Related to plant and animal nucleoside-sugar transporters, often localized to the Golgi apparatus.. An expanded family in kinetoplastids, possibly to cover the need for expanded proteoglycan biosynthesis. Localization: Golgi (by homology)
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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 3 |
GO:0016020 | membrane | 2 | 21 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
Related structures:
AlphaFold database: Q4Q726
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 3 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 3 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 3 |
GO:0015297 | antiporter activity | 5 | 3 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.264 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.479 |
DEG_MDM2_SWIB_1 | 214 | 222 | PF02201 | 0.255 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.307 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.235 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 104 | 110 | PF00134 | 0.316 |
DOC_MAPK_gen_1 | 119 | 129 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 315 | 322 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 102 | 111 | PF00069 | 0.338 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 315 | 322 | PF00069 | 0.543 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.676 |
LIG_APCC_ABBA_1 | 108 | 113 | PF00400 | 0.193 |
LIG_APCC_ABBAyCdc20_2 | 25 | 31 | PF00400 | 0.255 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.254 |
LIG_deltaCOP1_diTrp_1 | 145 | 155 | PF00928 | 0.217 |
LIG_EH1_1 | 97 | 105 | PF00400 | 0.409 |
LIG_eIF4E_1 | 251 | 257 | PF01652 | 0.289 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.515 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.300 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.392 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.511 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.342 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.453 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.299 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.401 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.298 |
LIG_GBD_Chelix_1 | 248 | 256 | PF00786 | 0.365 |
LIG_IRF3_LxIS_1 | 69 | 76 | PF10401 | 0.438 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 261 | 270 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 288 | 297 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.171 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.449 |
LIG_NRBOX | 122 | 128 | PF00104 | 0.507 |
LIG_NRBOX | 6 | 12 | PF00104 | 0.409 |
LIG_PCNA_PIPBox_1 | 149 | 158 | PF02747 | 0.235 |
LIG_PDZ_Class_2 | 320 | 325 | PF00595 | 0.705 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.345 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.262 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.354 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.290 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.236 |
LIG_PTB_Apo_2 | 158 | 165 | PF02174 | 0.289 |
LIG_PTB_Apo_2 | 21 | 28 | PF02174 | 0.394 |
LIG_PTB_Phospho_1 | 158 | 164 | PF10480 | 0.289 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.289 |
LIG_SH3_1 | 291 | 297 | PF00018 | 0.613 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.366 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 124 | 131 | PF11976 | 0.277 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 278 | 283 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 37 | 44 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.379 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.202 |
LIG_WW_2 | 294 | 297 | PF00397 | 0.509 |
MOD_CDK_SPK_2 | 60 | 65 | PF00069 | 0.527 |
MOD_CDK_SPxK_1 | 60 | 66 | PF00069 | 0.417 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.309 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.448 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.658 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.683 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.309 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.434 |
MOD_Cter_Amidation | 117 | 120 | PF01082 | 0.327 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.260 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.525 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.486 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.448 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.311 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.448 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.622 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.255 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.306 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.409 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.313 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.307 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.356 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.333 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.254 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.307 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.339 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.238 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.332 |
MOD_PK_1 | 65 | 71 | PF00069 | 0.457 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.473 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.750 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.254 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.289 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.217 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.299 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.456 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.297 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.318 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.432 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.267 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.280 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.258 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.297 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.320 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.255 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.299 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.394 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.448 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.693 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.192 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.551 |
TRG_PTS2 | 1 | 34 | PF00400 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N6 | Leptomonas seymouri | 39% | 100% |
A0A0N1PAW1 | Leptomonas seymouri | 74% | 100% |
A0A0S4IKX4 | Bodo saltans | 36% | 100% |
A0A0S4JRZ1 | Bodo saltans | 37% | 100% |
A0A1X0P276 | Trypanosomatidae | 67% | 100% |
A0A1X0P5Z4 | Trypanosomatidae | 43% | 100% |
A0A3R7NGZ9 | Trypanosoma rangeli | 64% | 100% |
A0A3S7WVL9 | Leishmania donovani | 37% | 100% |
A0A3S7X3R1 | Leishmania donovani | 93% | 100% |
A0A422NUS0 | Trypanosoma rangeli | 40% | 100% |
A4HAA0 | Leishmania braziliensis | 37% | 100% |
A4HYI0 | Leishmania infantum | 37% | 100% |
A4I5U5 | Leishmania infantum | 93% | 100% |
A4IFK2 | Bos taurus | 34% | 100% |
C9ZR66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9ASA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B140 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4IHS9 | Arabidopsis thaliana | 31% | 95% |
P49131 | Flaveria pringlei | 25% | 80% |
P49132 | Flaveria trinervia | 25% | 80% |
P49133 | Zea mays | 26% | 79% |
Q1JQ66 | Danio rerio | 35% | 100% |
Q3E6T0 | Arabidopsis thaliana | 26% | 93% |
Q4QD58 | Leishmania major | 35% | 100% |
Q550W6 | Dictyostelium discoideum | 23% | 88% |
Q5XF09 | Arabidopsis thaliana | 28% | 100% |
Q6DBP3 | Arabidopsis thaliana | 27% | 100% |
Q6PGC7 | Mus musculus | 35% | 100% |
Q7Z769 | Homo sapiens | 35% | 100% |
Q8GUJ1 | Arabidopsis thaliana | 33% | 92% |
Q8RWW7 | Arabidopsis thaliana | 30% | 96% |
Q8RXL8 | Arabidopsis thaliana | 30% | 91% |
Q94EI9 | Arabidopsis thaliana | 26% | 96% |
Q9C521 | Arabidopsis thaliana | 26% | 97% |
Q9C8M1 | Arabidopsis thaliana | 28% | 98% |
Q9FDZ5 | Arabidopsis thaliana | 28% | 97% |
Q9FG70 | Arabidopsis thaliana | 27% | 82% |
Q9FIH5 | Arabidopsis thaliana | 29% | 93% |
Q9FTT3 | Oryza sativa subsp. japonica | 25% | 78% |
Q9FYE5 | Arabidopsis thaliana | 27% | 100% |
Q9LDH3 | Arabidopsis thaliana | 25% | 90% |
Q9LFN3 | Arabidopsis thaliana | 27% | 93% |
Q9LNH5 | Arabidopsis thaliana | 28% | 89% |
Q9LPU2 | Arabidopsis thaliana | 30% | 93% |
Q9LRP2 | Arabidopsis thaliana | 29% | 87% |
Q9LU76 | Arabidopsis thaliana | 27% | 83% |
Q9SFE9 | Arabidopsis thaliana | 28% | 95% |
Q9SKJ7 | Arabidopsis thaliana | 25% | 94% |
Q9SRE4 | Arabidopsis thaliana | 29% | 94% |
Q9SS40 | Arabidopsis thaliana | 27% | 92% |
Q9SUV2 | Arabidopsis thaliana | 27% | 93% |
Q9SZ96 | Arabidopsis thaliana | 29% | 97% |
V5BMW3 | Trypanosoma cruzi | 60% | 100% |
V5D4Q6 | Trypanosoma cruzi | 41% | 100% |