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: 40 |
NetGPI | no | yes: 0, no: 40 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 26 |
GO:0005794 | Golgi apparatus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
Related structures:
AlphaFold database: A4HX01
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 39 |
GO:0016740 | transferase activity | 2 | 39 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.430 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 529 | 537 | PF00400 | 0.336 |
DEG_APCC_DBOX_1 | 87 | 95 | PF00400 | 0.595 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.255 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.332 |
DOC_MAPK_DCC_7 | 459 | 467 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 368 | 377 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 99 | 108 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 370 | 379 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 449 | 456 | PF00069 | 0.724 |
DOC_MAPK_MEF2A_6 | 591 | 598 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 28 | 35 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 739 | 746 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 771 | 778 | PF00149 | 0.457 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 705 | 708 | PF13499 | 0.466 |
DOC_PP4_FxxP_1 | 537 | 540 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 159 | 163 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 334 | 344 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 409 | 418 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 504 | 513 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 595 | 599 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 699 | 708 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.564 |
LIG_14-3-3_CterR_2 | 780 | 785 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.652 |
LIG_Actin_WH2_2 | 399 | 414 | PF00022 | 0.360 |
LIG_Actin_WH2_2 | 603 | 620 | PF00022 | 0.489 |
LIG_BIR_III_4 | 429 | 433 | PF00653 | 0.534 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 553 | 557 | PF00533 | 0.549 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.251 |
LIG_deltaCOP1_diTrp_1 | 771 | 777 | PF00928 | 0.381 |
LIG_DLG_GKlike_1 | 643 | 650 | PF00625 | 0.366 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.302 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.449 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.474 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.254 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.439 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.583 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.392 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.419 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.452 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.425 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.604 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.597 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.555 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.354 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.500 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.502 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.608 |
LIG_LIR_Apic_2 | 535 | 540 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 757 | 761 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 763 | 772 | PF02991 | 0.568 |
LIG_LIR_LC3C_4 | 728 | 733 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 715 | 720 | PF02991 | 0.491 |
LIG_MYND_1 | 418 | 422 | PF01753 | 0.512 |
LIG_PCNA_yPIPBox_3 | 30 | 42 | PF02747 | 0.370 |
LIG_PCNA_yPIPBox_3 | 58 | 69 | PF02747 | 0.424 |
LIG_PTB_Apo_2 | 182 | 189 | PF02174 | 0.469 |
LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.535 |
LIG_PTB_Apo_2 | 288 | 295 | PF02174 | 0.351 |
LIG_PTB_Phospho_1 | 182 | 188 | PF10480 | 0.472 |
LIG_RPA_C_Fungi | 730 | 742 | PF08784 | 0.453 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.465 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.486 |
LIG_SH2_GRB2like | 183 | 186 | PF00017 | 0.589 |
LIG_SH2_PTP2 | 399 | 402 | PF00017 | 0.331 |
LIG_SH2_SRC | 571 | 574 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 632 | 636 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 619 | 622 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.378 |
LIG_SH3_2 | 691 | 696 | PF14604 | 0.482 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.381 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.388 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.606 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.569 |
LIG_SH3_3 | 663 | 669 | PF00018 | 0.542 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.461 |
LIG_SH3_3 | 753 | 759 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 728 | 734 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 104 | 109 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 710 | 716 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 728 | 734 | PF11976 | 0.354 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.577 |
LIG_TRAF2_1 | 570 | 573 | PF00917 | 0.529 |
LIG_TYR_ITIM | 3 | 8 | PF00017 | 0.536 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.471 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.474 |
LIG_WW_3 | 303 | 307 | PF00397 | 0.475 |
MOD_CDC14_SPxK_1 | 303 | 306 | PF00782 | 0.472 |
MOD_CDK_SPK_2 | 390 | 395 | PF00069 | 0.473 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.467 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.615 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.440 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.311 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.500 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.512 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.606 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.458 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.515 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.547 |
