Carbohydrate metabolism, Phosphoacetylglucosamine mutase-like
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: 5 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HTA8
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 11 |
GO:0006040 | amino sugar metabolic process | 4 | 11 |
GO:0006047 | UDP-N-acetylglucosamine metabolic process | 4 | 11 |
GO:0006048 | UDP-N-acetylglucosamine biosynthetic process | 5 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009225 | nucleotide-sugar metabolic process | 4 | 11 |
GO:0009226 | nucleotide-sugar biosynthetic process | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0046349 | amino sugar biosynthetic process | 5 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0006041 | glucosamine metabolic process | 6 | 1 |
GO:1901071 | glucosamine-containing compound metabolic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000287 | magnesium ion binding | 5 | 6 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004610 | phosphoacetylglucosamine mutase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0016868 | intramolecular transferase activity, phosphotransferases | 4 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 540 | 544 | PF00656 | 0.313 |
CLV_MEL_PAP_1 | 59 | 65 | PF00089 | 0.451 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.332 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.332 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.716 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.376 |
DOC_CYCLIN_RxL_1 | 489 | 500 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 58 | PF00134 | 0.348 |
DOC_MAPK_gen_1 | 355 | 363 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 508 | 517 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 344 | 351 | PF00149 | 0.336 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.348 |
DOC_PP4_FxxP_1 | 235 | 238 | PF00568 | 0.367 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.378 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.267 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 62 | 66 | PF00244 | 0.395 |
LIG_Actin_WH2_2 | 11 | 26 | PF00022 | 0.526 |
LIG_Actin_WH2_2 | 171 | 187 | PF00022 | 0.467 |
LIG_Actin_WH2_2 | 56 | 72 | PF00022 | 0.341 |
LIG_APCC_ABBA_1 | 433 | 438 | PF00400 | 0.358 |
LIG_APCC_ABBA_1 | 569 | 574 | PF00400 | 0.313 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 117 | 122 | PF00928 | 0.380 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.477 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.368 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.371 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.313 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.426 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.472 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.491 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.487 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.457 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.312 |
LIG_IBAR_NPY_1 | 98 | 100 | PF08397 | 0.457 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 156 | 162 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 369 | 380 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 500 | 509 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.329 |
LIG_LYPXL_yS_3 | 192 | 195 | PF13949 | 0.545 |
LIG_MAD2 | 346 | 354 | PF02301 | 0.493 |
LIG_MLH1_MIPbox_1 | 16 | 20 | PF16413 | 0.512 |
LIG_Pex14_1 | 501 | 505 | PF04695 | 0.313 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.521 |
LIG_Rb_pABgroove_1 | 346 | 354 | PF01858 | 0.493 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.455 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.375 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.352 |
LIG_SH2_GRB2like | 221 | 224 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 397 | 400 | PF00017 | 0.350 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.386 |
LIG_SH2_SRC | 397 | 400 | PF00017 | 0.350 |
LIG_SH2_SRC | 572 | 575 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.485 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.527 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.446 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.505 |
LIG_SUMO_SIM_anti_2 | 389 | 395 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.508 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.456 |
LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.371 |
LIG_UBA3_1 | 370 | 378 | PF00899 | 0.453 |
LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.489 |
MOD_CDK_SPxxK_3 | 523 | 530 | PF00069 | 0.333 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.527 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.452 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.567 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.527 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.346 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.451 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.421 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.464 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.560 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.313 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.457 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.313 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.313 |
MOD_CMANNOS | 119 | 122 | PF00535 | 0.424 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.430 |
MOD_DYRK1A_RPxSP_1 | 531 | 535 | PF00069 | 0.282 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.530 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.409 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.540 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.555 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.487 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.313 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.457 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.501 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.608 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.487 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.520 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.519 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.482 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.416 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.460 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.336 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.350 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.462 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.421 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.575 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.428 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.511 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.511 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.667 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.478 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.427 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.528 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.340 |
MOD_NEK2_2 | 280 | 285 | PF00069 | 0.362 |
MOD_NEK2_2 | 68 | 73 | PF00069 | 0.398 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.613 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.361 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.430 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.379 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.490 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.506 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.365 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.424 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.313 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.427 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.401 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.456 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.424 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.461 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.536 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.498 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.458 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.253 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.334 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.410 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.353 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.508 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.455 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.486 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.469 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.333 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.267 |
MOD_SUMO_for_1 | 51 | 54 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 353 | 361 | PF00179 | 0.501 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.341 |
TRG_NES_CRM1_1 | 22 | 36 | PF08389 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 470 | 475 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5G0 | Leptomonas seymouri | 53% | 100% |
A0A0S4KHH8 | Bodo saltans | 36% | 100% |
A0A1X0NPH2 | Trypanosomatidae | 44% | 99% |
A0A3R7KD29 | Trypanosoma rangeli | 45% | 98% |
A0A3S5H601 | Leishmania donovani | 100% | 100% |
A4H3S0 | Leishmania braziliensis | 84% | 100% |
C9ZUL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9AL97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F1RQM2 | Sus scrofa | 38% | 100% |
O95394 | Homo sapiens | 37% | 100% |
P38628 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P57750 | Arabidopsis thaliana | 35% | 100% |
Q09687 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
Q09770 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
Q4QIK7 | Leishmania major | 93% | 100% |
Q5Z1H8 | Nocardia farcinica (strain IFM 10152) | 23% | 100% |
Q6ZDQ1 | Oryza sativa subsp. japonica | 35% | 100% |
Q7V349 | Prochlorococcus marinus subsp. pastoris (strain CCMP1986 / NIES-2087 / MED4) | 23% | 100% |
Q8SSL7 | Encephalitozoon cuniculi (strain GB-M1) | 32% | 100% |
Q9CYR6 | Mus musculus | 36% | 100% |
Q9P4V2 | Candida albicans | 34% | 100% |
V5B892 | Trypanosoma cruzi | 43% | 98% |