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: 15 |
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AGN8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.763 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.748 |
CLV_PCSK_FUR_1 | 9 | 13 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.646 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.741 |
DOC_CYCLIN_yCln2_LP_2 | 52 | 58 | PF00134 | 0.371 |
DOC_MAPK_DCC_7 | 137 | 146 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 137 | 146 | PF00069 | 0.694 |
DOC_MAPK_gen_1 | 45 | 56 | PF00069 | 0.371 |
DOC_MAPK_HePTP_8 | 165 | 177 | PF00069 | 0.762 |
DOC_MAPK_MEF2A_6 | 168 | 177 | PF00069 | 0.777 |
DOC_MAPK_MEF2A_6 | 251 | 258 | PF00069 | 0.641 |
DOC_MAPK_MEF2A_6 | 47 | 56 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 391 | 398 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.371 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.748 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.225 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 255 | 259 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 276 | 284 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 425 | 429 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.243 |
LIG_Actin_WH2_2 | 95 | 113 | PF00022 | 0.460 |
LIG_BIR_III_2 | 90 | 94 | PF00653 | 0.736 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.603 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.552 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.566 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.682 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.552 |
LIG_LIR_Apic_2 | 409 | 413 | PF02991 | 0.568 |
LIG_LIR_Apic_2 | 423 | 429 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 118 | 125 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.549 |
LIG_LIR_LC3C_4 | 380 | 385 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.743 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.399 |
LIG_MAD2 | 276 | 284 | PF02301 | 0.509 |
LIG_PTB_Apo_2 | 139 | 146 | PF02174 | 0.701 |
LIG_PTB_Phospho_1 | 139 | 145 | PF10480 | 0.704 |
LIG_RPA_C_Fungi | 382 | 394 | PF08784 | 0.523 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.321 |
LIG_SH2_GRB2like | 145 | 148 | PF00017 | 0.685 |
LIG_SH2_NCK_1 | 417 | 421 | PF00017 | 0.327 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.763 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.496 |
LIG_SH2_SRC | 417 | 420 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.321 |
LIG_SH2_STAT3 | 288 | 291 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.822 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.618 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.577 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.593 |
LIG_SH3_CIN85_PxpxPR_1 | 3 | 8 | PF14604 | 0.521 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.501 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.514 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.495 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.602 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.571 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.698 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.533 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.563 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.531 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.618 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.696 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.234 |
MOD_LATS_1 | 10 | 16 | PF00433 | 0.529 |
MOD_LATS_1 | 43 | 49 | PF00433 | 0.234 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.537 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.438 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.486 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.515 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.564 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.742 |
MOD_NEK2_2 | 38 | 43 | PF00069 | 0.257 |
MOD_PK_1 | 299 | 305 | PF00069 | 0.467 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.234 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.550 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.257 |
MOD_Plk_2-3 | 290 | 296 | PF00069 | 0.465 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.730 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.599 |
MOD_SUMO_rev_2 | 386 | 395 | PF00179 | 0.595 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.822 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.749 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 49% | 73% |
A4H8M6 | Leishmania braziliensis | 81% | 100% |
A4H8M8 | Leishmania braziliensis | 79% | 96% |
E9AGP0 | Leishmania infantum | 93% | 69% |