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: Q4QHN9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.834 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.805 |
CLV_PCSK_FUR_1 | 22 | 26 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.834 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.752 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.808 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.755 |
DEG_APCC_DBOX_1 | 52 | 60 | PF00400 | 0.779 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.834 |
DOC_CYCLIN_RxL_1 | 34 | 44 | PF00134 | 0.750 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.757 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.828 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 41 | 50 | PF00244 | 0.761 |
LIG_Clathr_ClatBox_1 | 56 | 60 | PF01394 | 0.786 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.844 |
LIG_LIR_Apic_2 | 38 | 43 | PF02991 | 0.755 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.794 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.828 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.587 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.765 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.779 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.811 |
LIG_SUMO_SIM_par_1 | 55 | 60 | PF11976 | 0.785 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.844 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.793 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.835 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.762 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.815 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.790 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.769 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.840 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.819 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.837 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.796 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.820 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.835 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.814 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.824 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.825 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.642 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.484 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.773 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.829 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.822 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.767 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.833 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.834 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.741 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.834 |
MOD_Plk_2-3 | 10 | 16 | PF00069 | 0.815 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.748 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.792 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.820 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.777 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.814 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.776 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.806 |
TRG_NLS_MonoExtC_3 | 20 | 25 | PF00514 | 0.808 |