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: 7 |
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: A4H9E4
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 | 221 | 225 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.265 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.413 |
CLV_MEL_PAP_1 | 27 | 33 | PF00089 | 0.235 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.265 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.459 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.213 |
DOC_CYCLIN_RxL_1 | 188 | 198 | PF00134 | 0.578 |
DOC_CYCLIN_yClb1_LxF_4 | 274 | 280 | PF00134 | 0.297 |
DOC_MAPK_gen_1 | 258 | 266 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 258 | 266 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 403 | 411 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.465 |
DOC_MAPK_NFAT4_5 | 259 | 267 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 444 | 450 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.297 |
DOC_PP4_FxxP_1 | 419 | 422 | PF00568 | 0.297 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.265 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.253 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.231 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.246 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.444 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.224 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.213 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.350 |
LIG_BRCT_BRCA1_1 | 548 | 552 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_2 | 548 | 554 | PF00533 | 0.261 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.465 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.612 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.508 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.305 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.301 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.465 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.302 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.297 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.468 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.413 |
LIG_GBD_Chelix_1 | 517 | 525 | PF00786 | 0.224 |
LIG_GBD_Chelix_1 | 536 | 544 | PF00786 | 0.282 |
LIG_GBD_Chelix_1 | 57 | 65 | PF00786 | 0.213 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 485 | 494 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 549 | 557 | PF02991 | 0.385 |
LIG_LIR_LC3C_4 | 23 | 27 | PF02991 | 0.287 |
LIG_LIR_LC3C_4 | 320 | 323 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.377 |
LIG_MLH1_MIPbox_1 | 472 | 476 | PF16413 | 0.213 |
LIG_NRBOX | 493 | 499 | PF00104 | 0.255 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.350 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.563 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.488 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.297 |
LIG_SH2_NCK_1 | 438 | 442 | PF00017 | 0.303 |
LIG_SH2_SRC | 480 | 483 | PF00017 | 0.254 |
LIG_SH2_SRC | 532 | 535 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.213 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 475 | 478 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.240 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.216 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.296 |
LIG_SUMO_SIM_anti_2 | 23 | 29 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 320 | 325 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.288 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.523 |
LIG_UBA3_1 | 61 | 70 | PF00899 | 0.413 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.243 |
LIG_WRC_WIRS_1 | 471 | 476 | PF05994 | 0.213 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.298 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.611 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.236 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.509 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.488 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.493 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.537 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.483 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.349 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.340 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.433 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.413 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.297 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.413 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.440 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.315 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.305 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.185 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.774 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.786 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.680 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.549 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.563 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.318 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.213 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.297 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.490 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.288 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.474 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.421 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.620 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.658 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.729 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.538 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.316 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.413 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.268 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.337 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.275 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.318 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.535 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.465 |
MOD_NEK2_2 | 470 | 475 | PF00069 | 0.213 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.633 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.297 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.465 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.413 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.691 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.581 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.466 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.492 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.249 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.480 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.645 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.643 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.343 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.587 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.296 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.487 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.302 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.314 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.470 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.221 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.471 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.246 |
MOD_SUMO_rev_2 | 305 | 314 | PF00179 | 0.224 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.651 |
TRG_NES_CRM1_1 | 51 | 66 | PF08389 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVQ8 | Leptomonas seymouri | 49% | 100% |
A0A3S7WUS3 | Leishmania donovani | 65% | 99% |
A4HXR5 | Leishmania infantum | 65% | 99% |
E9AQ83 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9ARH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 99% |
Q5QHQ6 | Leishmania major | 62% | 100% |