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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: E9B3Z5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 221 | 227 | PF00089 | 0.755 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.650 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.820 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.820 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.700 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.729 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.669 |
DEG_SCF_FBW7_1 | 4 | 11 | PF00400 | 0.709 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.717 |
DOC_CKS1_1 | 60 | 65 | PF01111 | 0.563 |
DOC_CYCLIN_RxL_1 | 104 | 115 | PF00134 | 0.644 |
DOC_CYCLIN_RxL_1 | 19 | 28 | PF00134 | 0.656 |
DOC_MAPK_gen_1 | 29 | 35 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 105 | 112 | PF00149 | 0.637 |
DOC_PP1_RVXF_1 | 32 | 39 | PF00149 | 0.618 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.769 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.703 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.817 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 184 | 192 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 71 | 87 | PF00022 | 0.651 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.681 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.507 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.540 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.711 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.404 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.666 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.776 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.664 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.537 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 54 | 59 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.728 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.743 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.751 |
LIG_LYPXL_yS_3 | 146 | 149 | PF13949 | 0.526 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.665 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.818 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.795 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.528 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.532 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.736 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 136 | 141 | PF11976 | 0.669 |
LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.769 |
LIG_WRC_WIRS_1 | 35 | 40 | PF05994 | 0.643 |
MOD_CDK_SPxK_1 | 59 | 65 | PF00069 | 0.818 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.530 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.598 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.586 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.766 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.646 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.527 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.767 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.648 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.801 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.694 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.705 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.769 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.659 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.661 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.542 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.664 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.682 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.738 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.655 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.728 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.493 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.709 |
MOD_LATS_1 | 160 | 166 | PF00433 | 0.812 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.539 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.541 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.760 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.691 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.718 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.619 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.693 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.541 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.543 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.619 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.749 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.749 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.614 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.763 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.660 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.539 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.707 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.818 |
MOD_SUMO_rev_2 | 110 | 118 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 91 | 95 | PF00179 | 0.683 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.696 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.600 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.729 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.662 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHI6 | Leishmania donovani | 93% | 100% |
A4I930 | Leishmania infantum | 93% | 100% |
Q4Q429 | Leishmania major | 92% | 100% |