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: A4HGB0
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0051259 | protein complex oligomerization | 6 | 2 |
GO:0051260 | protein homooligomerization | 7 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.790 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.804 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.839 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.839 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.807 |
DEG_SCF_FBW7_2 | 143 | 148 | PF00400 | 0.775 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.799 |
DOC_MAPK_gen_1 | 7 | 17 | PF00069 | 0.840 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.766 |
DOC_PP1_RVXF_1 | 149 | 156 | PF00149 | 0.802 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.549 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.740 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 93 | 102 | PF02991 | 0.549 |
LIG_LIR_LC3C_4 | 112 | 116 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.804 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.549 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.549 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.767 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 160 | 165 | PF11976 | 0.764 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.549 |
MOD_CDK_SPxK_1 | 141 | 147 | PF00069 | 0.776 |
MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.746 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.549 |
MOD_Cter_Amidation | 5 | 8 | PF01082 | 0.847 |
MOD_GlcNHglycan | 11 | 15 | PF01048 | 0.847 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.791 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.549 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.410 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.549 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.790 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.806 |
MOD_PKB_1 | 8 | 16 | PF00069 | 0.841 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.766 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.554 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.549 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.776 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.585 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.753 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.549 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.662 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.804 |