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: Q4QAZ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.809 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.802 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.802 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.793 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.793 |
CLV_PCSK_PC7_1 | 118 | 124 | PF00082 | 0.799 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.802 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.831 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.794 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.791 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.822 |
DOC_CYCLIN_yClb3_PxF_3 | 113 | 119 | PF00134 | 0.787 |
DOC_MAPK_FxFP_2 | 15 | 18 | PF00069 | 0.782 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.794 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.792 |
DOC_MAPK_HePTP_8 | 98 | 110 | PF00069 | 0.752 |
DOC_MAPK_MEF2A_6 | 101 | 110 | PF00069 | 0.757 |
DOC_PP1_RVXF_1 | 57 | 63 | PF00149 | 0.819 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.780 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.782 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.784 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.825 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.762 |
LIG_14-3-3_CanoR_1 | 105 | 109 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 118 | 125 | PF00244 | 0.574 |
LIG_14-3-3_CterR_2 | 166 | 169 | PF00244 | 0.787 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.772 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.818 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.812 |
LIG_PDZ_Class_1 | 164 | 169 | PF00595 | 0.781 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.767 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.770 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.772 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.744 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.502 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.784 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.758 |
MOD_CDK_SPxxK_3 | 31 | 38 | PF00069 | 0.824 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.526 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.789 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.464 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.744 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.745 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.765 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.777 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.591 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.452 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.793 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.502 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.781 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.559 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.790 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.759 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.815 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.815 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.764 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.761 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.573 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.814 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.766 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.643 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.753 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.777 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.823 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.760 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.818 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.746 |