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: 1, no: 6 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 8 |
GO:0016020 | membrane | 2 | 8 |
GO:0031090 | organelle membrane | 3 | 8 |
GO:0098588 | bounding membrane of organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9ARH7
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 | 8 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 8 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 8 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 8 |
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 | 0.325 |
CLV_C14_Caspase3-7 | 530 | 534 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.320 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.284 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.526 |
DOC_CYCLIN_RxL_1 | 241 | 252 | PF00134 | 0.566 |
DOC_CYCLIN_RxL_1 | 296 | 303 | PF00134 | 0.227 |
DOC_CYCLIN_yClb1_LxF_4 | 276 | 282 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 241 | 248 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 260 | 268 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 260 | 268 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 406 | 414 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 88 | 96 | PF00069 | 0.694 |
DOC_MAPK_NFAT4_5 | 261 | 269 | PF00069 | 0.525 |
DOC_MAPK_NFAT4_5 | 55 | 63 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 242 | 249 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 297 | 303 | PF00149 | 0.227 |
DOC_PP1_RVXF_1 | 447 | 453 | PF00149 | 0.361 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.388 |
DOC_PP4_FxxP_1 | 422 | 425 | PF00568 | 0.387 |
DOC_PP4_FxxP_1 | 455 | 458 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.320 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 179 | 183 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 339 | 346 | PF00244 | 0.274 |
LIG_Actin_WH2_2 | 180 | 195 | PF00022 | 0.701 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.742 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.387 |
LIG_BRCT_BRCA1_1 | 551 | 555 | PF00533 | 0.387 |
LIG_BRCT_BRCA1_2 | 397 | 403 | PF00533 | 0.388 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.525 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.633 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.712 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.549 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.360 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.362 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.325 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.509 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.484 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.314 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.387 |
LIG_LIR_Apic_2 | 420 | 425 | PF02991 | 0.387 |
LIG_LIR_Apic_2 | 453 | 458 | PF02991 | 0.195 |
LIG_LIR_Gen_1 | 393 | 404 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 488 | 497 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 552 | 560 | PF02991 | 0.480 |
LIG_LIR_LC3C_4 | 23 | 27 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.195 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.621 |
LIG_MLH1_MIPbox_1 | 397 | 401 | PF16413 | 0.388 |
LIG_MYND_3 | 89 | 93 | PF01753 | 0.561 |
LIG_NRP_CendR_1 | 561 | 562 | PF00754 | 0.475 |
LIG_Pex14_1 | 489 | 493 | PF04695 | 0.388 |
LIG_Pex14_2 | 267 | 271 | PF04695 | 0.454 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.204 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.304 |
LIG_REV1ctd_RIR_1 | 235 | 246 | PF16727 | 0.569 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.601 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.387 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.412 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.314 |
LIG_SH2_NCK_1 | 396 | 400 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.386 |
LIG_SH2_SRC | 535 | 538 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.782 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.258 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.754 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.726 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.707 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.319 |
LIG_SUMO_SIM_anti_2 | 11 | 17 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 23 | 29 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 518 | 525 | PF11976 | 0.305 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.700 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 430 | 435 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 545 | 552 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 95 | 103 | PF11976 | 0.701 |
LIG_UBA3_1 | 500 | 507 | PF00899 | 0.364 |
LIG_WW_3 | 187 | 191 | PF00397 | 0.590 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.755 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.729 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.773 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.701 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.594 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.310 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.195 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.326 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.533 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.567 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.556 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.423 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.356 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.507 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.349 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.800 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.795 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.618 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.376 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.228 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.311 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.540 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.195 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.195 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.470 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.454 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.749 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.688 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.577 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.552 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.347 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.373 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.349 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.242 |
MOD_NEK2_2 | 410 | 415 | PF00069 | 0.525 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.760 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.387 |
MOD_PK_1 | 100 | 106 | PF00069 | 0.626 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.525 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.619 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.753 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.525 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.510 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.295 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.643 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.344 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.624 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.364 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.327 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.507 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.283 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.214 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.367 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.318 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.757 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.633 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.687 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.515 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.638 |
TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.609 |
TRG_DiLeu_BaEn_1 | 93 | 98 | PF01217 | 0.700 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.466 |
TRG_NES_CRM1_1 | 51 | 66 | PF08389 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVQ8 | Leptomonas seymouri | 52% | 100% |
A0A3S7WUS3 | Leishmania donovani | 83% | 100% |
A0A422P321 | Trypanosoma rangeli | 27% | 100% |
A4H9E4 | Leishmania braziliensis | 61% | 100% |
A4HXR5 | Leishmania infantum | 83% | 100% |
Q5QHQ6 | Leishmania major | 81% | 100% |