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: A0A3S7WY47
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 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:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 2 |
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 |
GO:0008643 | carbohydrate 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 | 100 | 102 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.409 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.309 |
DEG_SPOP_SBC_1 | 521 | 525 | PF00917 | 0.175 |
DOC_CKS1_1 | 531 | 536 | PF01111 | 0.274 |
DOC_MAPK_gen_1 | 100 | 106 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 243 | 253 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 292 | 301 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.256 |
DOC_PP1_RVXF_1 | 265 | 271 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 330 | 336 | PF00149 | 0.397 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.246 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.572 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.331 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.579 |
DOC_USP7_MATH_2 | 202 | 208 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.778 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 441 | 448 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 5 | 12 | PF00244 | 0.620 |
LIG_AP2alpha_1 | 478 | 482 | PF02296 | 0.360 |
LIG_BIR_III_4 | 26 | 30 | PF00653 | 0.599 |
LIG_BRCT_BRCA1_1 | 420 | 424 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 475 | 479 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.432 |
LIG_CaM_IQ_9 | 236 | 251 | PF13499 | 0.567 |
LIG_CaMK_CASK_1 | 95 | 101 | PF00069 | 0.550 |
LIG_EH1_1 | 305 | 313 | PF00400 | 0.442 |
LIG_eIF4E_1 | 293 | 299 | PF01652 | 0.560 |
LIG_eIF4E_1 | 306 | 312 | PF01652 | 0.442 |
LIG_eIF4E_1 | 329 | 335 | PF01652 | 0.424 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.362 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.331 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.368 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.264 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.288 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.330 |
LIG_GBD_Chelix_1 | 304 | 312 | PF00786 | 0.321 |
LIG_HCF-1_HBM_1 | 290 | 293 | PF13415 | 0.515 |
LIG_IRF3_LxIS_1 | 161 | 167 | PF10401 | 0.214 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 421 | 429 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 480 | 490 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 515 | 526 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 543 | 552 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.770 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.353 |
LIG_MLH1_MIPbox_1 | 475 | 479 | PF16413 | 0.360 |
LIG_Pex14_1 | 98 | 102 | PF04695 | 0.727 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.518 |
LIG_Pex14_2 | 416 | 420 | PF04695 | 0.424 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.399 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.307 |
LIG_Pex14_2 | 514 | 518 | PF04695 | 0.411 |
LIG_PTB_Apo_2 | 115 | 122 | PF02174 | 0.442 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.375 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.522 |
LIG_SH3_2 | 32 | 37 | PF14604 | 0.597 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.594 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.584 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.592 |
LIG_Sin3_3 | 108 | 115 | PF02671 | 0.379 |
LIG_SUMO_SIM_anti_2 | 295 | 302 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.321 |
LIG_TRAF2_1 | 210 | 213 | PF00917 | 0.580 |
LIG_TRFH_1 | 346 | 350 | PF08558 | 0.515 |
LIG_TYR_ITIM | 450 | 455 | PF00017 | 0.379 |
LIG_UBA3_1 | 176 | 181 | PF00899 | 0.649 |
LIG_UBA3_1 | 311 | 318 | PF00899 | 0.321 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.486 |
LIG_WRC_WIRS_1 | 541 | 546 | PF05994 | 0.337 |
MOD_CDC14_SPxK_1 | 349 | 352 | PF00782 | 0.515 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.542 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.755 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.717 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.616 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.341 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.278 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.610 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.403 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.386 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.553 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.758 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.624 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.603 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.381 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.214 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.393 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.330 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.363 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.672 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.717 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.687 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.643 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.327 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.317 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.502 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.634 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.295 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.732 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.623 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.515 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.605 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.360 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.266 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.697 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.365 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.404 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.341 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.307 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.489 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.345 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.612 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.331 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.269 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.305 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.325 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.619 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.586 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.558 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.439 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.725 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.694 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.568 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.790 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.734 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.561 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.281 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.292 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.333 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.261 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.640 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.568 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.630 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.588 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.321 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.622 |
TRG_DiLeu_BaEn_2 | 203 | 209 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.700 |
TRG_NES_CRM1_1 | 309 | 321 | PF08389 | 0.321 |
TRG_NES_CRM1_1 | 493 | 508 | PF08389 | 0.314 |
TRG_NLS_Bipartite_1 | 18 | 40 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 35 | 40 | PF00514 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6R3 | Leptomonas seymouri | 23% | 100% |
A0A0N0P7L9 | Leptomonas seymouri | 52% | 100% |
A0A0S4JHP4 | Bodo saltans | 27% | 100% |
A0A1X0NTD6 | Trypanosomatidae | 30% | 100% |
A0A3Q8IES0 | Leishmania donovani | 79% | 95% |
A0A422P321 | Trypanosoma rangeli | 28% | 100% |
A4HD92 | Leishmania braziliensis | 60% | 94% |
A4HDA0 | Leishmania braziliensis | 60% | 94% |
A4I0N2 | Leishmania infantum | 99% | 100% |
D0AAP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AH47 | Leishmania infantum | 79% | 95% |
E9AWM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AWM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 94% |
Q4QAU5 | Leishmania major | 75% | 100% |
V5BLB8 | Trypanosoma cruzi | 28% | 100% |