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: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0098588 | bounding membrane of organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WUS3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0008643 | carbohydrate transport | 5 | 2 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
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 | 9 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 9 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 9 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 9 |
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 | 285 | 289 | PF00656 | 0.264 |
CLV_C14_Caspase3-7 | 531 | 535 | PF00656 | 0.261 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.251 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.192 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.240 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.240 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.473 |
DEG_SPOP_SBC_1 | 406 | 410 | PF00917 | 0.458 |
DOC_CYCLIN_RxL_1 | 241 | 248 | PF00134 | 0.537 |
DOC_CYCLIN_yClb1_LxF_4 | 276 | 282 | PF00134 | 0.295 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.276 |
DOC_MAPK_gen_1 | 260 | 268 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 260 | 268 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 407 | 415 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 88 | 96 | PF00069 | 0.601 |
DOC_MAPK_NFAT4_5 | 261 | 269 | PF00069 | 0.464 |
DOC_MAPK_NFAT4_5 | 55 | 63 | PF00069 | 0.451 |
DOC_PP1_RVXF_1 | 448 | 454 | PF00149 | 0.292 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.295 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.307 |
DOC_PP4_FxxP_1 | 423 | 426 | PF00568 | 0.295 |
DOC_PP4_FxxP_1 | 456 | 459 | PF00568 | 0.264 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.617 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.458 |
LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.642 |
LIG_Actin_WH2_2 | 180 | 195 | PF00022 | 0.627 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.425 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.687 |
LIG_BRCT_BRCA1_1 | 398 | 402 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 552 | 556 | PF00533 | 0.228 |
LIG_BRCT_BRCA1_2 | 398 | 404 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_2 | 552 | 558 | PF00533 | 0.260 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.464 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.717 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.700 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.489 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.284 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.315 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.295 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.264 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.285 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.451 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.473 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.288 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.314 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.574 |
LIG_GBD_Chelix_1 | 540 | 548 | PF00786 | 0.244 |
LIG_LIR_Apic_2 | 421 | 426 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 394 | 405 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 553 | 561 | PF02991 | 0.376 |
LIG_LIR_LC3C_4 | 23 | 27 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.586 |
LIG_MLH1_MIPbox_1 | 398 | 402 | PF16413 | 0.307 |
LIG_NRP_CendR_1 | 562 | 563 | PF00754 | 0.424 |
LIG_PCNA_PIPBox_1 | 243 | 252 | PF02747 | 0.544 |
LIG_Pex14_1 | 490 | 494 | PF04695 | 0.307 |
LIG_Pex14_2 | 267 | 271 | PF04695 | 0.343 |
LIG_Pex14_2 | 494 | 498 | PF04695 | 0.261 |
LIG_REV1ctd_RIR_1 | 477 | 487 | PF16727 | 0.259 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.592 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.295 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.299 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.253 |
LIG_SH2_SRC | 536 | 539 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.307 |
LIG_SH2_STAP1 | 484 | 488 | PF00017 | 0.251 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.464 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.683 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.688 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.646 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.251 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 23 | 29 | PF11976 | 0.329 |
LIG_SUMO_SIM_anti_2 | 519 | 526 | PF11976 | 0.276 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.683 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 322 | 327 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 431 | 436 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 546 | 553 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 95 | 103 | PF11976 | 0.628 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.680 |
LIG_UBA3_1 | 501 | 508 | PF00899 | 0.276 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.681 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.624 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.289 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.273 |
MOD_GlcNHglycan | 101 | 105 | PF01048 | 0.418 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.473 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.531 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.491 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.503 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.332 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.371 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.465 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.295 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.295 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.673 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.688 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.748 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.352 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.313 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.464 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.276 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.645 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.652 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.645 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.646 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.484 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.328 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.242 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.295 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.260 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.313 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.523 |
MOD_NEK2_2 | 411 | 416 | PF00069 | 0.472 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.295 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.226 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.464 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.679 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.464 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.464 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.583 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.670 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.327 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.329 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.475 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.373 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.307 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.339 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.346 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.467 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.687 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.673 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.470 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.458 |
TRG_DiLeu_BaEn_1 | 93 | 98 | PF01217 | 0.619 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.440 |
TRG_NES_CRM1_1 | 51 | 66 | PF08389 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVQ8 | Leptomonas seymouri | 54% | 100% |
A4H9E4 | Leishmania braziliensis | 65% | 99% |
A4HD92 | Leishmania braziliensis | 28% | 100% |
A4HDA0 | Leishmania braziliensis | 28% | 100% |
A4HXR5 | Leishmania infantum | 99% | 100% |
E9ARH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q5QHQ6 | Leishmania major | 85% | 100% |