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: A4HI34
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.495 |
CLV_PCSK_FUR_1 | 250 | 254 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.822 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.784 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.822 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.820 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.790 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.845 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.716 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.842 |
DEG_SCF_FBW7_2 | 3 | 9 | PF00400 | 0.801 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.800 |
DOC_CYCLIN_RxL_1 | 12 | 22 | PF00134 | 0.790 |
DOC_MAPK_gen_1 | 210 | 217 | PF00069 | 0.693 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.856 |
DOC_USP7_MATH_2 | 162 | 168 | PF00917 | 0.827 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.847 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.843 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.816 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 32 | 39 | PF00244 | 0.825 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.840 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.801 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.856 |
LIG_CtBP_PxDLS_1 | 64 | 68 | PF00389 | 0.839 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.816 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.762 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.686 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.754 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.787 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.790 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.846 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.713 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.848 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.690 |
LIG_PDZ_Class_2 | 252 | 257 | PF00595 | 0.795 |
LIG_SH2_STAT3 | 224 | 227 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.728 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.793 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.849 |
LIG_SUMO_SIM_anti_2 | 204 | 210 | PF11976 | 0.712 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.568 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.846 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.756 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.808 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.834 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.792 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.836 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.814 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.496 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.845 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.441 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.440 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.835 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.830 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.816 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.843 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.705 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.761 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.691 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.706 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.850 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.847 |
MOD_LATS_1 | 183 | 189 | PF00433 | 0.763 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.697 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.816 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.694 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.580 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.857 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.822 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.827 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.710 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.822 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.842 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.695 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.826 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.704 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.846 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.601 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.809 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.842 |
MOD_SUMO_for_1 | 251 | 254 | PF00179 | 0.780 |
TRG_DiLeu_BaEn_1 | 204 | 209 | PF01217 | 0.712 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.786 |
TRG_DiLeu_BaEn_4 | 204 | 210 | PF01217 | 0.712 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.688 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.707 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.729 |