| 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: 3 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 4 |
| 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: A4H824
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0009605 | response to external stimulus | 2 | 1 |
| GO:0009607 | response to biotic stimulus | 2 | 1 |
| GO:0042783 | evasion of host immune response | 6 | 1 |
| GO:0042784 | evasion of host immune response via modulation of host complement system | 7 | 1 |
| GO:0043207 | response to external biotic stimulus | 3 | 1 |
| GO:0044403 | biological process involved in symbiotic interaction | 2 | 1 |
| GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 1 |
| GO:0050896 | response to stimulus | 1 | 1 |
| GO:0051701 | biological process involved in interaction with host | 3 | 1 |
| GO:0051707 | response to other organism | 2 | 1 |
| GO:0052173 | response to defenses of other organism | 3 | 1 |
| GO:0052200 | response to host defenses | 4 | 1 |
| GO:0052572 | response to host immune response | 5 | 1 |
| GO:0075136 | response to host | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0004857 | enzyme inhibitor activity | 3 | 7 |
| GO:0004866 | endopeptidase inhibitor activity | 5 | 7 |
| GO:0004867 | serine-type endopeptidase inhibitor activity | 6 | 7 |
| GO:0030234 | enzyme regulator activity | 2 | 7 |
| GO:0030414 | peptidase inhibitor activity | 4 | 7 |
| GO:0061134 | peptidase regulator activity | 3 | 7 |
| GO:0061135 | endopeptidase regulator activity | 4 | 7 |
| GO:0098772 | molecular function regulator activity | 1 | 7 |
| GO:0140678 | molecular function inhibitor activity | 2 | 7 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.577 |
| CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.614 |
| CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.863 |
| CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.654 |
| CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.750 |
| CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.676 |
| CLV_PCSK_FUR_1 | 257 | 261 | PF00082 | 0.632 |
| CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.311 |
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.340 |
| CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.778 |
| CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.670 |
| CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.700 |
| CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.652 |
| CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.311 |
| CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.311 |
| CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.715 |
| CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.675 |
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.608 |
| CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.650 |
| DEG_SCF_FBW7_1 | 216 | 223 | PF00400 | 0.620 |
| DOC_MAPK_gen_1 | 111 | 118 | PF00069 | 0.311 |
| DOC_MAPK_gen_1 | 19 | 25 | PF00069 | 0.340 |
| DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.479 |
| DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.549 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.461 |
| DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.626 |
| DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.615 |
| DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.817 |
| DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.780 |
| DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.790 |
| DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.814 |
| DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.622 |
| DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.470 |
| DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.578 |
| DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.865 |
| DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.835 |
| DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.757 |
| DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.382 |
| LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.679 |
| LIG_14-3-3_CanoR_1 | 287 | 292 | PF00244 | 0.617 |
| LIG_14-3-3_CterR_2 | 306 | 309 | PF00244 | 0.617 |
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.504 |
| LIG_FHA_2 | 58 | 64 | PF00498 | 0.358 |
| LIG_FHA_2 | 75 | 81 | PF00498 | 0.402 |
| LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.532 |
| LIG_LIR_Apic_2 | 68 | 72 | PF02991 | 0.299 |
| LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.311 |
| LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.447 |
| LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.485 |
| LIG_MYND_3 | 1 | 5 | PF01753 | 0.444 |
| LIG_Pex14_1 | 69 | 73 | PF04695 | 0.403 |
| LIG_SH2_CRK | 7 | 11 | PF00017 | 0.512 |
| LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.656 |
| LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.510 |
| LIG_SH2_STAT3 | 82 | 85 | PF00017 | 0.311 |
| LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.440 |
| LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.461 |
| LIG_SH3_1 | 101 | 107 | PF00018 | 0.311 |
| LIG_SH3_3 | 101 | 107 | PF00018 | 0.407 |
| LIG_SH3_3 | 113 | 119 | PF00018 | 0.389 |
| LIG_SH3_3 | 172 | 178 | PF00018 | 0.570 |
| LIG_SH3_3 | 85 | 91 | PF00018 | 0.348 |
| LIG_SUMO_SIM_par_1 | 168 | 174 | PF11976 | 0.570 |
| LIG_SUMO_SIM_par_1 | 74 | 80 | PF11976 | 0.447 |
| LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.526 |
| MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.860 |
| MOD_CDC14_SPxK_1 | 297 | 300 | PF00782 | 0.757 |
| MOD_CDK_SPK_2 | 212 | 217 | PF00069 | 0.620 |
| MOD_CDK_SPK_2 | 288 | 293 | PF00069 | 0.835 |
| MOD_CDK_SPK_2 | 294 | 299 | PF00069 | 0.757 |
| MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.841 |
| MOD_CK1_1 | 174 | 180 | PF00069 | 0.583 |
| MOD_CK1_1 | 201 | 207 | PF00069 | 0.833 |
| MOD_CK1_1 | 212 | 218 | PF00069 | 0.637 |
| MOD_CK1_1 | 223 | 229 | PF00069 | 0.606 |
| MOD_CK1_1 | 261 | 267 | PF00069 | 0.836 |
| MOD_CK1_1 | 62 | 68 | PF00069 | 0.518 |
| MOD_CK2_1 | 136 | 142 | PF00069 | 0.514 |
| MOD_CK2_1 | 27 | 33 | PF00069 | 0.311 |
| MOD_CK2_1 | 270 | 276 | PF00069 | 0.544 |
| MOD_CK2_1 | 57 | 63 | PF00069 | 0.461 |
| MOD_DYRK1A_RPxSP_1 | 294 | 298 | PF00069 | 0.779 |
| MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.621 |
| MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.834 |
| MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.782 |
| MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.763 |
| MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.638 |
| MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.311 |
| MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.869 |
| MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.774 |
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.588 |
| MOD_GSK3_1 | 196 | 203 | PF00069 | 0.748 |
| MOD_GSK3_1 | 207 | 214 | PF00069 | 0.755 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.672 |
| MOD_GSK3_1 | 239 | 246 | PF00069 | 0.743 |
| MOD_GSK3_1 | 258 | 265 | PF00069 | 0.769 |
| MOD_GSK3_1 | 288 | 295 | PF00069 | 0.739 |
| MOD_GSK3_1 | 298 | 305 | PF00069 | 0.785 |
| MOD_GSK3_1 | 55 | 62 | PF00069 | 0.524 |
| MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.655 |
| MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.670 |
| MOD_NEK2_1 | 190 | 195 | PF00069 | 0.623 |
| MOD_NEK2_1 | 196 | 201 | PF00069 | 0.564 |
| MOD_NEK2_1 | 207 | 212 | PF00069 | 0.581 |
| MOD_NEK2_1 | 57 | 62 | PF00069 | 0.493 |
| MOD_PIKK_1 | 136 | 142 | PF00454 | 0.514 |
| MOD_PIKK_1 | 146 | 152 | PF00454 | 0.531 |
| MOD_PKA_1 | 191 | 197 | PF00069 | 0.713 |
| MOD_PKA_1 | 239 | 245 | PF00069 | 0.866 |
| MOD_PKA_1 | 258 | 264 | PF00069 | 0.585 |
| MOD_PKA_2 | 223 | 229 | PF00069 | 0.761 |
| MOD_PKA_2 | 239 | 245 | PF00069 | 0.816 |
| MOD_PKA_2 | 302 | 308 | PF00069 | 0.803 |
| MOD_PKB_1 | 285 | 293 | PF00069 | 0.607 |
| MOD_Plk_1 | 229 | 235 | PF00069 | 0.623 |
| MOD_Plk_1 | 243 | 249 | PF00069 | 0.553 |
| MOD_Plk_1 | 62 | 68 | PF00069 | 0.461 |
| MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.470 |
| MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.583 |
| MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.865 |
| MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.841 |
| MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.382 |
| MOD_SUMO_rev_2 | 270 | 279 | PF00179 | 0.563 |
| TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.461 |
| TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.892 |
| TRG_NLS_Bipartite_1 | 239 | 261 | PF00514 | 0.864 |
| TRG_NLS_MonoCore_2 | 256 | 261 | PF00514 | 0.629 |
| TRG_NLS_MonoExtC_3 | 256 | 262 | PF00514 | 0.632 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HZ51 | Leptomonas seymouri | 34% | 91% |
| A0A3S7WTD9 | Leishmania donovani | 46% | 82% |
| A4H824 | Leishmania braziliensis | 100% | 100% |
| A4HWF0 | Leishmania infantum | 46% | 82% |
| E9AQ49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 83% |
| Q4QFD3 | Leishmania major | 46% | 100% |