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: 5 |
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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: A4HJU6
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 19 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 19 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 19 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 19 |
GO:0022857 | transmembrane transporter activity | 2 | 19 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 19 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.620 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.300 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.373 |
DOC_MAPK_gen_1 | 154 | 163 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 234 | 243 | PF00069 | 0.364 |
DOC_MAPK_HePTP_8 | 237 | 249 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 129 | 137 | PF00069 | 0.177 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.369 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.208 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 98 | 107 | PF00244 | 0.341 |
LIG_BIR_III_4 | 43 | 47 | PF00653 | 0.487 |
LIG_CtBP_PxDLS_1 | 90 | 94 | PF00389 | 0.344 |
LIG_eIF4E_1 | 211 | 217 | PF01652 | 0.237 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.209 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.318 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.138 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.350 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.240 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.329 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.181 |
LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.138 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.194 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.266 |
LIG_PDZ_Wminus1_1 | 259 | 261 | PF00595 | 0.317 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.292 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.157 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.404 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.465 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 196 | 203 | PF11976 | 0.138 |
LIG_SUMO_SIM_par_1 | 196 | 203 | PF11976 | 0.138 |
LIG_SUMO_SIM_par_1 | 214 | 220 | PF11976 | 0.198 |
LIG_TYR_ITIM | 45 | 50 | PF00017 | 0.495 |
LIG_UBA3_1 | 28 | 33 | PF00899 | 0.502 |
MOD_CDK_SPxK_1 | 21 | 27 | PF00069 | 0.524 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.473 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.237 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.179 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.267 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.420 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.200 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.730 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.142 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.529 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.690 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.546 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.348 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.243 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.254 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.214 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.218 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.484 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.510 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.701 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.507 |
MOD_PK_1 | 15 | 21 | PF00069 | 0.547 |
MOD_PKA_1 | 239 | 245 | PF00069 | 0.138 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.629 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.617 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.235 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.227 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.699 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.259 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.509 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.570 |
MOD_SUMO_rev_2 | 125 | 131 | PF00179 | 0.152 |
MOD_SUMO_rev_2 | 148 | 155 | PF00179 | 0.138 |
TRG_DiLeu_LyEn_5 | 127 | 132 | PF01217 | 0.129 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.121 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E9 | Leptomonas seymouri | 55% | 94% |
A0A0N0P5K7 | Leptomonas seymouri | 37% | 94% |
A0A1X0NR51 | Trypanosomatidae | 53% | 70% |
A0A1X0NSI7 | Trypanosomatidae | 46% | 69% |
A0A3R7LZX6 | Trypanosoma rangeli | 45% | 74% |
A0A3S7X7B0 | Leishmania donovani | 44% | 78% |
A4HGP7 | Leishmania braziliensis | 55% | 74% |
A4I9G1 | Leishmania infantum | 44% | 78% |
D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 66% |
D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 66% |
D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 66% |
D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 68% |
E8NHP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 78% |
O23039 | Arabidopsis thaliana | 33% | 72% |
O81123 | Arabidopsis thaliana | 27% | 74% |
O81850 | Arabidopsis thaliana | 30% | 75% |
Q6L8G0 | Oryza sativa subsp. japonica | 31% | 74% |
Q6L8G1 | Oryza sativa subsp. japonica | 28% | 71% |
Q75HB1 | Oryza sativa subsp. japonica | 29% | 70% |
Q7XLD4 | Oryza sativa subsp. japonica | 32% | 72% |
Q8W245 | Arabidopsis thaliana | 30% | 72% |
Q9FIS2 | Arabidopsis thaliana | 33% | 74% |
V5AWN3 | Trypanosoma cruzi | 46% | 70% |
V5BC34 | Trypanosoma cruzi | 36% | 71% |
V5DCU2 | Trypanosoma cruzi | 53% | 71% |