Homologous to animal UDP-N-acetylglucosamine, UDP-galactose and CMP-sialic acid transporters. Only expanded in the Leptomonas lineage. 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: 2, no: 14 |
| NetGPI | no | yes: 0, no: 16 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000139 | Golgi membrane | 5 | 17 |
| GO:0016020 | membrane | 2 | 17 |
| GO:0031090 | organelle membrane | 3 | 17 |
| GO:0098588 | bounding membrane of organelle | 4 | 17 |
| GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: E9AWM5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 1 |
| GO:0006811 | monoatomic ion transport | 4 | 1 |
| GO:0006820 | monoatomic anion transport | 5 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0015711 | organic anion transport | 5 | 1 |
| GO:0015780 | nucleotide-sugar transmembrane transport | 3 | 1 |
| GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| GO:0055085 | transmembrane transport | 2 | 1 |
| GO:0071702 | organic substance transport | 4 | 1 |
| GO:0071705 | nitrogen compound transport | 4 | 1 |
| GO:0072334 | UDP-galactose transmembrane transport | 5 | 1 |
| GO:0090481 | pyrimidine nucleotide-sugar transmembrane transport | 4 | 1 |
| GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
| GO:1901264 | carbohydrate derivative transport | 5 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 17 |
| GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 17 |
| GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 17 |
| GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 17 |
| GO:0022857 | transmembrane transporter activity | 2 | 17 |
| GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 17 |
| GO:0005459 | UDP-galactose transmembrane transporter activity | 6 | 1 |
| GO:0015136 | sialic acid transmembrane transporter activity | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.481 |
| CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.336 |
| CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.468 |
| CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.318 |
| CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.354 |
| CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.354 |
| CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.357 |
| CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.463 |
| CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.452 |
| CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.411 |
| CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.386 |
| CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.338 |
| CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.703 |
| DOC_CKS1_1 | 444 | 449 | PF01111 | 0.311 |
| DOC_MAPK_gen_1 | 11 | 17 | PF00069 | 0.604 |
| DOC_MAPK_gen_1 | 156 | 166 | PF00069 | 0.557 |
| DOC_MAPK_gen_1 | 185 | 193 | PF00069 | 0.545 |
| DOC_MAPK_gen_1 | 195 | 202 | PF00069 | 0.500 |
| DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.338 |
| DOC_MAPK_MEF2A_6 | 157 | 166 | PF00069 | 0.522 |
| DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.353 |
| DOC_MAPK_MEF2A_6 | 265 | 274 | PF00069 | 0.288 |
| DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.579 |
| DOC_PP1_RVXF_1 | 243 | 249 | PF00149 | 0.440 |
| DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.633 |
| DOC_PP4_FxxP_1 | 444 | 447 | PF00568 | 0.334 |
| DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.774 |
| DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.714 |
| DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.342 |
| DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.330 |
| DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.553 |
| DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.759 |
| DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.562 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.633 |
| DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.380 |
| DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.711 |
| LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.548 |
| LIG_AP2alpha_1 | 391 | 395 | PF02296 | 0.354 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
| LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.440 |
| LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.354 |
| LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.438 |
| LIG_EH1_1 | 218 | 226 | PF00400 | 0.440 |
| LIG_EH1_1 | 451 | 459 | PF00400 | 0.310 |
| LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.554 |
| LIG_eIF4E_1 | 219 | 225 | PF01652 | 0.440 |
| LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.428 |
| LIG_FHA_1 | 157 | 163 | PF00498 | 0.736 |
| LIG_FHA_1 | 174 | 180 | PF00498 | 0.530 |
| LIG_FHA_1 | 394 | 400 | PF00498 | 0.328 |
| LIG_FHA_1 | 436 | 442 | PF00498 | 0.379 |
| LIG_FHA_1 | 67 | 73 | PF00498 | 0.341 |
| LIG_FHA_2 | 388 | 394 | PF00498 | 0.348 |
| LIG_GBD_Chelix_1 | 217 | 225 | PF00786 | 0.380 |
| LIG_HCF-1_HBM_1 | 203 | 206 | PF13415 | 0.562 |
| LIG_IRF3_LxIS_1 | 72 | 78 | PF10401 | 0.211 |
| LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.565 |
| LIG_LIR_Gen_1 | 236 | 246 | PF02991 | 0.309 |
| LIG_LIR_Gen_1 | 334 | 342 | PF02991 | 0.452 |
| LIG_LIR_Gen_1 | 428 | 439 | PF02991 | 0.393 |
| LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.428 |
| LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.298 |
| LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.439 |
| LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.344 |
| LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.284 |
| LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.404 |
| LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.349 |
| LIG_MLH1_MIPbox_1 | 388 | 392 | PF16413 | 0.354 |
| LIG_Pex14_1 | 9 | 13 | PF04695 | 0.679 |
| LIG_Pex14_2 | 188 | 192 | PF04695 | 0.501 |
| LIG_Pex14_2 | 329 | 333 | PF04695 | 0.428 |
| LIG_Pex14_2 | 366 | 370 | PF04695 | 0.440 |
| LIG_Pex14_2 | 387 | 391 | PF04695 | 0.309 |
| LIG_Pex14_2 | 427 | 431 | PF04695 | 0.428 |
| LIG_PTB_Apo_2 | 26 | 33 | PF02174 | 0.435 |
| LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.360 |
| LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.333 |
| LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.359 |
| LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.652 |
| LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.641 |
| LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.376 |
| LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.304 |
| LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.554 |
| LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.223 |
| LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.419 |
| LIG_Sin3_3 | 19 | 26 | PF02671 | 0.416 |
| LIG_SUMO_SIM_anti_2 | 208 | 215 | PF11976 | 0.528 |
| LIG_SUMO_SIM_anti_2 | 456 | 462 | PF11976 | 0.310 |
| LIG_SUMO_SIM_par_1 | 223 | 229 | PF11976 | 0.380 |
| LIG_SUMO_SIM_par_1 | 456 | 462 | PF11976 | 0.186 |
| LIG_TRFH_1 | 259 | 263 | PF08558 | 0.562 |
| LIG_TYR_ITIM | 363 | 368 | PF00017 | 0.452 |
| LIG_UBA3_1 | 224 | 231 | PF00899 | 0.380 |
| LIG_UBA3_1 | 87 | 92 | PF00899 | 0.642 |
| LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.489 |
| MOD_CDC14_SPxK_1 | 262 | 265 | PF00782 | 0.562 |
| MOD_CDK_SPxK_1 | 259 | 265 | PF00069 | 0.562 |
| MOD_CK1_1 | 104 | 110 | PF00069 | 0.777 |
| MOD_CK1_1 | 114 | 120 | PF00069 | 0.706 |
| MOD_CK1_1 | 127 | 133 | PF00069 | 0.728 |
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.593 |
| MOD_CK1_1 | 314 | 320 | PF00069 | 0.339 |
| MOD_CK1_1 | 331 | 337 | PF00069 | 0.195 |
| MOD_CK1_1 | 426 | 432 | PF00069 | 0.409 |
| MOD_CK2_1 | 127 | 133 | PF00069 | 0.608 |
| MOD_CK2_1 | 144 | 150 | PF00069 | 0.573 |
| MOD_CK2_1 | 298 | 304 | PF00069 | 0.370 |
| MOD_CK2_1 | 43 | 49 | PF00069 | 0.249 |
