| 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: E9AGC8
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.679 |
| CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.740 |
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.610 |
| CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.663 |
| CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.663 |
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.796 |
| CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.828 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.703 |
| DEG_ODPH_VHL_1 | 176 | 188 | PF01847 | 0.729 |
| DEG_SCF_FBW7_1 | 396 | 402 | PF00400 | 0.712 |
| DEG_SCF_FBW7_2 | 348 | 355 | PF00400 | 0.745 |
| DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.766 |
| DOC_CKS1_1 | 305 | 310 | PF01111 | 0.706 |
| DOC_CKS1_1 | 396 | 401 | PF01111 | 0.714 |
| DOC_CYCLIN_yCln2_LP_2 | 388 | 394 | PF00134 | 0.757 |
| DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.739 |
| DOC_PP4_FxxP_1 | 106 | 109 | PF00568 | 0.741 |
| DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.700 |
| DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.766 |
| DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.761 |
| DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.731 |
| DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.756 |
| DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.760 |
| DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.818 |
| DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.835 |
| DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.853 |
| DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.832 |
| DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.823 |
| DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.762 |
| DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.620 |
| DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.604 |
| LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.792 |
| LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.664 |
| LIG_14-3-3_CanoR_1 | 72 | 81 | PF00244 | 0.648 |
| LIG_AP_GAE_1 | 93 | 99 | PF02883 | 0.664 |
| LIG_BIR_III_2 | 282 | 286 | PF00653 | 0.761 |
| LIG_BIR_III_4 | 51 | 55 | PF00653 | 0.661 |
| LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.775 |
| LIG_Clathr_ClatBox_1 | 8 | 12 | PF01394 | 0.709 |
| LIG_EH_1 | 325 | 329 | PF12763 | 0.678 |
| LIG_eIF4E_1 | 180 | 186 | PF01652 | 0.664 |
| LIG_eIF4E_1 | 361 | 367 | PF01652 | 0.594 |
| LIG_FHA_1 | 152 | 158 | PF00498 | 0.638 |
| LIG_FHA_1 | 221 | 227 | PF00498 | 0.651 |
| LIG_FHA_1 | 305 | 311 | PF00498 | 0.754 |
| LIG_FHA_1 | 387 | 393 | PF00498 | 0.759 |
| LIG_FHA_2 | 368 | 374 | PF00498 | 0.784 |
| LIG_FHA_2 | 46 | 52 | PF00498 | 0.647 |
| LIG_IRF3_LxIS_1 | 56 | 63 | PF10401 | 0.758 |
| LIG_LIR_Apic_2 | 105 | 109 | PF02991 | 0.740 |
| LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.742 |
| LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.741 |
| LIG_NRBOX | 4 | 10 | PF00104 | 0.689 |
| LIG_RPA_C_Fungi | 67 | 79 | PF08784 | 0.675 |
| LIG_SH2_CRK | 86 | 90 | PF00017 | 0.640 |
| LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.759 |
| LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.787 |
| LIG_SH3_3 | 130 | 136 | PF00018 | 0.756 |
| LIG_SH3_3 | 227 | 233 | PF00018 | 0.735 |
| LIG_SH3_3 | 302 | 308 | PF00018 | 0.839 |
| LIG_SH3_3 | 318 | 324 | PF00018 | 0.560 |
| LIG_SUMO_SIM_anti_2 | 181 | 190 | PF11976 | 0.722 |
| LIG_SUMO_SIM_par_1 | 153 | 158 | PF11976 | 0.735 |
| LIG_SUMO_SIM_par_1 | 181 | 190 | PF11976 | 0.722 |
| LIG_SUMO_SIM_par_1 | 365 | 371 | PF11976 | 0.700 |
| LIG_SUMO_SIM_par_1 | 6 | 12 | PF11976 | 0.704 |
| LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.739 |
| LIG_WW_3 | 79 | 83 | PF00397 | 0.742 |
| MOD_CDC14_SPxK_1 | 200 | 203 | PF00782 | 0.849 |
| MOD_CDK_SPK_2 | 85 | 90 | PF00069 | 0.686 |
| MOD_CDK_SPxK_1 | 197 | 203 | PF00069 | 0.839 |
| MOD_CDK_SPxK_1 | 395 | 401 | PF00069 | 0.618 |
| MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.615 |
| MOD_CK1_1 | 135 | 141 | PF00069 | 0.782 |
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.818 |
| MOD_CK1_1 | 199 | 205 | PF00069 | 0.730 |
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.716 |
| MOD_CK2_1 | 122 | 128 | PF00069 | 0.737 |
| MOD_CK2_1 | 266 | 272 | PF00069 | 0.681 |
| MOD_CK2_1 | 70 | 76 | PF00069 | 0.798 |
| MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.652 |
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.787 |
| MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.628 |
| MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.767 |
| MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.739 |
| MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.794 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.804 |
| MOD_GSK3_1 | 151 | 158 | PF00069 | 0.661 |
| MOD_GSK3_1 | 168 | 175 | PF00069 | 0.640 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.754 |
| MOD_GSK3_1 | 24 | 31 | PF00069 | 0.708 |
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.724 |
| MOD_GSK3_1 | 382 | 389 | PF00069 | 0.826 |
| MOD_GSK3_1 | 395 | 402 | PF00069 | 0.615 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.779 |
| MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.732 |
| MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.714 |
| MOD_NEK2_1 | 121 | 126 | PF00069 | 0.835 |
| MOD_NEK2_1 | 299 | 304 | PF00069 | 0.843 |
| MOD_NEK2_1 | 328 | 333 | PF00069 | 0.719 |
| MOD_NEK2_1 | 60 | 65 | PF00069 | 0.756 |
| MOD_NEK2_1 | 70 | 75 | PF00069 | 0.631 |
| MOD_NEK2_1 | 92 | 97 | PF00069 | 0.630 |
| MOD_NEK2_2 | 143 | 148 | PF00069 | 0.692 |
| MOD_PIKK_1 | 231 | 237 | PF00454 | 0.773 |
| MOD_PK_1 | 341 | 347 | PF00069 | 0.601 |
| MOD_PKA_2 | 196 | 202 | PF00069 | 0.789 |
| MOD_PKA_2 | 24 | 30 | PF00069 | 0.663 |
| MOD_Plk_1 | 151 | 157 | PF00069 | 0.734 |
| MOD_Plk_1 | 92 | 98 | PF00069 | 0.664 |
| MOD_Plk_4 | 3 | 9 | PF00069 | 0.634 |
| MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.759 |
| MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.758 |
| MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.820 |
| MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.839 |
| MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.855 |
| MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.833 |
| MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.822 |
| MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.765 |
| MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.621 |
| MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.599 |
| TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.797 |
| TRG_DiLeu_LyEn_5 | 181 | 186 | PF01217 | 0.797 |
| TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.734 |
| TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.742 |
| TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.673 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3S5H6K7 | Leishmania donovani | 99% | 100% |
| A4H6V6 | Leishmania braziliensis | 62% | 97% |
| E9ANW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 95% |
| Q4QGQ2 | Leishmania major | 89% | 100% |