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. | yes | yes: 75 |
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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0005794 | Golgi apparatus | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
Related structures:
AlphaFold database: E9AGP0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 24 |
GO:0016740 | transferase activity | 2 | 24 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.609 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.627 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.583 |
CLV_PCSK_FUR_1 | 272 | 276 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.528 |
DOC_CKS1_1 | 359 | 364 | PF01111 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 242 | 248 | PF00134 | 0.328 |
DOC_MAPK_DCC_7 | 327 | 336 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 235 | 244 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 327 | 336 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 67 | 76 | PF00069 | 0.508 |
DOC_MAPK_HePTP_8 | 355 | 367 | PF00069 | 0.659 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 358 | 367 | PF00069 | 0.675 |
DOC_MAPK_MEF2A_6 | 441 | 448 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.511 |
DOC_PP1_RVXF_1 | 581 | 588 | PF00149 | 0.417 |
DOC_PP2B_LxvP_1 | 242 | 245 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.575 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.379 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 201 | 211 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 445 | 449 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 466 | 474 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 53 | 57 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 615 | 619 | PF00244 | 0.657 |
LIG_Actin_WH2_2 | 141 | 158 | PF00022 | 0.415 |
LIG_Actin_WH2_2 | 23 | 40 | PF00022 | 0.709 |
LIG_BIR_III_2 | 280 | 284 | PF00653 | 0.542 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.623 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.474 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.625 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.457 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.506 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.300 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.406 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.526 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.609 |
LIG_LIR_Apic_2 | 599 | 603 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 613 | 619 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 605 | 614 | PF02991 | 0.599 |
LIG_LIR_LC3C_4 | 570 | 575 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.520 |
LIG_MAD2 | 466 | 474 | PF02301 | 0.609 |
LIG_PTB_Apo_2 | 329 | 336 | PF02174 | 0.489 |
LIG_PTB_Apo_2 | 76 | 83 | PF02174 | 0.493 |
LIG_PTB_Phospho_1 | 329 | 335 | PF10480 | 0.566 |
LIG_PTB_Phospho_1 | 76 | 82 | PF10480 | 0.497 |
LIG_REV1ctd_RIR_1 | 216 | 226 | PF16727 | 0.315 |
LIG_RPA_C_Fungi | 572 | 584 | PF08784 | 0.430 |
LIG_SH2_GRB2like | 335 | 338 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 77 | 80 | PF00017 | 0.616 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.696 |
LIG_SH2_SRC | 421 | 424 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.208 |
LIG_SH2_STAT3 | 478 | 481 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.438 |
LIG_SH3_2 | 197 | 202 | PF14604 | 0.448 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.456 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.514 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 135 | 142 | PF11976 | 0.507 |
LIG_SUMO_SIM_anti_2 | 570 | 576 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 552 | 558 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 570 | 576 | PF11976 | 0.490 |
LIG_SxIP_EBH_1 | 189 | 202 | PF03271 | 0.401 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.632 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.525 |
MOD_CDK_SPK_2 | 257 | 262 | PF00069 | 0.442 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.453 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.696 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.335 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.541 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.562 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.447 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.566 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.543 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.609 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.419 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.689 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.493 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.582 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.604 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.427 |
MOD_LATS_1 | 36 | 42 | PF00433 | 0.522 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.471 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.484 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.423 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.485 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.392 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.567 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.677 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.528 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.416 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.484 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.390 |
MOD_PK_1 | 489 | 495 | PF00069 | 0.557 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.324 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.333 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.637 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.465 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.542 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.477 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.350 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.484 |
MOD_Plk_2-3 | 480 | 486 | PF00069 | 0.620 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.475 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.414 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.601 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.421 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.492 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.701 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.372 |
MOD_SUMO_rev_2 | 576 | 585 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 593 | 598 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.717 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 351 | 353 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 66 | 69 | PF00400 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 46% | 100% |
A0A1X0NYY7 | Trypanosomatidae | 44% | 78% |
A0A3Q8IJ32 | Leishmania donovani | 88% | 75% |
A0A422NAR5 | Trypanosoma rangeli | 45% | 78% |
A4H8M5 | Leishmania braziliensis | 81% | 69% |
A4H8M6 | Leishmania braziliensis | 75% | 96% |
A4H8M7 | Leishmania braziliensis | 76% | 100% |
A4H8N0 | Leishmania braziliensis | 52% | 79% |
A4HWZ6 | Leishmania infantum | 100% | 68% |
A4HWZ8 | Leishmania infantum | 100% | 100% |
A4HX01 | Leishmania infantum | 56% | 100% |
A4I0N5 | Leishmania infantum | 32% | 79% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 66% |
E9AGN8 | Leishmania infantum | 93% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 67% |
Q4QER4 | Leishmania major | 92% | 100% |
Q4QER5 | Leishmania major | 82% | 100% |
Q4QER6 | Leishmania major | 82% | 100% |
Q4QER7 | Leishmania major | 92% | 100% |
Q4QER9 | Leishmania major | 92% | 100% |
Q4QES0 | Leishmania major | 81% | 100% |
V5ANJ8 | Trypanosoma cruzi | 45% | 77% |