Oxidoreductase, aldo/keto reductase
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I250
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0004032 | alditol:NADP+ 1-oxidoreductase activity | 7 | 1 |
GO:0004033 | aldo-keto reductase (NADP) activity | 5 | 1 |
GO:0008106 | alcohol dehydrogenase (NADP+) activity | 6 | 1 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 1 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.608 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.619 |
DOC_CYCLIN_RxL_1 | 526 | 535 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 405 | 412 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 541 | 549 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 37 | 44 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 77 | 86 | PF00069 | 0.448 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.605 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.515 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.451 |
DOC_PP4_MxPP_1 | 80 | 83 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.787 |
LIG_14-3-3_CanoR_1 | 108 | 114 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 529 | 539 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 69 | 78 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 81 | 98 | PF00022 | 0.493 |
LIG_BIR_III_4 | 277 | 281 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.584 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.543 |
LIG_eIF4E_1 | 259 | 265 | PF01652 | 0.539 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.596 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.546 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.346 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.475 |
LIG_MYND_1 | 93 | 97 | PF01753 | 0.483 |
LIG_PCNA_PIPBox_1 | 536 | 545 | PF02747 | 0.584 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.477 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.598 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.485 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.437 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 560 | 563 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.687 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.725 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.652 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.485 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.482 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.619 |
LIG_UBA3_1 | 248 | 254 | PF00899 | 0.530 |
LIG_UBA3_1 | 291 | 300 | PF00899 | 0.619 |
MOD_CDK_SPxxK_3 | 413 | 420 | PF00069 | 0.486 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.504 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.486 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.776 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.717 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.501 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.656 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.696 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.675 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.752 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.768 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.363 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.346 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.337 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.783 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.549 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.738 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.518 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.473 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.441 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.480 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.514 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.672 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.464 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.766 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.439 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.677 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.562 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.653 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.620 |
MOD_LATS_1 | 435 | 441 | PF00433 | 0.507 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.588 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.664 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.487 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.581 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.661 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.546 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.444 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.651 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.442 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.618 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.663 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.618 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.536 |
MOD_PKA_1 | 149 | 155 | PF00069 | 0.526 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.516 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.490 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.524 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.477 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.517 |
MOD_PKB_1 | 147 | 155 | PF00069 | 0.525 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.502 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.435 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.493 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.723 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.332 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.453 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.782 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.583 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 427 | 432 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.508 |
TRG_NES_CRM1_1 | 246 | 261 | PF08389 | 0.563 |
TRG_NLS_MonoExtC_3 | 252 | 258 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4R8 | Leptomonas seymouri | 58% | 100% |
A0A3S7WZZ0 | Leishmania donovani | 99% | 100% |
A4HEX6 | Leishmania braziliensis | 77% | 100% |
E9AYA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q973 | Leishmania major | 92% | 100% |