MOD_CK2_1 | 661 | 667 | PF00069 | 0.422 |
MOD_CMANNOS | 774 | 777 | PF00535 | 0.487 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.604 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.616 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.647 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.412 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.478 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.396 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.374 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.462 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.526 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.557 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.339 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.592 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.661 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.588 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.507 |
MOD_LATS_1 | 142 | 148 | PF00433 | 0.497 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.478 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.488 |
MOD_N-GLC_2 | 468 | 470 | PF02516 | 0.621 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.606 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.631 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.328 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.354 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.417 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.696 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.400 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.415 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.480 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.346 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.391 |
MOD_NEK2_2 | 634 | 639 | PF00069 | 0.347 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.570 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.336 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.569 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.566 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.457 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.429 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.499 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.594 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.549 |
MOD_PKB_1 | 368 | 376 | PF00069 | 0.301 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.234 |
MOD_Plk_1 | 606 | 612 | PF00069 | 0.424 |
MOD_Plk_2-3 | 264 | 270 | PF00069 | 0.404 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.639 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.583 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.457 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.439 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.443 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.372 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.643 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.446 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.492 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.399 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.444 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.483 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.484 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.605 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 270 | 280 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 419 | 428 | PF00179 | 0.641 |
MOD_SUMO_rev_2 | 455 | 460 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 734 | 743 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 751 | 756 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 765 | 768 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 777 | 780 | PF00400 | 0.428 |
TRG_NES_CRM1_1 | 697 | 710 | PF08389 | 0.432 |
TRG_NLS_MonoExtC_3 | 638 | 643 | PF00514 | 0.359 |
TRG_PTS1 | 782 | 785 | PF00515 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 55% | 100% |
A0A0S4JNL6 | Bodo saltans | 28% | 72% |
A0A1X0NYY7 | Trypanosomatidae | 39% | 99% |
A0A3Q8IAD3 | Leishmania donovani | 100% | 80% |
A0A3Q8IAF8 | Leishmania donovani | 52% | 82% |
A0A3Q8IAK8 | Leishmania donovani | 54% | 81% |
A0A3Q8IJ32 | Leishmania donovani | 54% | 95% |
A0A3S5H6Y1 | Leishmania donovani | 53% | 83% |
A0A3S7WTZ8 | Leishmania donovani | 52% | 76% |
A0A3S7WU13 | Leishmania donovani | 53% | 84% |
A0A422NAR5 | Trypanosoma rangeli | 39% | 99% |
A4H8M5 | Leishmania braziliensis | 50% | 100% |
A4H8M6 | Leishmania braziliensis | 54% | 87% |
A4H8M7 | Leishmania braziliensis | 55% | 100% |
A4H8N0 | Leishmania braziliensis | 44% | 100% |
A4H8N1 | Leishmania braziliensis | 82% | 100% |
A4HWZ5 | Leishmania infantum | 54% | 100% |
A4HWZ6 | Leishmania infantum | 50% | 100% |
A4HWZ8 | Leishmania infantum | 55% | 100% |
A4HX00 | Leishmania infantum | 53% | 100% |
A4HX05 | Leishmania infantum | 57% | 81% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AGP0 | Leishmania infantum | 56% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AQR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AQR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AQR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AQR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QER2 | Leishmania major | 93% | 100% |
Q4QER3 | Leishmania major | 53% | 100% |
Q4QER4 | Leishmania major | 57% | 94% |
Q4QER5 | Leishmania major | 54% | 100% |
Q4QER6 | Leishmania major | 54% | 100% |
Q4QER7 | Leishmania major | 55% | 100% |
Q4QER8 | Leishmania major | 55% | 100% |
Q4QER9 | Leishmania major | 55% | 100% |
Q4QES0 | Leishmania major | 54% | 100% |
V5ANJ8 | Trypanosoma cruzi | 39% | 98% |