 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.516 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.273 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.348 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.145 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.571 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.675 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.736 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.524 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.659 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.699 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.518 |
MOD_OFUCOSY | 156 | 163 | PF10250 | 0.351 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.469 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.727 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.210 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.615 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.622 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.527 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.477 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.568 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.266 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.587 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.461 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.517 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.678 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.457 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.555 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P400 | Leptomonas seymouri | 60% | 92% |
A0A1X0P6R6 | Trypanosomatidae | 45% | 100% |
A0A3Q8IAW5 | Leishmania donovani | 92% | 100% |
A0A422NWL4 | Trypanosoma rangeli | 42% | 100% |
A4H9D8 | Leishmania braziliensis | 79% | 100% |
A4HXQ9 | Leishmania infantum | 92% | 100% |
B6DTF3 | Bodo saltans | 31% | 100% |
D0A041 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QE08 | Leishmania major | 93% | 100% |
V5DN00 | Trypanosoma cruzi | 40% | 100% |