N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. 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: 35 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A4H8M6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.378 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.315 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.498 |
CLV_PCSK_FUR_1 | 223 | 227 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.436 |
DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.363 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.285 |
DOC_MAPK_gen_1 | 110 | 120 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 278 | 287 | PF00069 | 0.529 |
DOC_MAPK_HePTP_8 | 306 | 318 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 113 | 122 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 188 | 197 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 309 | 318 | PF00069 | 0.643 |
DOC_MAPK_MEF2A_6 | 375 | 382 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 515 | 522 | PF00149 | 0.450 |
DOC_PP1_SILK_1 | 59 | 64 | PF00149 | 0.317 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.339 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.470 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.562 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 22 | 31 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 379 | 383 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 80 | 88 | PF00244 | 0.518 |
LIG_BIR_III_2 | 231 | 235 | PF00653 | 0.515 |
LIG_BIR_III_4 | 436 | 440 | PF00653 | 0.392 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.625 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.573 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.515 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.367 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.506 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.491 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.464 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.546 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.499 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.583 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.436 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 533 | 537 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 312 | 322 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 82 | 93 | PF02991 | 0.351 |
LIG_LIR_LC3C_4 | 504 | 509 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.508 |
LIG_PTB_Apo_2 | 280 | 287 | PF02174 | 0.477 |
LIG_PTB_Apo_2 | 29 | 36 | PF02174 | 0.459 |
LIG_PTB_Phospho_1 | 280 | 286 | PF10480 | 0.527 |
LIG_PTB_Phospho_1 | 29 | 35 | PF10480 | 0.463 |
LIG_RPA_C_Fungi | 506 | 518 | PF08784 | 0.439 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.386 |
LIG_SH2_GRB2like | 286 | 289 | PF00017 | 0.499 |
LIG_SH2_GRB2like | 30 | 33 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.389 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.396 |
LIG_SH2_SRC | 315 | 318 | PF00017 | 0.654 |
LIG_SH2_SRC | 355 | 358 | PF00017 | 0.517 |
LIG_SH2_SRC | 97 | 100 | PF00017 | 0.270 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.520 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.394 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.471 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.466 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.321 |
LIG_SUMO_SIM_anti_2 | 504 | 510 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 89 | 96 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 486 | 492 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 504 | 510 | PF11976 | 0.476 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.501 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.375 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.427 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.426 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.399 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.333 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.477 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.561 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.502 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.425 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.545 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.615 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.537 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.483 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.501 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.544 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.555 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.630 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.384 |
MOD_LATS_1 | 151 | 157 | PF00433 | 0.365 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.485 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.439 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.453 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.552 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.433 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.353 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.473 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.496 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.594 |
MOD_PK_1 | 252 | 258 | PF00069 | 0.322 |
MOD_PKA_1 | 104 | 110 | PF00069 | 0.354 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.482 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.525 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.460 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.548 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.360 |
MOD_PKB_1 | 20 | 28 | PF00069 | 0.455 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.452 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.389 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.380 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.309 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.473 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 101 | 107 | PF00179 | 0.278 |
MOD_SUMO_rev_2 | 510 | 519 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 527 | 532 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.681 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 415 | 418 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HR00 | Leptomonas seymouri | 41% | 100% |
A0A0N1I2Q7 | Leptomonas seymouri | 46% | 93% |
A0A1X0NYY7 | Trypanosomatidae | 44% | 70% |
A0A3Q8IJ32 | Leishmania donovani | 81% | 66% |
A0A422NAR5 | Trypanosoma rangeli | 46% | 69% |
A4H8M8 | Leishmania braziliensis | 96% | 100% |
A4H8N0 | Leishmania braziliensis | 51% | 70% |
A4HX01 | Leishmania infantum | 54% | 70% |
A4I0N5 | Leishmania infantum | 32% | 70% |
E9AGN8 | Leishmania infantum | 81% | 100% |
E9AGP0 | Leishmania infantum | 75% | 89% |
Q4QER4 | Leishmania major | 77% | 100% |
Q4QES0 | Leishmania major | 83% | 100% |
V5ANJ8 | Trypanosoma cruzi | 46% | 69% |