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: E9AYP5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.478 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.803 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.511 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.630 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.523 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.760 |
DOC_MAPK_gen_1 | 321 | 329 | PF00069 | 0.630 |
DOC_PP1_RVXF_1 | 110 | 116 | PF00149 | 0.469 |
DOC_PP1_RVXF_1 | 228 | 235 | PF00149 | 0.485 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.671 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.789 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.548 |
DOC_USP7_MATH_2 | 129 | 135 | PF00917 | 0.507 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.494 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.796 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.648 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.529 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.451 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.763 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.439 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.518 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.533 |
LIG_LIR_Apic_2 | 267 | 273 | PF02991 | 0.764 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 365 | 369 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.287 |
LIG_LYPXL_yS_3 | 366 | 369 | PF13949 | 0.451 |
LIG_PDZ_Class_2 | 379 | 384 | PF00595 | 0.676 |
LIG_PTB_Apo_2 | 310 | 317 | PF02174 | 0.757 |
LIG_PTB_Phospho_1 | 310 | 316 | PF10480 | 0.759 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.456 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 294 | 297 | PF00017 | 0.705 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.585 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.646 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.700 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.630 |
LIG_SUMO_SIM_par_1 | 200 | 205 | PF11976 | 0.657 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.642 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.676 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.670 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.802 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.680 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.612 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.508 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.741 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.557 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.712 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.547 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.752 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.770 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.719 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.526 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.574 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.671 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.429 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.576 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.337 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.764 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.718 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.571 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.673 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.733 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.481 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.441 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.650 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.482 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.559 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.801 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.429 |
MOD_NEK2_2 | 214 | 219 | PF00069 | 0.564 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.561 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.501 |
MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.638 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.660 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.677 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.424 |
MOD_SUMO_for_1 | 36 | 39 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 358 | 363 | PF00179 | 0.477 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.796 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1E9 | Leptomonas seymouri | 72% | 100% |
A0A0S4IIA8 | Bodo saltans | 48% | 93% |
A0A1X0P7H1 | Trypanosomatidae | 53% | 100% |
A0A3Q8IDW7 | Leishmania donovani | 94% | 100% |
A0A422N3I7 | Trypanosoma rangeli | 52% | 100% |
A4HFA8 | Leishmania braziliensis | 85% | 100% |
A4I2I5 | Leishmania infantum | 94% | 100% |
C9ZWZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 88% |
Q4Q8S7 | Leishmania major | 93% | 100% |
V5BC49 | Trypanosoma cruzi | 54% | 100% |