Leucine-rich repeat proteins with a hydrophobic terminal helix. Unlike its distant animal relatives, this cytoplasmic sensor protein might be anchored to the membrane.
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 5 |
GO:0016020 | membrane | 2 | 4 |
GO:0042995 | cell projection | 2 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 5 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B0E0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.624 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.624 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.427 |
DOC_MAPK_gen_1 | 182 | 193 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 4 | 13 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 63 | 71 | PF00069 | 0.627 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.605 |
DOC_USP7_UBL2_3 | 88 | 92 | PF12436 | 0.627 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 4 | 13 | PF00244 | 0.581 |
LIG_14-3-3_CterR_2 | 212 | 216 | PF00244 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.627 |
LIG_DLG_GKlike_1 | 63 | 71 | PF00625 | 0.627 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.688 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.627 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.503 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.581 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.627 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.627 |
LIG_LIR_Apic_2 | 156 | 161 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.627 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.705 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 172 | 176 | PF00017 | 0.645 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.666 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.666 |
LIG_SUMO_SIM_par_1 | 35 | 41 | PF11976 | 0.627 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.518 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.642 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.627 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.685 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.627 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.685 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.545 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.663 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.587 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.589 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.427 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.596 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.598 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.422 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.452 |
MOD_NEK2_2 | 181 | 186 | PF00069 | 0.743 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.674 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.748 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.627 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.627 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.581 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.397 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 183 | 188 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 4 | 8 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X2X2 | Leishmania donovani | 94% | 100% |
A4I510 | Leishmania infantum | 94% | 100% |
Q4Q7T8 | Leishmania major | 92% | 100% |