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: 125 |
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: 32 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 41 |
NetGPI | no | yes: 0, no: 41 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 28 |
GO:0016020 | membrane | 2 | 20 |
Related structures:
AlphaFold database: Q4QER4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 38 |
GO:0016740 | transferase activity | 2 | 38 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 679 | 683 | PF00656 | 0.401 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.643 |
CLV_PCSK_FUR_1 | 288 | 292 | PF00082 | 0.541 |
CLV_PCSK_FUR_1 | 361 | 365 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.589 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.615 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.494 |
DOC_CKS1_1 | 448 | 453 | PF01111 | 0.632 |
DOC_CYCLIN_yCln2_LP_2 | 331 | 337 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 669 | 675 | PF00134 | 0.410 |
DOC_MAPK_DCC_7 | 416 | 425 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 156 | 165 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 324 | 333 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 416 | 425 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 82 | 91 | PF00069 | 0.540 |
DOC_MAPK_HePTP_8 | 444 | 456 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 447 | 456 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 512 | 519 | PF00069 | 0.624 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 618 | 621 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.527 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 142 | 146 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 246 | 256 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 516 | 520 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 537 | 545 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 686 | 690 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 71 | 75 | PF00244 | 0.551 |
LIG_Actin_WH2_2 | 112 | 129 | PF00022 | 0.642 |
LIG_Actin_WH2_2 | 230 | 247 | PF00022 | 0.417 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.518 |
LIG_eIF4E_1 | 232 | 238 | PF01652 | 0.489 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.432 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.447 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.643 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.468 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.708 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.470 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.602 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.304 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.470 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.495 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.539 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 670 | 674 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 684 | 690 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 239 | 247 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 397 | 407 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 676 | 685 | PF02991 | 0.575 |
LIG_LIR_LC3C_4 | 641 | 646 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.529 |
LIG_MAD2 | 537 | 545 | PF02301 | 0.576 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.478 |
LIG_PTB_Apo_2 | 418 | 425 | PF02174 | 0.475 |
LIG_PTB_Phospho_1 | 165 | 171 | PF10480 | 0.484 |
LIG_PTB_Phospho_1 | 418 | 424 | PF10480 | 0.503 |
LIG_REV1ctd_RIR_1 | 305 | 315 | PF16727 | 0.312 |
LIG_SH2_GRB2like | 166 | 169 | PF00017 | 0.619 |
LIG_SH2_GRB2like | 23 | 26 | PF00017 | 0.528 |
LIG_SH2_GRB2like | 424 | 427 | PF00017 | 0.508 |
LIG_SH2_SRC | 453 | 456 | PF00017 | 0.542 |
LIG_SH2_SRC | 492 | 495 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.223 |
LIG_SH2_STAT3 | 549 | 552 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.561 |
LIG_SH3_2 | 286 | 291 | PF14604 | 0.447 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.466 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 224 | 231 | PF11976 | 0.527 |
LIG_SUMO_SIM_anti_2 | 641 | 647 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 623 | 629 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 641 | 647 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 87 | 92 | PF11976 | 0.540 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.634 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.534 |
MOD_CDK_SPK_2 | 346 | 351 | PF00069 | 0.461 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.643 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.438 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.546 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.304 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.491 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.563 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.458 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.604 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.576 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.595 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.691 |
MOD_GlcNHglycan | 205 | 209 | PF01048 | 0.569 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.650 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.418 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.517 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.590 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.572 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.593 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.451 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.368 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.603 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.390 |
MOD_LATS_1 | 125 | 131 | PF00433 | 0.480 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.502 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.639 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.454 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.642 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.576 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.517 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.456 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.412 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.645 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.562 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.417 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.451 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.486 |
MOD_NEK2_2 | 523 | 528 | PF00069 | 0.515 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.391 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.520 |
MOD_PK_1 | 560 | 566 | PF00069 | 0.563 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.570 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.446 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.496 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.622 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.554 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.591 |
MOD_PKB_1 | 156 | 164 | PF00069 | 0.517 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.523 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.454 |
MOD_Plk_2-3 | 551 | 557 | PF00069 | 0.629 |
MOD_Plk_2-3 | 64 | 70 | PF00069 | 0.686 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.599 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.446 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.385 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.468 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.440 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.587 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.510 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.613 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.629 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.521 |
TRG_DiLeu_BaEn_1 | 664 | 669 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 592 | 595 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 47% | 100% |
A0A1X0NYY7 | Trypanosomatidae | 45% | 87% |
A0A3Q8IAD3 | Leishmania donovani | 57% | 71% |
A0A3Q8IAF8 | Leishmania donovani | 87% | 72% |
A0A3Q8IAK8 | Leishmania donovani | 89% | 71% |
A0A3Q8IJ32 | Leishmania donovani | 79% | 83% |
A0A3S5H6Y1 | Leishmania donovani | 85% | 73% |
A0A3S7WTZ8 | Leishmania donovani | 67% | 67% |
A0A3S7WU13 | Leishmania donovani | 79% | 73% |
A0A422NAR5 | Trypanosoma rangeli | 47% | 87% |
A4H8M5 | Leishmania braziliensis | 81% | 76% |
A4H8M6 | Leishmania braziliensis | 77% | 100% |
A4H8M7 | Leishmania braziliensis | 75% | 75% |
A4H8N0 | Leishmania braziliensis | 50% | 88% |
A4H8N1 | Leishmania braziliensis | 55% | 71% |
A4HWZ5 | Leishmania infantum | 79% | 73% |
A4HWZ6 | Leishmania infantum | 84% | 76% |
A4HWZ8 | Leishmania infantum | 92% | 75% |
A4HX00 | Leishmania infantum | 67% | 67% |
A4HX01 | Leishmania infantum | 57% | 88% |
A4HX05 | Leishmania infantum | 88% | 72% |
A4HZW0 | Leishmania infantum | 30% | 73% |
A4I0N5 | Leishmania infantum | 32% | 88% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 74% |
E9AGP0 | Leishmania infantum | 92% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 80% |
E9AQR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 70% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 74% |
E9AQR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 73% |
E9AQR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9AQR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 70% |
Q4QER2 | Leishmania major | 57% | 100% |
Q4QER3 | Leishmania major | 71% | 100% |
Q4QER5 | Leishmania major | 84% | 81% |
Q4QER6 | Leishmania major | 84% | 81% |
Q4QER7 | Leishmania major | 95% | 80% |
Q4QER8 | Leishmania major | 100% | 72% |
Q4QER9 | Leishmania major | 97% | 75% |
Q4QES0 | Leishmania major | 84% | 85% |
V5ANJ8 | Trypanosoma cruzi | 47% | 86% |