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: E9ALK0
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 | 0.430 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.521 |
CLV_Separin_Metazoa | 498 | 502 | PF03568 | 0.447 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.433 |
DEG_SCF_FBW7_1 | 115 | 121 | PF00400 | 0.411 |
DEG_SCF_FBW7_1 | 229 | 236 | PF00400 | 0.512 |
DEG_SCF_FBW7_1 | 79 | 86 | PF00400 | 0.478 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.424 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.491 |
DOC_CKS1_1 | 115 | 120 | PF01111 | 0.479 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.572 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.407 |
DOC_MAPK_gen_1 | 107 | 115 | PF00069 | 0.349 |
DOC_PP1_RVXF_1 | 313 | 319 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.619 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.434 |
DOC_PP2B_LxvP_1 | 391 | 394 | PF13499 | 0.406 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.436 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.559 |
LIG_BRCT_BRCA1_1 | 407 | 411 | PF00533 | 0.433 |
LIG_deltaCOP1_diTrp_1 | 127 | 134 | PF00928 | 0.460 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.399 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.443 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.415 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.474 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.490 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.493 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.444 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.326 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.502 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.623 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.416 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.644 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.507 |
LIG_GBD_Chelix_1 | 187 | 195 | PF00786 | 0.271 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 457 | 467 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.607 |
LIG_NRBOX | 191 | 197 | PF00104 | 0.323 |
LIG_PDZ_Class_1 | 529 | 534 | PF00595 | 0.588 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.452 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.587 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.639 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 27 | 33 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 212 | 219 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 44 | 51 | PF11976 | 0.563 |
LIG_TRAF2_2 | 184 | 189 | PF00917 | 0.355 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.483 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.659 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.568 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.658 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.544 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.709 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.532 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.535 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.715 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.690 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.546 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.651 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.549 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.558 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.517 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.593 |
MOD_Cter_Amidation | 413 | 416 | PF01082 | 0.542 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.636 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.639 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.283 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.705 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.726 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.658 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.393 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.467 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.432 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.710 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.389 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.445 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.593 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.492 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.321 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.512 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.309 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.545 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.592 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.734 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.439 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.461 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.430 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.711 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.424 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.612 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.774 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.636 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.453 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.587 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.642 |
MOD_N-GLC_2 | 339 | 341 | PF02516 | 0.316 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.488 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.484 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.472 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.524 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.414 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.369 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.515 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.586 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.443 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.446 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.386 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.674 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.512 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.383 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.608 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.538 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.428 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.456 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.429 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.368 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.494 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.603 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.438 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.441 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.567 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.475 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.433 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.427 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.573 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.330 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.473 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.396 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.366 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.732 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.628 |
MOD_SUMO_rev_2 | 86 | 96 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 212 | 217 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P658 | Leptomonas seymouri | 55% | 100% |
A0A0S4ITH1 | Bodo saltans | 24% | 100% |
A0A1X0P970 | Trypanosomatidae | 39% | 100% |
A0A3Q8IFB4 | Leishmania donovani | 90% | 100% |
A0A422NEK6 | Trypanosoma rangeli | 33% | 100% |
A4HHM3 | Leishmania braziliensis | 79% | 100% |
A4I4T2 | Leishmania infantum | 91% | 92% |
C9ZLH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AE85 | Leishmania major | 90% | 100% |