| 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: A4IBC8
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.767 | 
| CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.819 | 
| CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.505 | 
| CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.610 | 
| CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.728 | 
| CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.764 | 
| CLV_PCSK_FUR_1 | 33 | 37 | PF00082 | 0.710 | 
| CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.765 | 
| CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.797 | 
| CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.709 | 
| CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.613 | 
| CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.779 | 
| CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.747 | 
| CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.764 | 
| CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.843 | 
| CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.613 | 
| CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.779 | 
| CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.747 | 
| CLV_PCSK_PC7_1 | 37 | 43 | PF00082 | 0.677 | 
| CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.756 | 
| CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.653 | 
| CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.632 | 
| CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.596 | 
| CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.611 | 
| CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.821 | 
| CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.663 | 
| DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.617 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.814 | 
| DEG_SCF_FBW7_1 | 184 | 191 | PF00400 | 0.698 | 
| DOC_CDC14_PxL_1 | 284 | 292 | PF14671 | 0.562 | 
| DOC_CKS1_1 | 180 | 185 | PF01111 | 0.701 | 
| DOC_CKS1_1 | 220 | 225 | PF01111 | 0.772 | 
| DOC_CKS1_1 | 83 | 88 | PF01111 | 0.768 | 
| DOC_MAPK_gen_1 | 265 | 271 | PF00069 | 0.611 | 
| DOC_MAPK_MEF2A_6 | 236 | 243 | PF00069 | 0.430 | 
| DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.617 | 
| DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.658 | 
| DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.720 | 
| DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.723 | 
| DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.546 | 
| DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.724 | 
| DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.839 | 
| DOC_USP7_UBL2_3 | 35 | 39 | PF12436 | 0.801 | 
| DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.754 | 
| DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.684 | 
| DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.701 | 
| DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.768 | 
| DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.691 | 
| DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.820 | 
| DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.681 | 
| DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.724 | 
| LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.808 | 
| LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.825 | 
| LIG_14-3-3_CanoR_1 | 252 | 262 | PF00244 | 0.535 | 
| LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.541 | 
| LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.669 | 
| LIG_FHA_1 | 189 | 195 | PF00498 | 0.816 | 
| LIG_FHA_1 | 220 | 226 | PF00498 | 0.778 | 
| LIG_FHA_1 | 238 | 244 | PF00498 | 0.321 | 
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.631 | 
| LIG_FHA_1 | 85 | 91 | PF00498 | 0.704 | 
| LIG_FHA_2 | 258 | 264 | PF00498 | 0.561 | 
| LIG_Integrin_isoDGR_2 | 293 | 295 | PF01839 | 0.675 | 
| LIG_Integrin_RGD_1 | 236 | 238 | PF01839 | 0.491 | 
| LIG_LIR_Apic_2 | 313 | 319 | PF02991 | 0.590 | 
| LIG_RPA_C_Fungi | 200 | 212 | PF08784 | 0.641 | 
| LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.726 | 
| LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.464 | 
| LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.456 | 
| LIG_SH3_1 | 211 | 217 | PF00018 | 0.714 | 
| LIG_SH3_1 | 80 | 86 | PF00018 | 0.707 | 
| LIG_SH3_1 | 88 | 94 | PF00018 | 0.674 | 
| LIG_SH3_2 | 185 | 190 | PF14604 | 0.798 | 
| LIG_SH3_2 | 83 | 88 | PF14604 | 0.834 | 
| LIG_SH3_3 | 177 | 183 | PF00018 | 0.820 | 
| LIG_SH3_3 | 211 | 217 | PF00018 | 0.792 | 
| LIG_SH3_3 | 268 | 274 | PF00018 | 0.552 | 
| LIG_SH3_3 | 282 | 288 | PF00018 | 0.690 | 
| LIG_SH3_3 | 45 | 51 | PF00018 | 0.781 | 
| LIG_SH3_3 | 80 | 86 | PF00018 | 0.804 | 
| LIG_SH3_3 | 88 | 94 | PF00018 | 0.733 | 
| LIG_SUMO_SIM_anti_2 | 238 | 243 | PF11976 | 0.565 | 
| LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.489 | 
| MOD_CDK_SPK_2 | 184 | 189 | PF00069 | 0.700 | 
| MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.698 | 
| MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.766 | 
| MOD_CK1_1 | 157 | 163 | PF00069 | 0.708 | 
| MOD_CK1_1 | 257 | 263 | PF00069 | 0.491 | 
| MOD_CK1_1 | 280 | 286 | PF00069 | 0.609 | 
| MOD_CK1_1 | 310 | 316 | PF00069 | 0.521 | 
| MOD_CK1_1 | 72 | 78 | PF00069 | 0.698 | 
| MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.730 | 
| MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.728 | 
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.562 | 
| MOD_GSK3_1 | 184 | 191 | PF00069 | 0.698 | 
| MOD_GSK3_1 | 242 | 249 | PF00069 | 0.577 | 
| MOD_GSK3_1 | 253 | 260 | PF00069 | 0.387 | 
| MOD_GSK3_1 | 273 | 280 | PF00069 | 0.588 | 
| MOD_GSK3_1 | 307 | 314 | PF00069 | 0.549 | 
| MOD_GSK3_1 | 31 | 38 | PF00069 | 0.716 | 
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.707 | 
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.599 | 
| MOD_GSK3_1 | 78 | 85 | PF00069 | 0.642 | 
| MOD_GSK3_1 | 89 | 96 | PF00069 | 0.567 | 
| MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.541 | 
| MOD_NEK2_1 | 242 | 247 | PF00069 | 0.616 | 
| MOD_NEK2_2 | 311 | 316 | PF00069 | 0.533 | 
| MOD_PKA_1 | 110 | 116 | PF00069 | 0.714 | 
| MOD_PKA_1 | 35 | 41 | PF00069 | 0.728 | 
| MOD_PKA_1 | 61 | 67 | PF00069 | 0.648 | 
| MOD_PKA_2 | 109 | 115 | PF00069 | 0.827 | 
| MOD_PKA_2 | 141 | 147 | PF00069 | 0.708 | 
| MOD_PKA_2 | 188 | 194 | PF00069 | 0.824 | 
| MOD_PKA_2 | 307 | 313 | PF00069 | 0.553 | 
| MOD_PKA_2 | 35 | 41 | PF00069 | 0.728 | 
| MOD_PKB_1 | 108 | 116 | PF00069 | 0.715 | 
| MOD_Plk_1 | 237 | 243 | PF00069 | 0.615 | 
| MOD_Plk_1 | 257 | 263 | PF00069 | 0.277 | 
| MOD_Plk_1 | 311 | 317 | PF00069 | 0.528 | 
| MOD_Plk_4 | 196 | 202 | PF00069 | 0.817 | 
| MOD_Plk_4 | 237 | 243 | PF00069 | 0.495 | 
| MOD_Plk_4 | 257 | 263 | PF00069 | 0.358 | 
| MOD_Plk_4 | 280 | 286 | PF00069 | 0.648 | 
| MOD_Plk_4 | 311 | 317 | PF00069 | 0.606 | 
| MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.686 | 
| MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.702 | 
| MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.771 | 
| MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.694 | 
| MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.821 | 
| MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.681 | 
| MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.726 | 
| MOD_SUMO_for_1 | 1 | 4 | PF00179 | 0.697 | 
| TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.745 | 
| TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.740 | 
| TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.674 | 
| TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.610 | 
| TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.690 | 
| TRG_NLS_MonoExtC_3 | 264 | 270 | PF00514 | 0.599 | 
| TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.720 | 
| TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.714 | 
| TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.611 | 
| TRG_Pf-PMV_PEXEL_1 | 295 | 300 | PF00026 | 0.644 | 
| TRG_Pf-PMV_PEXEL_1 | 8 | 13 | PF00026 | 0.543 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A3Q8IF70 | Leishmania donovani | 97% | 99% | 
| A4HMT0 | Leishmania braziliensis | 60% | 90% | 
| E9AF84 | Leishmania major | 88% | 100% | 
| E9B6D9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |