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: 0 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HPH2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 11 |
GO:0009057 | macromolecule catabolic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044248 | cellular catabolic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 11 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901575 | organic substance catabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0019899 | enzyme binding | 3 | 11 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 11 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.227 |
DEG_MDM2_SWIB_1 | 17 | 24 | PF02201 | 0.436 |
DEG_SCF_FBW7_2 | 393 | 400 | PF00400 | 0.473 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.493 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.473 |
DOC_CYCLIN_RxL_1 | 319 | 328 | PF00134 | 0.484 |
DOC_CYCLIN_RxL_1 | 687 | 697 | PF00134 | 0.438 |
DOC_MAPK_FxFP_2 | 315 | 318 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 466 | 476 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 518 | 526 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 407 | 414 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 468 | 476 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 677 | 684 | PF00069 | 0.499 |
DOC_MAPK_NFAT4_5 | 677 | 685 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 516 | 523 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.521 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.493 |
DOC_USP7_UBL2_3 | 607 | 611 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 129 | 139 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 38 | 42 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 452 | 461 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 601 | 610 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 638 | 643 | PF00244 | 0.514 |
LIG_APCC_ABBA_1 | 366 | 371 | PF00400 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.521 |
LIG_EH1_1 | 546 | 554 | PF00400 | 0.521 |
LIG_EVH1_2 | 472 | 476 | PF00568 | 0.493 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.572 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.462 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.464 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.525 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.502 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.510 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.364 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.452 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.432 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.399 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.486 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.521 |
LIG_Integrin_isoDGR_2 | 516 | 518 | PF01839 | 0.242 |
LIG_LIR_Apic_2 | 312 | 318 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 13 | 19 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 346 | 356 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 475 | 481 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 579 | 589 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 475 | 479 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.444 |
LIG_MLH1_MIPbox_1 | 174 | 178 | PF16413 | 0.493 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.448 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.428 |
LIG_Pex14_2 | 599 | 603 | PF04695 | 0.366 |
LIG_Pex14_2 | 89 | 93 | PF04695 | 0.530 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.460 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.438 |
LIG_PTB_Phospho_1 | 108 | 114 | PF10480 | 0.460 |
LIG_PTB_Phospho_1 | 236 | 242 | PF10480 | 0.438 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.521 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.493 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.484 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.528 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.411 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.446 |
LIG_SH2_GRB2like | 370 | 373 | PF00017 | 0.493 |
LIG_SH2_GRB2like | 489 | 492 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.521 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.568 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 290 | 296 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 562 | 567 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.484 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.518 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.493 |
LIG_TYR_ITIM | 656 | 661 | PF00017 | 0.368 |
LIG_UBA3_1 | 145 | 150 | PF00899 | 0.493 |
LIG_UBA3_1 | 323 | 331 | PF00899 | 0.460 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.495 |
MOD_CDC14_SPxK_1 | 674 | 677 | PF00782 | 0.493 |
MOD_CDK_SPxK_1 | 671 | 677 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.521 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.506 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.490 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.465 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.558 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.504 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.615 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.442 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.463 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.452 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.521 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.572 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.521 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.549 |
MOD_Cter_Amidation | 516 | 519 | PF01082 | 0.259 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.253 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.321 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.284 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.321 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.476 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.506 |
MOD_GlcNHglycan | 622 | 626 | PF01048 | 0.471 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.461 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.371 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.558 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.477 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.493 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.485 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.484 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.501 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.496 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.540 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.459 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.447 |
MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.455 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.333 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.465 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.434 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.490 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.473 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.459 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.504 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.428 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.517 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.479 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.521 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.466 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.427 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.481 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.473 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.429 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.508 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.438 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.463 |
MOD_Plk_1 | 559 | 565 | PF00069 | 0.565 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.501 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.421 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.465 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.542 |
MOD_Plk_2-3 | 249 | 255 | PF00069 | 0.493 |
MOD_Plk_2-3 | 652 | 658 | PF00069 | 0.473 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.475 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.550 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.497 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.465 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.438 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.492 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.473 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.495 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.493 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.456 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.435 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.431 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.527 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.479 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.474 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.493 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.441 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.473 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.533 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 285 | 288 | PF00179 | 0.493 |
MOD_SUMO_for_1 | 32 | 35 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 459 | 467 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 674 | 682 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_1 | 475 | 480 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_1 | 689 | 694 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 410 | 415 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.570 |
TRG_NES_CRM1_1 | 235 | 249 | PF08389 | 0.521 |
TRG_NLS_MonoExtC_3 | 7 | 13 | PF00514 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 518 | 523 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 648 | 652 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9C6 | Leptomonas seymouri | 66% | 100% |
A0A1X0NKJ9 | Trypanosomatidae | 27% | 100% |
A0A1X0NXD6 | Trypanosomatidae | 20% | 95% |
A0A3R7LZU1 | Trypanosoma rangeli | 28% | 99% |
A0A3S7XB28 | Leishmania donovani | 89% | 100% |
A2A432 | Mus musculus | 20% | 73% |
A4ID94 | Leishmania infantum | 89% | 100% |
D0A3I2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AT84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
O14122 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 96% |
Q09760 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 90% |
Q4Q1B3 | Leishmania major | 88% | 100% |
Q8LGH4 | Arabidopsis thaliana | 21% | 89% |
Q9ZVH4 | Arabidopsis thaliana | 20% | 96% |
V5B0B0 | Trypanosoma cruzi | 28% | 100% |