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: 16 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 19 |
GO:0016020 | membrane | 2 | 19 |
GO:0031090 | organelle membrane | 3 | 19 |
GO:0098588 | bounding membrane of organelle | 4 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: A4HDA0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0008643 | carbohydrate transport | 5 | 1 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
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:0055085 | transmembrane transport | 2 | 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 | 19 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 19 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 19 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 19 |
GO:0022857 | transmembrane transporter activity | 2 | 19 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 19 |
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_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.354 |
CLV_PCSK_FUR_1 | 9 | 13 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.264 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.627 |
DOC_MAPK_gen_1 | 166 | 174 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 176 | 183 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 186 | 194 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 246 | 255 | PF00069 | 0.238 |
DOC_MAPK_RevD_3 | 155 | 168 | PF00069 | 0.373 |
DOC_PP1_RVXF_1 | 224 | 230 | PF00149 | 0.411 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.351 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.534 |
LIG_AP2alpha_1 | 372 | 376 | PF02296 | 0.332 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 408 | 412 | PF00533 | 0.406 |
LIG_EH1_1 | 199 | 207 | PF00400 | 0.408 |
LIG_eIF4E_1 | 187 | 193 | PF01652 | 0.532 |
LIG_eIF4E_1 | 200 | 206 | PF01652 | 0.408 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.218 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.344 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.257 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.331 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.254 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.331 |
LIG_GBD_Chelix_1 | 344 | 352 | PF00786 | 0.315 |
LIG_GBD_Chelix_1 | 76 | 84 | PF00786 | 0.192 |
LIG_HCF-1_HBM_1 | 184 | 187 | PF13415 | 0.475 |
LIG_LIR_Gen_1 | 216 | 227 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 315 | 323 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 374 | 384 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 409 | 420 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 82 | 93 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.320 |
LIG_MLH1_MIPbox_1 | 369 | 373 | PF16413 | 0.332 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.532 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.408 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.277 |
LIG_Pex14_2 | 408 | 412 | PF04695 | 0.391 |
LIG_PTB_Apo_2 | 26 | 33 | PF02174 | 0.400 |
LIG_PTB_Phospho_1 | 26 | 32 | PF10480 | 0.379 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.279 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.532 |
LIG_Sin3_3 | 19 | 26 | PF02671 | 0.307 |
LIG_SUMO_SIM_anti_2 | 302 | 307 | PF11976 | 0.185 |
LIG_TRFH_1 | 240 | 244 | PF08558 | 0.475 |
LIG_TYR_ITIM | 344 | 349 | PF00017 | 0.328 |
LIG_UBA3_1 | 33 | 37 | PF00899 | 0.185 |
LIG_UBA3_1 | 445 | 450 | PF00899 | 0.185 |
LIG_WRC_WIRS_1 | 369 | 374 | PF05994 | 0.248 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.452 |
MOD_CDC14_SPxK_1 | 243 | 246 | PF00782 | 0.475 |
MOD_CDK_SPxK_1 | 240 | 246 | PF00069 | 0.475 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.231 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.348 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.219 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.373 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.249 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.502 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.368 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.348 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.291 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.344 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.272 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.285 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.173 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.288 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.475 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.251 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.341 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.455 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.327 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.333 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.279 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.332 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.293 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.400 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.255 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.254 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.191 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.239 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.276 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.293 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.295 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.242 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.235 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.321 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.596 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.758 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.667 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.534 |
TRG_DiLeu_BaEn_1 | 75 | 80 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.683 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7L9 | Leptomonas seymouri | 49% | 100% |
A0A0N1HVQ8 | Leptomonas seymouri | 23% | 84% |
A0A0S4JHP4 | Bodo saltans | 29% | 94% |
A0A1X0NTD6 | Trypanosomatidae | 30% | 100% |
A0A3Q8IES0 | Leishmania donovani | 71% | 84% |
A0A3S7WUS3 | Leishmania donovani | 28% | 80% |
A0A3S7WVZ3 | Leishmania donovani | 71% | 100% |
A0A3S7WY47 | Leishmania donovani | 60% | 81% |
A0A422P321 | Trypanosoma rangeli | 31% | 100% |
A4HD92 | Leishmania braziliensis | 99% | 100% |
A4HXR5 | Leishmania infantum | 28% | 80% |
A4I0N2 | Leishmania infantum | 60% | 81% |
B8A7Q8 | Oryza sativa subsp. indica | 24% | 100% |
D0AAP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AH47 | Leishmania infantum | 71% | 84% |
E9AWM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 96% |
E9AWM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4QAU5 | Leishmania major | 70% | 100% |
Q5N855 | Oryza sativa subsp. japonica | 24% | 100% |
V5BLB8 | Trypanosoma cruzi | 30% | 100% |