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: E9AVK7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.653 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.559 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.819 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.846 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.819 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.765 |
DOC_ANK_TNKS_1 | 243 | 250 | PF00023 | 0.790 |
DOC_CYCLIN_RxL_1 | 303 | 316 | PF00134 | 0.807 |
DOC_CYCLIN_yCln2_LP_2 | 97 | 103 | PF00134 | 0.757 |
DOC_PP1_RVXF_1 | 307 | 314 | PF00149 | 0.813 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.840 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.749 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.701 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.780 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.844 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.810 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.813 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.762 |
LIG_BIR_III_2 | 316 | 320 | PF00653 | 0.821 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.757 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.843 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.762 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.556 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.757 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.549 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.792 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.662 |
LIG_PDZ_Class_1 | 324 | 329 | PF00595 | 0.650 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.550 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.765 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.530 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.826 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 88 | 96 | PF11976 | 0.613 |
MOD_CDK_SPxxK_3 | 148 | 155 | PF00069 | 0.659 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.843 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.819 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.606 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.756 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.784 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.691 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.808 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.786 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.843 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.710 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.705 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.825 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.638 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.754 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.763 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.543 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.585 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.649 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.757 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.750 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.653 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.580 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.548 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.789 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.756 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.750 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.809 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.811 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.745 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.662 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.704 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.685 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.645 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.762 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.763 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.705 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.829 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.628 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.821 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.559 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.812 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.806 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.814 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.653 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.537 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.541 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.678 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.775 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.812 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.770 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.797 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.534 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.843 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.757 |
MOD_SUMO_rev_2 | 58 | 65 | PF00179 | 0.613 |
TRG_ER_diArg_1 | 54 | 57 | PF00400 | 0.553 |
TRG_NLS_Bipartite_1 | 40 | 57 | PF00514 | 0.555 |
TRG_NLS_MonoExtC_3 | 52 | 58 | PF00514 | 0.738 |
TRG_NLS_MonoExtN_4 | 50 | 57 | PF00514 | 0.740 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7A5 | Leishmania donovani | 80% | 100% |
A4HC74 | Leishmania braziliensis | 55% | 100% |
A4HZQ1 | Leishmania infantum | 80% | 100% |
Q4QBX2 | Leishmania major | 81% | 100% |