| MOD_CK2_1 | 464 | 470 | PF00069 | 0.211 |
| MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.415 |
| MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.516 |
| MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.357 |
| MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.324 |
| MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.296 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.722 |
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.716 |
| MOD_GSK3_1 | 124 | 131 | PF00069 | 0.641 |
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.714 |
| MOD_GSK3_1 | 144 | 151 | PF00069 | 0.715 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.644 |
| MOD_GSK3_1 | 306 | 313 | PF00069 | 0.338 |
| MOD_GSK3_1 | 314 | 321 | PF00069 | 0.292 |
| MOD_GSK3_1 | 349 | 356 | PF00069 | 0.496 |
| MOD_GSK3_1 | 433 | 440 | PF00069 | 0.324 |
| MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.457 |
| MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.562 |
| MOD_NEK2_1 | 152 | 157 | PF00069 | 0.611 |
| MOD_NEK2_1 | 226 | 231 | PF00069 | 0.381 |
| MOD_NEK2_1 | 274 | 279 | PF00069 | 0.409 |
| MOD_NEK2_1 | 318 | 323 | PF00069 | 0.315 |
| MOD_NEK2_1 | 349 | 354 | PF00069 | 0.492 |
| MOD_NEK2_1 | 387 | 392 | PF00069 | 0.353 |
| MOD_NEK2_1 | 435 | 440 | PF00069 | 0.344 |
| MOD_NEK2_1 | 448 | 453 | PF00069 | 0.275 |
| MOD_NEK2_1 | 458 | 463 | PF00069 | 0.344 |
| MOD_NEK2_1 | 61 | 66 | PF00069 | 0.345 |
| MOD_NEK2_1 | 75 | 80 | PF00069 | 0.251 |
| MOD_NEK2_2 | 437 | 442 | PF00069 | 0.435 |
| MOD_NEK2_2 | 80 | 85 | PF00069 | 0.236 |
| MOD_PIKK_1 | 135 | 141 | PF00454 | 0.593 |
| MOD_PIKK_1 | 344 | 350 | PF00454 | 0.373 |
| MOD_PKA_1 | 156 | 162 | PF00069 | 0.518 |
| MOD_PKA_1 | 344 | 350 | PF00069 | 0.373 |
| MOD_PKA_2 | 344 | 350 | PF00069 | 0.461 |
| MOD_PKA_2 | 353 | 359 | PF00069 | 0.468 |
| MOD_Plk_1 | 114 | 120 | PF00069 | 0.605 |
| MOD_Plk_1 | 124 | 130 | PF00069 | 0.688 |
| MOD_Plk_4 | 114 | 120 | PF00069 | 0.700 |
| MOD_Plk_4 | 206 | 212 | PF00069 | 0.561 |
| MOD_Plk_4 | 233 | 239 | PF00069 | 0.277 |
| MOD_Plk_4 | 387 | 393 | PF00069 | 0.295 |
| MOD_Plk_4 | 437 | 443 | PF00069 | 0.345 |
| MOD_Plk_4 | 448 | 454 | PF00069 | 0.265 |
| MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.759 |
| MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.562 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.631 |
| MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.380 |
| MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.718 |
| TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.310 |
| TRG_DiLeu_BaEn_2 | 114 | 120 | PF01217 | 0.585 |
| TRG_DiLeu_LyEn_5 | 95 | 100 | PF01217 | 0.533 |
| TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.365 |
| TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.664 |
| TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.535 |
| TRG_NES_CRM1_1 | 222 | 234 | PF08389 | 0.368 |
| TRG_NES_CRM1_1 | 406 | 421 | PF08389 | 0.330 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7L9 | Leptomonas seymouri | 51% | 100% |
| A0A0N1HVQ8 | Leptomonas seymouri | 24% | 87% |
| A0A0S4JHP4 | Bodo saltans | 26% | 98% |
| A0A1X0NTD6 | Trypanosomatidae | 31% | 100% |
| A0A3Q8IES0 | Leishmania donovani | 73% | 87% |
| A0A3S7WVZ3 | Leishmania donovani | 90% | 100% |
| A0A3S7WY47 | Leishmania donovani | 84% | 84% |
| A0A422P321 | Trypanosoma rangeli | 28% | 100% |
| A4HD92 | Leishmania braziliensis | 59% | 93% |
| A4HDA0 | Leishmania braziliensis | 58% | 93% |
| A4I0N2 | Leishmania infantum | 85% | 84% |
| D0AAP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
| E9AH47 | Leishmania infantum | 73% | 87% |
| E9AWM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
| Q4QAU5 | Leishmania major | 70% | 100% |
| Q6DCG9 | Xenopus laevis | 24% | 100% |
| Q8LGE9 | Arabidopsis thaliana | 24% | 100% |
| V5BLB8 | Trypanosoma cruzi | 29% | 100% |