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: 13 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 16 |
GO:0016020 | membrane | 2 | 16 |
GO:0031090 | organelle membrane | 3 | 16 |
GO:0098588 | bounding membrane of organelle | 4 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4QAU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
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 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 16 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 16 |
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 | 16 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.426 |
CLV_PCSK_FUR_1 | 75 | 79 | PF00082 | 0.455 |
CLV_PCSK_FUR_1 | 95 | 99 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 23 | 31 | PF00400 | 0.571 |
DEG_SCF_TRCP1_1 | 264 | 269 | PF00400 | 0.781 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.630 |
DOC_CKS1_1 | 574 | 579 | PF01111 | 0.330 |
DOC_CYCLIN_RxL_1 | 305 | 314 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 325 | 332 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 335 | 344 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 24 | 32 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.379 |
DOC_MAPK_NFAT4_5 | 25 | 33 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 373 | 379 | PF00149 | 0.427 |
DOC_PP1_RVXF_1 | 525 | 532 | PF00149 | 0.290 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.579 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.685 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.388 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.649 |
LIG_AP2alpha_1 | 521 | 525 | PF02296 | 0.376 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.596 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.581 |
LIG_BIR_III_4 | 85 | 89 | PF00653 | 0.636 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_1 | 557 | 561 | PF00533 | 0.462 |
LIG_EH1_1 | 348 | 356 | PF00400 | 0.462 |
LIG_eIF4E_1 | 336 | 342 | PF01652 | 0.576 |
LIG_eIF4E_1 | 349 | 355 | PF01652 | 0.462 |
LIG_eIF4E_1 | 372 | 378 | PF01652 | 0.449 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.592 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.639 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.375 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.746 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.335 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.402 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.278 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.350 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.376 |
LIG_GBD_Chelix_1 | 347 | 355 | PF00786 | 0.398 |
LIG_HCF-1_HBM_1 | 333 | 336 | PF13415 | 0.590 |
LIG_LIR_Apic_2 | 152 | 156 | PF02991 | 0.609 |
LIG_LIR_Apic_2 | 194 | 198 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 231 | 242 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 366 | 376 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 46 | 54 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 464 | 472 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 558 | 569 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 586 | 595 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.430 |
LIG_MLH1_MIPbox_1 | 518 | 522 | PF16413 | 0.376 |
LIG_Pex14_1 | 158 | 162 | PF04695 | 0.736 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.527 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.449 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.462 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.351 |
LIG_Pex14_2 | 557 | 561 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 175 | 182 | PF02174 | 0.462 |
LIG_PTB_Phospho_1 | 175 | 181 | PF10480 | 0.449 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.391 |
LIG_SH2_STAT3 | 187 | 190 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 349 | 352 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.472 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.592 |
LIG_SH3_2 | 91 | 96 | PF14604 | 0.626 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.602 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.665 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.666 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.229 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.627 |
LIG_SH3_CIN85_PxpxPR_1 | 35 | 40 | PF14604 | 0.592 |
LIG_Sin3_3 | 168 | 175 | PF02671 | 0.482 |
LIG_SUMO_SIM_par_1 | 181 | 186 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.398 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.493 |
LIG_TRFH_1 | 389 | 393 | PF08558 | 0.590 |
LIG_TYR_ITIM | 493 | 498 | PF00017 | 0.482 |
LIG_UBA3_1 | 354 | 361 | PF00899 | 0.398 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.581 |
LIG_WRC_WIRS_1 | 229 | 234 | PF05994 | 0.370 |
LIG_WRC_WIRS_1 | 554 | 559 | PF05994 | 0.528 |
LIG_WRC_WIRS_1 | 584 | 589 | PF05994 | 0.372 |
LIG_WW_3 | 37 | 41 | PF00397 | 0.594 |
MOD_CDC14_SPxK_1 | 392 | 395 | PF00782 | 0.590 |
MOD_CDK_SPK_2 | 273 | 278 | PF00069 | 0.613 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.610 |
MOD_CDK_SPxK_1 | 389 | 395 | PF00069 | 0.590 |
MOD_CDK_SPxxK_3 | 33 | 40 | PF00069 | 0.594 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.631 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.579 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.587 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.660 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.711 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.376 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.219 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.431 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.651 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.404 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.491 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.466 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.589 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.376 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.355 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.309 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.612 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.776 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.439 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.737 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.725 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.341 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.290 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.338 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.651 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.614 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.590 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.637 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.392 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.336 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.580 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.506 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.407 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.350 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.341 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.531 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.373 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.361 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.287 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.366 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.593 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.674 |
MOD_NEK2_2 | 567 | 572 | PF00069 | 0.458 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.347 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.772 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.631 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.673 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.621 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.594 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.394 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.312 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.338 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.359 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.300 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.595 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.687 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.750 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.773 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.592 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.576 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.451 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.611 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.612 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.596 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.616 |
TRG_NES_CRM1_1 | 352 | 364 | PF08389 | 0.398 |
TRG_NES_CRM1_1 | 536 | 551 | PF08389 | 0.374 |
TRG_NLS_Bipartite_1 | 77 | 99 | PF00514 | 0.637 |
TRG_NLS_MonoCore_2 | 94 | 99 | PF00514 | 0.590 |
TRG_NLS_MonoExtN_4 | 94 | 100 | PF00514 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7L9 | Leptomonas seymouri | 52% | 100% |
A0A0N1HVQ8 | Leptomonas seymouri | 28% | 100% |
A0A1X0NTD6 | Trypanosomatidae | 30% | 100% |
A0A3Q8IES0 | Leishmania donovani | 90% | 100% |
A0A3S7WY47 | Leishmania donovani | 75% | 100% |
A0A422P321 | Trypanosoma rangeli | 30% | 100% |
A4HD92 | Leishmania braziliensis | 70% | 100% |
A4HDA0 | Leishmania braziliensis | 70% | 100% |
A4I0N2 | Leishmania infantum | 75% | 100% |
D0AAP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AH47 | Leishmania infantum | 90% | 100% |
E9AWM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9AWM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BLB8 | Trypanosoma cruzi | 30% | 100% |