Although predicted to have a multi-helical architecture, the protein is not hydrophobic enough for a membrane protein.. Unique to kinetoplastids, fast-evolving and duplicated multiple times.
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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4HJ76
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.744 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.787 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.787 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.824 |
DEG_SCF_FBW7_1 | 29 | 35 | PF00400 | 0.804 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.805 |
DOC_MAPK_gen_1 | 129 | 137 | PF00069 | 0.839 |
DOC_MAPK_MEF2A_6 | 131 | 139 | PF00069 | 0.843 |
DOC_MAPK_MEF2A_6 | 194 | 201 | PF00069 | 0.698 |
DOC_PP1_SILK_1 | 253 | 258 | PF00149 | 0.592 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.671 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.823 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.869 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.798 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.775 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.800 |
LIG_14-3-3_CanoR_1 | 182 | 190 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.804 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.766 |
LIG_Actin_WH2_2 | 78 | 96 | PF00022 | 0.757 |
LIG_CSL_BTD_1 | 29 | 32 | PF09270 | 0.807 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.651 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.770 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.795 |
LIG_LIR_Apic_2 | 117 | 122 | PF02991 | 0.819 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.565 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.789 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.845 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.816 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.757 |
LIG_SUMO_SIM_anti_2 | 79 | 86 | PF11976 | 0.763 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.796 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.799 |
LIG_TRAF2_1 | 49 | 52 | PF00917 | 0.806 |
LIG_UBA3_1 | 251 | 258 | PF00899 | 0.701 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.798 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.794 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.801 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.801 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.734 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.827 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.649 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.868 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.756 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.785 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.808 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.550 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.672 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.490 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.765 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.801 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.822 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.573 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.461 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.755 |
MOD_OFUCOSY | 205 | 212 | PF10250 | 0.558 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.802 |
MOD_PK_1 | 131 | 137 | PF00069 | 0.842 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.870 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.801 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.790 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.761 |
MOD_PKB_1 | 129 | 137 | PF00069 | 0.839 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.716 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.677 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.690 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.808 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.799 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.783 |
TRG_DiLeu_BaEn_1 | 203 | 208 | PF01217 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.799 |
TRG_NLS_Bipartite_1 | 165 | 184 | PF00514 | 0.783 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.743 |