Electron Transport Chain (see tricarboxylic acid section for Complex II), electron transfer flavo-ubiquinone oxidoreductase
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. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0019866 | organelle inner membrane | 4 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0031966 | mitochondrial membrane | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3S5H5Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0022900 | electron transport chain | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004174 | electron-transferring-flavoprotein dehydrogenase activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009055 | electron transfer activity | 3 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016645 | oxidoreductase activity, acting on the CH-NH group of donors | 3 | 12 |
GO:0016649 | oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor | 4 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.387 |
CLV_MEL_PAP_1 | 219 | 225 | PF00089 | 0.465 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.402 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.502 |
DEG_SCF_FBW7_1 | 101 | 106 | PF00400 | 0.475 |
DOC_ANK_TNKS_1 | 328 | 335 | PF00023 | 0.285 |
DOC_CDC14_PxL_1 | 336 | 344 | PF14671 | 0.292 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 469 | 479 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 503 | 513 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 339 | 345 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.295 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.286 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.331 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 189 | 196 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.388 |
LIG_APCC_ABBAyCdc20_2 | 203 | 209 | PF00400 | 0.288 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.356 |
LIG_CSL_BTD_1 | 122 | 125 | PF09270 | 0.529 |
LIG_eIF4E_1 | 326 | 332 | PF01652 | 0.284 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.472 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.309 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.299 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.326 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.474 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.393 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.252 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.295 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.318 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.509 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.311 |
LIG_IBAR_NPY_1 | 296 | 298 | PF08397 | 0.311 |
LIG_Integrin_isoDGR_2 | 187 | 189 | PF01839 | 0.377 |
LIG_LIR_Apic_2 | 240 | 245 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 293 | 297 | PF02991 | 0.272 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 515 | 519 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 26 | 33 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 333 | 344 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.273 |
LIG_LYPXL_S_1 | 156 | 160 | PF13949 | 0.348 |
LIG_Pex14_1 | 4 | 8 | PF04695 | 0.614 |
LIG_Pex14_1 | 429 | 433 | PF04695 | 0.450 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.301 |
LIG_Pex14_2 | 423 | 427 | PF04695 | 0.332 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.274 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 294 | 297 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.309 |
LIG_SH2_NCK_1 | 380 | 384 | PF00017 | 0.337 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.362 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.145 |
LIG_SH2_STAT3 | 571 | 574 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.177 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.647 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.447 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.450 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.395 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.484 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.299 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.472 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.311 |
MOD_Cter_Amidation | 187 | 190 | PF01082 | 0.453 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.606 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.414 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.290 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.283 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.464 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.267 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.251 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.503 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.371 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.304 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.380 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.266 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.451 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.278 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.414 |
MOD_LATS_1 | 485 | 491 | PF00433 | 0.287 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.449 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.269 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.328 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.514 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.294 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.295 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.426 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.354 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.522 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.435 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.516 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.500 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.287 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.287 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.504 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.514 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.298 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.330 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.381 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.372 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.360 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.448 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.343 |
MOD_Plk_2-3 | 396 | 402 | PF00069 | 0.329 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.286 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.394 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.294 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.367 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.478 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.474 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.489 |
MOD_SUMO_rev_2 | 390 | 399 | PF00179 | 0.423 |
MOD_SUMO_rev_2 | 464 | 471 | PF00179 | 0.397 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU17 | Leptomonas seymouri | 81% | 98% |
A0A0S4J6T4 | Bodo saltans | 68% | 100% |
A0A1X0NPE8 | Trypanosomatidae | 71% | 100% |
A0A422N647 | Trypanosoma rangeli | 72% | 100% |
A4H510 | Leishmania braziliensis | 93% | 100% |
A4HT84 | Leishmania infantum | 100% | 100% |
C9ZUP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AL72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
O22854 | Arabidopsis thaliana | 50% | 91% |
P09820 | Rhizobium meliloti (strain 1021) | 24% | 100% |
P10331 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 24% | 100% |
P26484 | Azorhizobium caulinodans (strain ATCC 43989 / DSM 5975 / JCM 20966 / LMG 6465 / NBRC 14845 / NCIMB 13405 / ORS 571) | 25% | 100% |
P53572 | Azotobacter vinelandii | 23% | 100% |
P55931 | Sus scrofa | 54% | 93% |
P87111 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 48% | 91% |
P94132 | Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) | 48% | 100% |
Q08822 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 49% | 91% |
Q11190 | Caenorhabditis elegans | 53% | 96% |
Q16134 | Homo sapiens | 54% | 93% |
Q2KIG0 | Bos taurus | 54% | 93% |
Q337B8 | Oryza sativa subsp. japonica | 50% | 100% |
Q4QIN2 | Leishmania major | 98% | 100% |
Q53208 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 26% | 100% |
Q54XM6 | Dictyostelium discoideum | 51% | 95% |
Q5RDD3 | Pongo abelii | 54% | 93% |
Q6UPE1 | Rattus norvegicus | 54% | 93% |
Q921G7 | Mus musculus | 54% | 93% |
Q9HZP5 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 50% | 100% |
V5BTC8 | Trypanosoma cruzi | 71% | 100% |