Uncharacterized Protein, Uncharacterized
| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0009331 | glycerol-3-phosphate dehydrogenase complex | 4 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
| GO:1990204 | oxidoreductase complex | 3 | 1 |
Related structures:
AlphaFold database: A4I4T2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006072 | glycerol-3-phosphate metabolic process | 5 | 1 |
| GO:0006793 | phosphorus metabolic process | 3 | 1 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0019637 | organophosphate metabolic process | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0046168 | glycerol-3-phosphate catabolic process | 5 | 1 |
| GO:0046434 | organophosphate catabolic process | 4 | 1 |
| GO:0052646 | alditol phosphate metabolic process | 4 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
| GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 1 |
| GO:0003824 | catalytic activity | 1 | 1 |
| GO:0005488 | binding | 1 | 1 |
| GO:0016491 | oxidoreductase activity | 2 | 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 |
| GO:0036094 | small molecule binding | 2 | 1 |
| GO:0047952 | glycerol-3-phosphate dehydrogenase [NAD(P)+] activity | 5 | 1 |
| GO:0051287 | NAD binding | 4 | 1 |
| GO:0097159 | organic cyclic compound binding | 2 | 1 |
| GO:1901265 | nucleoside phosphate binding | 3 | 1 |
| GO:1901363 | heterocyclic compound binding | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.569 |
| CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.497 |
| CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.618 |
| CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.593 |
| CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.578 |
| CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.702 |
| CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.578 |
| CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.617 |
| CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.550 |
| CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.718 |
| CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.489 |
| CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.446 |
| CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.560 |
| CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.449 |
| CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.565 |
| CLV_Separin_Metazoa | 546 | 550 | PF03568 | 0.512 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.473 |
| DEG_SCF_FBW7_1 | 127 | 134 | PF00400 | 0.585 |
| DEG_SCF_FBW7_1 | 163 | 169 | PF00400 | 0.549 |
| DEG_SCF_FBW7_1 | 277 | 284 | PF00400 | 0.673 |
| DOC_CKS1_1 | 163 | 168 | PF01111 | 0.515 |
| DOC_CKS1_1 | 259 | 264 | PF01111 | 0.580 |
| DOC_CKS1_1 | 278 | 283 | PF01111 | 0.479 |
| DOC_CYCLIN_yCln2_LP_2 | 32 | 35 | PF00134 | 0.450 |
| DOC_MAPK_gen_1 | 154 | 163 | PF00069 | 0.487 |
| DOC_PP1_RVXF_1 | 361 | 367 | PF00149 | 0.556 |
| DOC_PP1_RVXF_1 | 461 | 468 | PF00149 | 0.653 |
| DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.450 |
| DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.572 |
| DOC_PP2B_LxvP_1 | 439 | 442 | PF13499 | 0.543 |
| DOC_PP4_FxxP_1 | 2 | 5 | PF00568 | 0.471 |
| DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.744 |
| DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.637 |
| DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.548 |
| DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.488 |
| DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.668 |
| DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.515 |
| DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.616 |
| DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.590 |
| DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.725 |
| DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.553 |
| DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.460 |
| DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.494 |
| DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.567 |
| DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.725 |
| DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.634 |
| DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.505 |
| DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.622 |
| DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.455 |
| DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.614 |
| DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.364 |
| DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.463 |
| DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.468 |
| DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.450 |
| LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.555 |
| LIG_14-3-3_CanoR_1 | 497 | 506 | PF00244 | 0.356 |
| LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.426 |
| LIG_14-3-3_CanoR_1 | 565 | 573 | PF00244 | 0.534 |
| LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.601 |
| LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.443 |
| LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.491 |
| LIG_CSL_BTD_1 | 343 | 346 | PF09270 | 0.463 |
| LIG_CtBP_PxDLS_1 | 34 | 38 | PF00389 | 0.484 |
| LIG_CtBP_PxDLS_1 | 46 | 50 | PF00389 | 0.475 |
| LIG_deltaCOP1_diTrp_1 | 175 | 182 | PF00928 | 0.559 |
| LIG_FHA_1 | 188 | 194 | PF00498 | 0.450 |
| LIG_FHA_1 | 259 | 265 | PF00498 | 0.570 |
| LIG_FHA_1 | 343 | 349 | PF00498 | 0.465 |
| LIG_FHA_1 | 421 | 427 | PF00498 | 0.387 |
| LIG_FHA_1 | 450 | 456 | PF00498 | 0.537 |
| LIG_FHA_1 | 49 | 55 | PF00498 | 0.516 |
| LIG_FHA_1 | 498 | 504 | PF00498 | 0.339 |
| LIG_FHA_2 | 373 | 379 | PF00498 | 0.555 |
| LIG_FHA_2 | 537 | 543 | PF00498 | 0.639 |
| LIG_FHA_2 | 550 | 556 | PF00498 | 0.526 |
| LIG_LIR_Gen_1 | 214 | 225 | PF02991 | 0.451 |
| LIG_LIR_Gen_1 | 505 | 515 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.558 |
| LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.550 |
| LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.419 |
| LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.629 |
| LIG_PDZ_Class_1 | 577 | 582 | PF00595 | 0.651 |
| LIG_Pex14_2 | 217 | 221 | PF04695 | 0.510 |
| LIG_REV1ctd_RIR_1 | 37 | 45 | PF16727 | 0.450 |
| LIG_SH2_SRC | 170 | 173 | PF00017 | 0.453 |
| LIG_SH2_SRC | 9 | 12 | PF00017 | 0.450 |
| LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.504 |
| LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.401 |
| LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.559 |
| LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.510 |
| LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.654 |
| LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.621 |
| LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.450 |
| LIG_SH3_3 | 118 | 124 | PF00018 | 0.711 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.463 |
| LIG_SH3_3 | 500 | 506 | PF00018 | 0.540 |
| LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.531 |
| LIG_SUMO_SIM_par_1 | 260 | 267 | PF11976 | 0.513 |
| LIG_TRAF2_2 | 232 | 237 | PF00917 | 0.466 |
| LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.504 |
| MOD_CK1_1 | 125 | 131 | PF00069 | 0.610 |
| MOD_CK1_1 | 206 | 212 | PF00069 | 0.729 |
| MOD_CK1_1 | 276 | 282 | PF00069 | 0.613 |
| MOD_CK1_1 | 285 | 291 | PF00069 | 0.599 |
| MOD_CK1_1 | 293 | 299 | PF00069 | 0.630 |
| MOD_CK1_1 | 323 | 329 | PF00069 | 0.593 |
| MOD_CK1_1 | 402 | 408 | PF00069 | 0.556 |
| MOD_CK1_1 | 73 | 79 | PF00069 | 0.498 |
| MOD_CK1_1 | 98 | 104 | PF00069 | 0.733 |
| MOD_CK2_1 | 105 | 111 | PF00069 | 0.670 |
| MOD_CK2_1 | 252 | 258 | PF00069 | 0.747 |
| MOD_CK2_1 | 323 | 329 | PF00069 | 0.666 |
| MOD_CK2_1 | 536 | 542 | PF00069 | 0.593 |
| MOD_CK2_1 | 557 | 563 | PF00069 | 0.543 |
| MOD_Cter_Amidation | 461 | 464 | PF01082 | 0.631 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.736 |
| MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.765 |
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.623 |
| MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.450 |
| MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.461 |
| MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.546 |
| MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.750 |
| MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.716 |
| MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.471 |
| MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.489 |
| MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.638 |
| MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.494 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.779 |
| MOD_GSK3_1 | 123 | 130 | PF00069 | 0.663 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.499 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.617 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.454 |
| MOD_GSK3_1 | 254 | 261 | PF00069 | 0.691 |
| MOD_GSK3_1 | 273 | 280 | PF00069 | 0.337 |
| MOD_GSK3_1 | 281 | 288 | PF00069 | 0.607 |
| MOD_GSK3_1 | 289 | 296 | PF00069 | 0.530 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.491 |
| MOD_GSK3_1 | 449 | 456 | PF00069 | 0.450 |
| MOD_GSK3_1 | 498 | 505 | PF00069 | 0.475 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.748 |
| MOD_LATS_1 | 495 | 501 | PF00433 | 0.335 |
| MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.610 |
| MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.571 |
| MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.565 |
| MOD_N-GLC_2 | 387 | 389 | PF02516 | 0.390 |
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.529 |
| MOD_NEK2_1 | 282 | 287 | PF00069 | 0.527 |
| MOD_NEK2_1 | 294 | 299 | PF00069 | 0.546 |
| MOD_NEK2_1 | 39 | 44 | PF00069 | 0.452 |
| MOD_NEK2_1 | 399 | 404 | PF00069 | 0.547 |
| MOD_NEK2_1 | 498 | 503 | PF00069 | 0.485 |
| MOD_NEK2_1 | 511 | 516 | PF00069 | 0.463 |
| MOD_NEK2_1 | 577 | 582 | PF00069 | 0.643 |
| MOD_NEK2_1 | 96 | 101 | PF00069 | 0.561 |
| MOD_PKA_2 | 3 | 9 | PF00069 | 0.602 |
| MOD_PKA_2 | 367 | 373 | PF00069 | 0.437 |
| MOD_PKA_2 | 519 | 525 | PF00069 | 0.538 |
| MOD_PKA_2 | 536 | 542 | PF00069 | 0.698 |
| MOD_PKA_2 | 564 | 570 | PF00069 | 0.520 |
| MOD_Plk_1 | 273 | 279 | PF00069 | 0.548 |
| MOD_Plk_1 | 70 | 76 | PF00069 | 0.584 |
| MOD_Plk_1 | 92 | 98 | PF00069 | 0.681 |
| MOD_Plk_2-3 | 254 | 260 | PF00069 | 0.515 |
| MOD_Plk_4 | 131 | 137 | PF00069 | 0.543 |
| MOD_Plk_4 | 166 | 172 | PF00069 | 0.469 |
| MOD_Plk_4 | 290 | 296 | PF00069 | 0.675 |
| MOD_Plk_4 | 369 | 375 | PF00069 | 0.504 |
| MOD_Plk_4 | 399 | 405 | PF00069 | 0.581 |
| MOD_Plk_4 | 443 | 449 | PF00069 | 0.473 |
| MOD_Plk_4 | 50 | 56 | PF00069 | 0.492 |
| MOD_Plk_4 | 514 | 520 | PF00069 | 0.466 |
| MOD_Plk_4 | 75 | 81 | PF00069 | 0.493 |
| MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.724 |
| MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.619 |
| MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.504 |
| MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.629 |
| MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.455 |
| MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.609 |
| MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.372 |
| MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.462 |
| MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.461 |
| MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.443 |
| MOD_SUMO_rev_2 | 134 | 144 | PF00179 | 0.555 |
| TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.531 |
| TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.407 |
| TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.437 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P658 | Leptomonas seymouri | 55% | 100% |
| A0A0S4ITH1 | Bodo saltans | 23% | 100% |
| A0A1X0P970 | Trypanosomatidae | 33% | 100% |
| A0A3Q8IFB4 | Leishmania donovani | 100% | 100% |
| A0A422NEK6 | Trypanosoma rangeli | 32% | 100% |
| A4HHM3 | Leishmania braziliensis | 80% | 100% |
| E9AE85 | Leishmania major | 93% | 100% |
| E9ALK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |