| 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: 16 |
| NetGPI | no | yes: 0, no: 16 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 17 |
| GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: Q4Q0S5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 17 |
| GO:0008643 | carbohydrate transport | 5 | 17 |
| GO:0051179 | localization | 1 | 17 |
| GO:0051234 | establishment of localization | 2 | 17 |
| GO:0071702 | organic substance transport | 4 | 17 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 3 |
| GO:0015144 | carbohydrate transmembrane transporter activity | 3 | 3 |
| GO:0022857 | transmembrane transporter activity | 2 | 3 |
| GO:0051119 | sugar transmembrane transporter activity | 4 | 3 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.329 |
| DOC_CYCLIN_yCln2_LP_2 | 152 | 158 | PF00134 | 0.358 |
| DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.251 |
| DOC_MAPK_gen_1 | 31 | 41 | PF00069 | 0.529 |
| DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.529 |
| DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.251 |
| DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.465 |
| DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.316 |
| LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.465 |
| LIG_Actin_WH2_2 | 83 | 101 | PF00022 | 0.459 |
| LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.358 |
| LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.265 |
| LIG_EH1_1 | 114 | 122 | PF00400 | 0.353 |
| LIG_FHA_1 | 107 | 113 | PF00498 | 0.297 |
| LIG_FHA_1 | 228 | 234 | PF00498 | 0.649 |
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.234 |
| LIG_FHA_1 | 59 | 65 | PF00498 | 0.336 |
| LIG_FHA_1 | 99 | 105 | PF00498 | 0.538 |
| LIG_GBD_Chelix_1 | 117 | 125 | PF00786 | 0.359 |
| LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.344 |
| LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.241 |
| LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.343 |
| LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.335 |
| LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.232 |
| LIG_NRBOX | 115 | 121 | PF00104 | 0.292 |
| LIG_NRBOX | 187 | 193 | PF00104 | 0.412 |
| LIG_Pex3_1 | 119 | 130 | PF04882 | 0.278 |
| LIG_SH2_CRK | 189 | 193 | PF00017 | 0.328 |
| LIG_SH2_CRK | 79 | 83 | PF00017 | 0.323 |
| LIG_SH2_PTP2 | 197 | 200 | PF00017 | 0.362 |
| LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.381 |
| LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.513 |
| LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.383 |
| LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.362 |
| LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.313 |
| LIG_SUMO_SIM_par_1 | 190 | 195 | PF11976 | 0.296 |
| LIG_SUMO_SIM_par_1 | 22 | 29 | PF11976 | 0.407 |
| LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.402 |
| MOD_CK1_1 | 106 | 112 | PF00069 | 0.335 |
| MOD_CK1_1 | 129 | 135 | PF00069 | 0.304 |
| MOD_CK1_1 | 23 | 29 | PF00069 | 0.437 |
| MOD_CK1_1 | 35 | 41 | PF00069 | 0.553 |
| MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.385 |
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.489 |
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.311 |
| MOD_GSK3_1 | 19 | 26 | PF00069 | 0.316 |
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.509 |
| MOD_GSK3_1 | 6 | 13 | PF00069 | 0.292 |
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.518 |
| MOD_NEK2_1 | 128 | 133 | PF00069 | 0.344 |
| MOD_NEK2_1 | 150 | 155 | PF00069 | 0.345 |
| MOD_NEK2_1 | 158 | 163 | PF00069 | 0.311 |
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.389 |
| MOD_NEK2_1 | 19 | 24 | PF00069 | 0.362 |
| MOD_NEK2_1 | 196 | 201 | PF00069 | 0.287 |
| MOD_NEK2_1 | 39 | 44 | PF00069 | 0.357 |
| MOD_NEK2_1 | 4 | 9 | PF00069 | 0.319 |
| MOD_NEK2_1 | 98 | 103 | PF00069 | 0.542 |
| MOD_NEK2_2 | 110 | 115 | PF00069 | 0.381 |
| MOD_NEK2_2 | 145 | 150 | PF00069 | 0.334 |
| MOD_Plk_4 | 110 | 116 | PF00069 | 0.361 |
| MOD_Plk_4 | 145 | 151 | PF00069 | 0.294 |
| MOD_Plk_4 | 158 | 164 | PF00069 | 0.273 |
| MOD_Plk_4 | 172 | 178 | PF00069 | 0.360 |
| MOD_Plk_4 | 180 | 186 | PF00069 | 0.335 |
| MOD_Plk_4 | 20 | 26 | PF00069 | 0.401 |
| MOD_Plk_4 | 99 | 105 | PF00069 | 0.564 |
| MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.316 |
| TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.302 |
| TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.267 |
| TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.297 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HVB3 | Leptomonas seymouri | 66% | 100% |
| A0A0N1HZ27 | Leptomonas seymouri | 43% | 99% |
| A0A0S4JK63 | Bodo saltans | 30% | 100% |
| A0A0S4JP06 | Bodo saltans | 33% | 83% |
| A0A1X0NHK1 | Trypanosomatidae | 49% | 100% |
| A0A3Q8IJU9 | Leishmania donovani | 90% | 100% |
| A0A3R7RTY4 | Trypanosoma rangeli | 47% | 100% |
| A0A3S7X189 | Leishmania donovani | 41% | 99% |
| A2WSD3 | Oryza sativa subsp. indica | 24% | 94% |
| A2WSD8 | Oryza sativa subsp. indica | 25% | 92% |
| A2X3S3 | Oryza sativa subsp. indica | 28% | 92% |
| A2X5B4 | Oryza sativa subsp. indica | 26% | 75% |
| A2YZ24 | Oryza sativa subsp. indica | 27% | 90% |
| A3BWJ9 | Oryza sativa subsp. japonica | 28% | 93% |
| A4HG76 | Leishmania braziliensis | 42% | 99% |
| A4HQ04 | Leishmania braziliensis | 70% | 100% |
| A4I3B9 | Leishmania infantum | 41% | 99% |
| A4IDR5 | Leishmania infantum | 90% | 100% |
| B9G2E6 | Oryza sativa subsp. japonica | 26% | 87% |
| D3ZH22 | Rattus norvegicus | 26% | 100% |
| E9ATS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
| E9AZJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 99% |
| P0DKJ5 | Vitis vinifera | 26% | 83% |
| Q0J349 | Oryza sativa subsp. japonica | 27% | 90% |
| Q10LN5 | Oryza sativa subsp. japonica | 23% | 73% |
| Q19VE6 | Oryza sativa subsp. indica | 25% | 78% |
| Q290X1 | Drosophila pseudoobscura pseudoobscura | 27% | 100% |
| Q4Q8N5 | Leishmania major | 41% | 99% |
| Q54JW5 | Dictyostelium discoideum | 24% | 100% |
| Q5EAL3 | Xenopus tropicalis | 26% | 100% |
| Q5EB14 | Danio rerio | 28% | 100% |
| Q5NAZ9 | Oryza sativa subsp. japonica | 25% | 95% |
| Q6K4V2 | Oryza sativa subsp. japonica | 28% | 92% |
| Q6K602 | Oryza sativa subsp. japonica | 26% | 75% |
| Q6NQN5 | Arabidopsis thaliana | 25% | 91% |
| Q6NTJ7 | Xenopus laevis | 24% | 100% |
| Q6YZF3 | Oryza sativa subsp. japonica | 25% | 78% |
| Q7JVE7 | Drosophila melanogaster | 25% | 100% |
| Q84WN3 | Arabidopsis thaliana | 23% | 99% |
| Q8LBF7 | Arabidopsis thaliana | 28% | 93% |
| Q8LR09 | Oryza sativa subsp. japonica | 25% | 92% |
| Q8W0K2 | Oryza sativa subsp. japonica | 23% | 94% |
| Q944M5 | Arabidopsis thaliana | 24% | 95% |
| Q9C9M9 | Arabidopsis thaliana | 23% | 92% |
| Q9CXK4 | Mus musculus | 25% | 100% |
| Q9FGQ2 | Arabidopsis thaliana | 24% | 81% |
| Q9FM10 | Arabidopsis thaliana | 24% | 100% |
| Q9FY94 | Arabidopsis thaliana | 23% | 82% |
| Q9LUE3 | Arabidopsis thaliana | 28% | 83% |
| Q9SMM5 | Arabidopsis thaliana | 27% | 83% |
| Q9SW25 | Arabidopsis thaliana | 22% | 85% |
| Q9ZV02 | Arabidopsis thaliana | 26% | 93% |