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: A4IDR5
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 | 2 |
GO:0015144 | carbohydrate transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0051119 | sugar transmembrane transporter activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.306 |
DOC_CYCLIN_yCln2_LP_2 | 152 | 158 | PF00134 | 0.318 |
DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.222 |
DOC_MAPK_gen_1 | 31 | 41 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.197 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.506 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.222 |
DOC_PP2B_PxIxI_1 | 22 | 28 | PF00149 | 0.382 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.316 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 83 | 101 | PF00022 | 0.422 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.388 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.382 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.231 |
LIG_EH1_1 | 114 | 122 | PF00400 | 0.313 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.260 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.635 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.335 |
LIG_GBD_Chelix_1 | 117 | 125 | PF00786 | 0.319 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.215 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 83 | 90 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.272 |
LIG_NRBOX | 115 | 121 | PF00104 | 0.251 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.380 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.308 |
LIG_Pex3_1 | 119 | 130 | PF04882 | 0.241 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.288 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.283 |
LIG_SH2_PTP2 | 197 | 200 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.283 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.492 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.250 |
LIG_SUMO_SIM_par_1 | 190 | 195 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 22 | 29 | PF11976 | 0.375 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.327 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.303 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.536 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.208 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.361 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.276 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.482 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.254 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.486 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.438 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.318 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.334 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.384 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.270 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.415 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.337 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.509 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.488 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.335 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.294 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.232 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.326 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.303 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.337 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.304 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.313 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.276 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.316 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.247 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVB3 | Leptomonas seymouri | 67% | 100% |
A0A0N1HZ27 | Leptomonas seymouri | 40% | 99% |
A0A0S4JK63 | Bodo saltans | 30% | 100% |
A0A0S4JP06 | Bodo saltans | 34% | 83% |
A0A1X0NHK1 | Trypanosomatidae | 50% | 100% |
A0A3Q8IJU9 | Leishmania donovani | 100% | 100% |
A0A3R7RTY4 | Trypanosoma rangeli | 49% | 100% |
A0A3S7X189 | Leishmania donovani | 42% | 99% |
A2WSD3 | Oryza sativa subsp. indica | 22% | 94% |
A2WSD8 | Oryza sativa subsp. indica | 22% | 92% |
A2X3S3 | Oryza sativa subsp. indica | 25% | 92% |
A2X5B4 | Oryza sativa subsp. indica | 23% | 75% |
A2YZ24 | Oryza sativa subsp. indica | 28% | 90% |
A3BWJ9 | Oryza sativa subsp. japonica | 26% | 93% |
A4HG76 | Leishmania braziliensis | 40% | 100% |
A4HQ04 | Leishmania braziliensis | 72% | 100% |
A4I3B9 | Leishmania infantum | 42% | 100% |
B9G2E6 | Oryza sativa subsp. japonica | 25% | 87% |
D3ZH22 | Rattus norvegicus | 25% | 100% |
E9ATS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AZJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
O82587 | Arabidopsis thaliana | 26% | 84% |
P0DKJ5 | Vitis vinifera | 24% | 83% |
Q0J349 | Oryza sativa subsp. japonica | 28% | 90% |
Q10LN5 | Oryza sativa subsp. japonica | 22% | 73% |
Q290X1 | Drosophila pseudoobscura pseudoobscura | 23% | 100% |
Q4Q0S5 | Leishmania major | 90% | 100% |
Q4Q8N5 | Leishmania major | 42% | 100% |
Q54JW5 | Dictyostelium discoideum | 24% | 100% |
Q5EAL3 | Xenopus tropicalis | 25% | 100% |
Q5EB14 | Danio rerio | 27% | 100% |
Q5NAZ9 | Oryza sativa subsp. japonica | 24% | 95% |
Q6K4V2 | Oryza sativa subsp. japonica | 25% | 92% |
Q6K602 | Oryza sativa subsp. japonica | 23% | 75% |
Q6NQN5 | Arabidopsis thaliana | 26% | 91% |
Q6NTJ7 | Xenopus laevis | 23% | 100% |
Q8LBF7 | Arabidopsis thaliana | 26% | 93% |
Q8LR09 | Oryza sativa subsp. japonica | 22% | 92% |
Q8W0K2 | Oryza sativa subsp. japonica | 22% | 94% |
Q9C9M9 | Arabidopsis thaliana | 24% | 92% |
Q9CXK4 | Mus musculus | 24% | 100% |
Q9FGQ2 | Arabidopsis thaliana | 22% | 81% |
Q9FM10 | Arabidopsis thaliana | 24% | 100% |
Q9FY94 | Arabidopsis thaliana | 23% | 82% |
Q9LUE3 | Arabidopsis thaliana | 28% | 83% |
Q9SW25 | Arabidopsis thaliana | 22% | 85% |