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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A4HQ04
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 16 |
GO:0008643 | carbohydrate transport | 5 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0071702 | organic substance transport | 4 | 16 |
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_NRD_NRD_1 | 221 | 223 | PF00675 | 0.262 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.244 |
DEG_SPOP_SBC_1 | 97 | 101 | PF00917 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 152 | 158 | PF00134 | 0.305 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 193 | 200 | PF00069 | 0.251 |
DOC_PP2B_PxIxI_1 | 22 | 28 | PF00149 | 0.370 |
DOC_PP2B_PxIxI_1 | 5 | 11 | PF00149 | 0.332 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.434 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.264 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 104 | 108 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.434 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.165 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.234 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.260 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.373 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.156 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.354 |
LIG_LIR_Gen_1 | 109 | 120 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.216 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.205 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.262 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.242 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.369 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.275 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.286 |
LIG_SH2_PTP2 | 197 | 200 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.286 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.484 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.240 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.199 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.315 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.290 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.311 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.614 |
MOD_Cter_Amidation | 219 | 222 | PF01082 | 0.238 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.315 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.336 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.268 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.275 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.412 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.614 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.539 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.156 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.321 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.357 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.250 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.322 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.305 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.623 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.281 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.264 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.441 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.537 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.156 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.290 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.297 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.259 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.301 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.264 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.302 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.697 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.264 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVB3 | Leptomonas seymouri | 66% | 100% |
A0A0N1HZ27 | Leptomonas seymouri | 43% | 99% |
A0A0S4JK63 | Bodo saltans | 29% | 100% |
A0A0S4JP06 | Bodo saltans | 37% | 83% |
A0A1X0NHK1 | Trypanosomatidae | 46% | 100% |
A0A3Q8IJU9 | Leishmania donovani | 73% | 100% |
A0A3R7RTY4 | Trypanosoma rangeli | 48% | 100% |
A0A3S7X189 | Leishmania donovani | 40% | 99% |
A2WR31 | Oryza sativa subsp. indica | 30% | 98% |
A2WSD3 | Oryza sativa subsp. indica | 25% | 94% |
A2WSD8 | Oryza sativa subsp. indica | 26% | 92% |
A2X3S3 | Oryza sativa subsp. indica | 28% | 92% |
A2X5B4 | Oryza sativa subsp. indica | 29% | 75% |
A2YZ24 | Oryza sativa subsp. indica | 30% | 90% |
A3BWJ9 | Oryza sativa subsp. japonica | 30% | 93% |
A4HG76 | Leishmania braziliensis | 41% | 100% |
A4I3B9 | Leishmania infantum | 40% | 99% |
A4IDR5 | Leishmania infantum | 72% | 100% |
B9G2E6 | Oryza sativa subsp. japonica | 30% | 87% |
E9ATS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AZJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 99% |
O82587 | Arabidopsis thaliana | 26% | 84% |
P0DKJ4 | Sorghum bicolor | 28% | 98% |
P0DKJ5 | Vitis vinifera | 26% | 83% |
Q0J349 | Oryza sativa subsp. japonica | 29% | 90% |
Q290X1 | Drosophila pseudoobscura pseudoobscura | 28% | 100% |
Q4Q0S5 | Leishmania major | 70% | 100% |
Q4Q8N5 | Leishmania major | 42% | 100% |
Q54JW5 | Dictyostelium discoideum | 24% | 100% |
Q5JJY5 | Oryza sativa subsp. japonica | 30% | 98% |
Q5NAZ9 | Oryza sativa subsp. japonica | 25% | 95% |
Q6K4V2 | Oryza sativa subsp. japonica | 28% | 92% |
Q6K602 | Oryza sativa subsp. japonica | 27% | 75% |
Q6L568 | Oryza sativa subsp. japonica | 24% | 100% |
Q6NQN5 | Arabidopsis thaliana | 23% | 91% |
Q8LBF7 | Arabidopsis thaliana | 29% | 93% |
Q8LR09 | Oryza sativa subsp. japonica | 26% | 92% |
Q8W0K2 | Oryza sativa subsp. japonica | 25% | 94% |
Q944M5 | Arabidopsis thaliana | 29% | 95% |
Q9C9M9 | Arabidopsis thaliana | 27% | 92% |
Q9FGQ2 | Arabidopsis thaliana | 23% | 81% |
Q9FM10 | Arabidopsis thaliana | 27% | 100% |
Q9FY94 | Arabidopsis thaliana | 24% | 82% |
Q9LUE3 | Arabidopsis thaliana | 27% | 83% |
Q9SMM5 | Arabidopsis thaliana | 28% | 83% |
Q9SW25 | Arabidopsis thaliana | 25% | 85% |