Carbohydrate metabolism, phosphoglucomutase
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) | yes | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000287 | magnesium ion binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004614 | phosphoglucomutase 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 | 185 | 189 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.453 |
CLV_PCSK_FUR_1 | 99 | 103 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.378 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.655 |
DEG_SCF_FBW7_1 | 88 | 95 | PF00400 | 0.360 |
DOC_ANK_TNKS_1 | 100 | 107 | PF00023 | 0.504 |
DOC_CKS1_1 | 429 | 434 | PF01111 | 0.504 |
DOC_CKS1_1 | 89 | 94 | PF01111 | 0.359 |
DOC_MAPK_DCC_7 | 159 | 169 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 507 | 514 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 564 | 573 | PF00069 | 0.524 |
DOC_MAPK_RevD_3 | 569 | 583 | PF00069 | 0.553 |
DOC_PP1_RVXF_1 | 210 | 216 | PF00149 | 0.465 |
DOC_PP1_RVXF_1 | 509 | 515 | PF00149 | 0.378 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.378 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 313 | 316 | PF00568 | 0.379 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.378 |
DOC_SPAK_OSR1_1 | 311 | 315 | PF12202 | 0.408 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.359 |
DOC_WD40_RPTOR_TOS_1 | 182 | 188 | PF00400 | 0.531 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 59 | 69 | PF00244 | 0.402 |
LIG_APCC_ABBA_1 | 215 | 220 | PF00400 | 0.471 |
LIG_APCC_ABBA_1 | 534 | 539 | PF00400 | 0.378 |
LIG_BIR_III_4 | 103 | 107 | PF00653 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 411 | 419 | PF00928 | 0.359 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.343 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.349 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.337 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.427 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.500 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.471 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.373 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.626 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.357 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.560 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.466 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.417 |
LIG_LIR_Apic_2 | 23 | 28 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 495 | 499 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 411 | 422 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 456 | 465 | PF02991 | 0.452 |
LIG_LIR_LC3C_4 | 50 | 54 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 456 | 460 | PF02991 | 0.418 |
LIG_PCNA_PIPBox_1 | 437 | 446 | PF02747 | 0.432 |
LIG_Pex14_1 | 414 | 418 | PF04695 | 0.378 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.378 |
LIG_PTB_Apo_2 | 490 | 497 | PF02174 | 0.392 |
LIG_PTB_Phospho_1 | 490 | 496 | PF10480 | 0.392 |
LIG_Rb_LxCxE_1 | 389 | 409 | PF01857 | 0.361 |
LIG_SH2_NCK_1 | 457 | 461 | PF00017 | 0.475 |
LIG_SH2_SRC | 457 | 460 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.558 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 8 | 11 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.370 |
LIG_SH3_1 | 426 | 432 | PF00018 | 0.504 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.359 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.396 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.435 |
LIG_SUMO_SIM_anti_2 | 317 | 324 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 50 | 55 | PF11976 | 0.456 |
LIG_UBA3_1 | 417 | 425 | PF00899 | 0.504 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.504 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.413 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.312 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.378 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.485 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.378 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.542 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.531 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.423 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.512 |
MOD_Cter_Amidation | 105 | 108 | PF01082 | 0.387 |
MOD_Cter_Amidation | 580 | 583 | PF01082 | 0.588 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.359 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.394 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.449 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.268 |
MOD_GlcNHglycan | 458 | 463 | PF01048 | 0.495 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.378 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.378 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.378 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.480 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.492 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.419 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.471 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.465 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.347 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.576 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.378 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.500 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.359 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.359 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.480 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.432 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.343 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.501 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.475 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.426 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.378 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.359 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.380 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.456 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.504 |
MOD_NEK2_2 | 149 | 154 | PF00069 | 0.380 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.471 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.495 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.438 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.387 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.432 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.366 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.378 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.359 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.350 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.484 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.471 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.623 |
MOD_Plk_2-3 | 492 | 498 | PF00069 | 0.454 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.432 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.429 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.378 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.474 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.489 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.504 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.492 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.621 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMD7 | Leptomonas seymouri | 78% | 99% |
A0A0S4IYR2 | Bodo saltans | 60% | 100% |
A0A1X0NXZ7 | Trypanosomatidae | 64% | 100% |
A0A3Q8IBZ3 | Leishmania donovani | 100% | 100% |
A0A3S5IR70 | Trypanosoma rangeli | 61% | 100% |
A4HBR1 | Leishmania braziliensis | 90% | 100% |
D3ZVR9 | Rattus norvegicus | 43% | 100% |
E9AV30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O02606 | Paramecium tetraurelia | 48% | 100% |
O15820 | Entamoeba histolytica | 45% | 100% |
O18719 | Entamoeba dispar | 45% | 100% |
O49299 | Arabidopsis thaliana | 55% | 100% |
O74374 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 47% | 100% |
P00949 | Oryctolagus cuniculus | 49% | 100% |
P33401 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 45% | 100% |
P36871 | Homo sapiens | 49% | 100% |
P36938 | Escherichia coli (strain K12) | 27% | 100% |
P37012 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 45% | 100% |
P38569 | Komagataeibacter xylinus | 26% | 100% |
P38652 | Rattus norvegicus | 49% | 100% |
P39671 | Rhizobium radiobacter | 48% | 100% |
P47244 | Paramecium tetraurelia | 48% | 100% |
P57749 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 48% | 100% |
P93262 | Mesembryanthemum crystallinum | 55% | 100% |
P93804 | Zea mays | 55% | 100% |
P93805 | Zea mays | 55% | 100% |
Q08DP0 | Bos taurus | 50% | 100% |
Q15124 | Homo sapiens | 43% | 100% |
Q23919 | Dictyostelium discoideum | 48% | 100% |
Q4QCF1 | Leishmania major | 96% | 100% |
Q4R5E4 | Macaca fascicularis | 49% | 100% |
Q4WY53 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 48% | 100% |
Q8BZF8 | Mus musculus | 43% | 100% |
Q9D0F9 | Mus musculus | 49% | 100% |
Q9M4G4 | Solanum tuberosum | 54% | 100% |
Q9M4G5 | Solanum tuberosum | 50% | 93% |
Q9P931 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 49% | 100% |
Q9SCY0 | Arabidopsis thaliana | 50% | 95% |
Q9SGC1 | Arabidopsis thaliana | 56% | 100% |
Q9SM59 | Pisum sativum | 50% | 94% |
Q9SM60 | Pisum sativum | 54% | 100% |
Q9SMM0 | Brassica napus | 50% | 94% |
Q9SNX2 | Bromus inermis | 56% | 100% |
Q9VUY9 | Drosophila melanogaster | 49% | 100% |
Q9ZSQ4 | Populus tremula | 56% | 100% |
V5BMZ6 | Trypanosoma cruzi | 63% | 98% |