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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 7 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0098588 | bounding membrane of organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q5QHQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006820 | monoatomic anion transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015711 | organic anion transport | 5 | 2 |
GO:0015780 | nucleotide-sugar transmembrane transport | 3 | 2 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072334 | UDP-galactose transmembrane transport | 5 | 2 |
GO:0090481 | pyrimidine nucleotide-sugar transmembrane transport | 4 | 2 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:1901264 | carbohydrate derivative transport | 5 | 2 |
GO:0008643 | carbohydrate transport | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 7 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 7 |
GO:0005459 | UDP-galactose transmembrane transporter activity | 6 | 2 |
GO:0015136 | sialic acid transmembrane transporter activity | 4 | 2 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 7 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 7 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.346 |
CLV_MEL_PAP_1 | 27 | 33 | PF00089 | 0.308 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.563 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.539 |
DOC_CYCLIN_yClb1_LxF_4 | 275 | 281 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 265 | 271 | PF00134 | 0.389 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 405 | 413 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 533 | 540 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 88 | 96 | PF00069 | 0.699 |
DOC_MAPK_NFAT4_5 | 260 | 268 | PF00069 | 0.546 |
DOC_MAPK_NFAT4_5 | 533 | 541 | PF00069 | 0.252 |
DOC_MAPK_NFAT4_5 | 55 | 63 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 446 | 452 | PF00149 | 0.405 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.436 |
DOC_PP4_FxxP_1 | 421 | 424 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 454 | 457 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 338 | 344 | PF00244 | 0.280 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.517 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.783 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 550 | 554 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_2 | 396 | 402 | PF00533 | 0.436 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.546 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.767 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.546 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.369 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.411 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.325 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.334 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.530 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.546 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.411 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.686 |
LIG_LIR_Apic_2 | 419 | 424 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 487 | 496 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 551 | 559 | PF02991 | 0.493 |
LIG_LIR_LC3C_4 | 14 | 17 | PF02991 | 0.428 |
LIG_LIR_LC3C_4 | 23 | 27 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.642 |
LIG_MLH1_MIPbox_1 | 396 | 400 | PF16413 | 0.436 |
LIG_NRBOX | 495 | 501 | PF00104 | 0.358 |
LIG_NRP_CendR_1 | 560 | 561 | PF00754 | 0.517 |
LIG_PCNA_PIPBox_1 | 242 | 251 | PF02747 | 0.536 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.389 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.513 |
LIG_Rb_pABgroove_1 | 182 | 190 | PF01858 | 0.648 |
LIG_REV1ctd_RIR_1 | 234 | 245 | PF16727 | 0.479 |
LIG_REV1ctd_RIR_1 | 475 | 485 | PF16727 | 0.336 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.411 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.363 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.310 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 507 | 511 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.338 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.741 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.782 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.650 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.748 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.330 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 23 | 29 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 517 | 524 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.696 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 95 | 103 | PF11976 | 0.705 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.765 |
LIG_UBA3_1 | 499 | 506 | PF00899 | 0.389 |
LIG_WRC_WIRS_1 | 554 | 559 | PF05994 | 0.518 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.753 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.680 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.536 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.452 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.308 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.373 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.393 |
MOD_Cter_Amidation | 310 | 313 | PF01082 | 0.363 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.583 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.619 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.363 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.486 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.371 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.411 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.411 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.770 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.721 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.773 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.520 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.431 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.392 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.546 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.503 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.501 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.756 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.525 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.411 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.299 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.319 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.411 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.411 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.546 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.411 |
MOD_PK_1 | 100 | 106 | PF00069 | 0.638 |
MOD_PKA_1 | 232 | 238 | PF00069 | 0.597 |
MOD_PKA_1 | 259 | 265 | PF00069 | 0.546 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.546 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.546 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.319 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.252 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.650 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.252 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.401 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.423 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.508 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.500 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.381 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.413 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.400 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.411 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.546 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.767 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.530 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.539 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.305 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.657 |
TRG_DiLeu_BaEn_1 | 93 | 98 | PF01217 | 0.696 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.582 |
TRG_NES_CRM1_1 | 51 | 66 | PF08389 | 0.619 |
TRG_NLS_MonoExtN_4 | 230 | 236 | PF00514 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVQ8 | Leptomonas seymouri | 52% | 100% |
A0A3S7WUS3 | Leishmania donovani | 85% | 100% |
A4H9E4 | Leishmania braziliensis | 62% | 100% |
A4HXR5 | Leishmania infantum | 86% | 100% |
E9ARH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |