| 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 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 4 |
| GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AXF6
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.550 |
| CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.728 |
| CLV_PCSK_FUR_1 | 212 | 216 | PF00082 | 0.510 |
| CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.546 |
| CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.531 |
| CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.512 |
| CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.594 |
| CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.692 |
| DEG_SPOP_SBC_1 | 291 | 295 | PF00917 | 0.652 |
| DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.481 |
| DOC_CKS1_1 | 69 | 74 | PF01111 | 0.377 |
| DOC_CYCLIN_yCln2_LP_2 | 117 | 120 | PF00134 | 0.395 |
| DOC_MAPK_gen_1 | 58 | 65 | PF00069 | 0.489 |
| DOC_MAPK_MEF2A_6 | 58 | 67 | PF00069 | 0.403 |
| DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.430 |
| DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.493 |
| DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.578 |
| DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.413 |
| DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.676 |
| DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.432 |
| DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.505 |
| DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.632 |
| DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.762 |
| DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.416 |
| LIG_Actin_WH2_2 | 126 | 144 | PF00022 | 0.411 |
| LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.382 |
| LIG_FHA_1 | 103 | 109 | PF00498 | 0.486 |
| LIG_FHA_1 | 136 | 142 | PF00498 | 0.423 |
| LIG_FHA_1 | 33 | 39 | PF00498 | 0.386 |
| LIG_FHA_1 | 52 | 58 | PF00498 | 0.443 |
| LIG_FHA_2 | 138 | 144 | PF00498 | 0.380 |
| LIG_FHA_2 | 93 | 99 | PF00498 | 0.406 |
| LIG_Integrin_RGD_1 | 4 | 6 | PF01839 | 0.614 |
| LIG_LIR_Apic_2 | 255 | 259 | PF02991 | 0.745 |
| LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.439 |
| LIG_SH2_CRK | 256 | 260 | PF00017 | 0.818 |
| LIG_SH2_GRB2like | 269 | 272 | PF00017 | 0.770 |
| LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.753 |
| LIG_SH2_STAT3 | 272 | 275 | PF00017 | 0.771 |
| LIG_SH2_STAT3 | 33 | 36 | PF00017 | 0.431 |
| LIG_SH3_3 | 217 | 223 | PF00018 | 0.711 |
| LIG_SH3_3 | 226 | 232 | PF00018 | 0.695 |
| LIG_SH3_3 | 235 | 241 | PF00018 | 0.683 |
| LIG_SH3_3 | 257 | 263 | PF00018 | 0.737 |
| LIG_SH3_3 | 278 | 284 | PF00018 | 0.643 |
| LIG_SH3_3 | 66 | 72 | PF00018 | 0.378 |
| LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.484 |
| LIG_WW_1 | 259 | 262 | PF00397 | 0.695 |
| MOD_CK1_1 | 68 | 74 | PF00069 | 0.426 |
| MOD_CK2_1 | 204 | 210 | PF00069 | 0.589 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.725 |
| MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.651 |
| MOD_GlcNHglycan | 155 | 160 | PF01048 | 0.622 |
| MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.583 |
| MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.412 |
| MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.479 |
| MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.549 |
| MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.592 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.630 |
| MOD_GSK3_1 | 47 | 54 | PF00069 | 0.437 |
| MOD_GSK3_1 | 6 | 13 | PF00069 | 0.560 |
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.481 |
| MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.545 |
| MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.484 |
| MOD_NEK2_1 | 135 | 140 | PF00069 | 0.426 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.412 |
| MOD_NEK2_1 | 88 | 93 | PF00069 | 0.467 |
| MOD_PIKK_1 | 32 | 38 | PF00454 | 0.386 |
| MOD_PKA_1 | 214 | 220 | PF00069 | 0.677 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.362 |
| MOD_PKA_2 | 214 | 220 | PF00069 | 0.702 |
| MOD_PKA_2 | 92 | 98 | PF00069 | 0.405 |
| MOD_PKB_1 | 212 | 220 | PF00069 | 0.676 |
| MOD_Plk_1 | 29 | 35 | PF00069 | 0.496 |
| MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.287 |
| MOD_Plk_4 | 22 | 28 | PF00069 | 0.377 |
| MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.636 |
| MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.763 |
| MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.414 |
| TRG_DiLeu_BaEn_1 | 163 | 168 | PF01217 | 0.378 |
| TRG_DiLeu_BaEn_4 | 55 | 61 | PF01217 | 0.413 |
| TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.709 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IN96 | Leishmania donovani | 84% | 100% |
| A4HE13 | Leishmania braziliensis | 51% | 99% |
| A4I1C0 | Leishmania infantum | 84% | 100% |
| Q4QA16 | Leishmania major | 80% | 100% |