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: E9AP38
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.386 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.480 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.458 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.337 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.436 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 136 | 146 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 202 | 208 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 273 | 280 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.511 |
LIG_Actin_WH2_2 | 67 | 84 | PF00022 | 0.355 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.494 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.436 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.560 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.395 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.489 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.646 |
LIG_LIR_Gen_1 | 123 | 132 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.501 |
LIG_PTAP_UEV_1 | 279 | 284 | PF05743 | 0.485 |
LIG_SH2_GRB2like | 151 | 154 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.496 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.444 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.506 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.392 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.542 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.472 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.496 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.636 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.473 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.430 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.503 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.338 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.613 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.497 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.556 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.318 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.544 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.620 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.424 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.618 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.491 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.358 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.387 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.617 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.420 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.524 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.389 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.498 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.348 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.420 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.522 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.552 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.516 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.630 |
MOD_SUMO_rev_2 | 86 | 92 | PF00179 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.482 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2V4 | Leptomonas seymouri | 56% | 92% |
A0A3Q8IBM3 | Leishmania donovani | 87% | 100% |
A4H712 | Leishmania braziliensis | 67% | 100% |
A4HVE0 | Leishmania infantum | 87% | 100% |
Q4QGF0 | Leishmania major | 84% | 100% |