| 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: 5 |
| NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B3D4
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.745 |
| CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.653 |
| CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.390 |
| CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.448 |
| CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.547 |
| CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.520 |
| CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.369 |
| DOC_CKS1_1 | 160 | 165 | PF01111 | 0.619 |
| DOC_MAPK_gen_1 | 258 | 266 | PF00069 | 0.610 |
| DOC_MAPK_MEF2A_6 | 258 | 266 | PF00069 | 0.354 |
| DOC_PP4_FxxP_1 | 145 | 148 | PF00568 | 0.574 |
| DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.657 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.638 |
| DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.276 |
| DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.653 |
| DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.338 |
| DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.646 |
| DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.585 |
| DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.614 |
| LIG_14-3-3_CanoR_1 | 149 | 155 | PF00244 | 0.573 |
| LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.422 |
| LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.487 |
| LIG_Actin_WH2_2 | 253 | 270 | PF00022 | 0.308 |
| LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.601 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.510 |
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.565 |
| LIG_FHA_1 | 80 | 86 | PF00498 | 0.456 |
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.413 |
| LIG_FHA_2 | 18 | 24 | PF00498 | 0.584 |
| LIG_FHA_2 | 250 | 256 | PF00498 | 0.337 |
| LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.422 |
| LIG_LIR_Gen_1 | 153 | 161 | PF02991 | 0.587 |
| LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.631 |
| LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.585 |
| LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.560 |
| LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.571 |
| LIG_NRBOX | 156 | 162 | PF00104 | 0.595 |
| LIG_PCNA_yPIPBox_3 | 114 | 128 | PF02747 | 0.400 |
| LIG_Pex14_2 | 49 | 53 | PF04695 | 0.357 |
| LIG_SH2_CRK | 115 | 119 | PF00017 | 0.596 |
| LIG_SH2_CRK | 139 | 143 | PF00017 | 0.451 |
| LIG_SH2_CRK | 218 | 222 | PF00017 | 0.603 |
| LIG_SH2_PTP2 | 154 | 157 | PF00017 | 0.534 |
| LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.515 |
| LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.589 |
| LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.588 |
| LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.660 |
| LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.793 |
| LIG_TYR_ITIM | 152 | 157 | PF00017 | 0.581 |
| LIG_UBA3_1 | 262 | 268 | PF00899 | 0.357 |
| MOD_CK1_1 | 153 | 159 | PF00069 | 0.562 |
| MOD_CK1_1 | 71 | 77 | PF00069 | 0.610 |
| MOD_CK2_1 | 249 | 255 | PF00069 | 0.601 |
| MOD_CK2_1 | 289 | 295 | PF00069 | 0.725 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.627 |
| MOD_GlcNHglycan | 8 | 12 | PF01048 | 0.511 |
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.639 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.544 |
| MOD_GSK3_1 | 47 | 54 | PF00069 | 0.607 |
| MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.356 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.523 |
| MOD_NEK2_1 | 190 | 195 | PF00069 | 0.405 |
| MOD_NEK2_1 | 230 | 235 | PF00069 | 0.553 |
| MOD_NEK2_1 | 249 | 254 | PF00069 | 0.361 |
| MOD_NEK2_1 | 47 | 52 | PF00069 | 0.609 |
| MOD_NEK2_1 | 79 | 84 | PF00069 | 0.582 |
| MOD_NEK2_2 | 9 | 14 | PF00069 | 0.502 |
| MOD_PIKK_1 | 190 | 196 | PF00454 | 0.523 |
| MOD_PKA_1 | 207 | 213 | PF00069 | 0.649 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.753 |
| MOD_PKA_2 | 79 | 85 | PF00069 | 0.467 |
| MOD_Plk_1 | 216 | 222 | PF00069 | 0.354 |
| MOD_Plk_2-3 | 17 | 23 | PF00069 | 0.742 |
| MOD_Plk_4 | 107 | 113 | PF00069 | 0.572 |
| MOD_Plk_4 | 150 | 156 | PF00069 | 0.265 |
| MOD_Plk_4 | 216 | 222 | PF00069 | 0.610 |
| MOD_Plk_4 | 275 | 281 | PF00069 | 0.533 |
| MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.615 |
| MOD_SUMO_rev_2 | 100 | 110 | PF00179 | 0.371 |
| TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.601 |
| TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.588 |
| TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.605 |
| TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.619 |
| TRG_NES_CRM1_1 | 23 | 34 | PF08389 | 0.405 |
| TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.616 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IH56 | Leishmania donovani | 86% | 100% |
| A4HKZ3 | Leishmania braziliensis | 71% | 100% |
| A4I8H4 | Leishmania infantum | 86% | 100% |
| E9AEG9 | Leishmania major | 83% | 66% |