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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
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: A0A3Q8IFB4
Term | Name | Level | Count |
---|---|---|---|
GO:0006072 | glycerol-3-phosphate metabolic process | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0046168 | glycerol-3-phosphate catabolic process | 5 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0052646 | alditol phosphate metabolic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 2 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0047952 | glycerol-3-phosphate dehydrogenase [NAD(P)+] activity | 5 | 1 |
GO:0051287 | NAD binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.528 |
CLV_Separin_Metazoa | 498 | 502 | PF03568 | 0.536 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.491 |
DEG_SCF_FBW7_1 | 115 | 121 | PF00400 | 0.536 |
DEG_SCF_FBW7_1 | 229 | 236 | PF00400 | 0.657 |
DEG_SCF_FBW7_1 | 79 | 86 | PF00400 | 0.584 |
DOC_CKS1_1 | 115 | 120 | PF01111 | 0.510 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.585 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.478 |
DOC_MAPK_gen_1 | 106 | 115 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 313 | 319 | PF00149 | 0.549 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.643 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 391 | 394 | PF13499 | 0.536 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 449 | 458 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.536 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.596 |
LIG_BRCT_BRCA1_1 | 407 | 411 | PF00533 | 0.490 |
LIG_CSL_BTD_1 | 295 | 298 | PF09270 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 127 | 134 | PF00928 | 0.593 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.579 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.473 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.564 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.479 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.380 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.536 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.338 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.550 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.642 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.554 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 457 | 467 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.569 |
LIG_PDZ_Class_1 | 529 | 534 | PF00595 | 0.626 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.466 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.600 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.546 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.730 |
LIG_SUMO_SIM_anti_2 | 27 | 33 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 212 | 219 | PF11976 | 0.476 |
LIG_TRAF2_2 | 184 | 189 | PF00917 | 0.460 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.508 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.649 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.587 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.686 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.553 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.571 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.566 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.721 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.611 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.759 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.706 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.576 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.572 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.681 |
MOD_Cter_Amidation | 413 | 416 | PF01082 | 0.608 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.654 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.713 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.246 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.638 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.595 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.702 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.429 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.481 |
MOD_GlcNHglycan | 494 | 498 | PF01048 | 0.652 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.490 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.746 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.781 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.481 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.608 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.691 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.276 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.565 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.533 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.459 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.754 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.487 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.791 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.673 |
MOD_LATS_1 | 447 | 453 | PF00433 | 0.334 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.595 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.570 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.621 |
MOD_N-GLC_2 | 339 | 341 | PF02516 | 0.373 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.507 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.429 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.507 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.500 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.481 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.419 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.560 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.605 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.426 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.519 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.335 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.619 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.579 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.517 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.689 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.644 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.478 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.491 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.678 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.487 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.468 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.567 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.475 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.473 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.543 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.474 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.546 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.599 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.360 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.486 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.447 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.430 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.740 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.628 |
MOD_SUMO_rev_2 | 86 | 96 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_1 | 212 | 217 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P658 | Leptomonas seymouri | 55% | 100% |
A0A0S4ITH1 | Bodo saltans | 23% | 100% |
A0A1X0P970 | Trypanosomatidae | 34% | 100% |
A0A422NEK6 | Trypanosoma rangeli | 32% | 100% |
A4HHM3 | Leishmania braziliensis | 79% | 100% |
A4I4T2 | Leishmania infantum | 100% | 100% |
C9ZLH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AE85 | Leishmania major | 93% | 100% |
E9ALK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |