Tricarboxylic acid cycle, Succinate dehydrogenase (SDH5)
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: 11 |
NetGPI | no | yes: 0, no: 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: A0A3S7X2A6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 66 | 74 | PF00400 | 0.486 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.594 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 |
DEG_SCF_FBW7_1 | 363 | 369 | PF00400 | 0.599 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.631 |
DOC_CKS1_1 | 282 | 287 | PF01111 | 0.509 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.676 |
DOC_CYCLIN_RxL_1 | 405 | 415 | PF00134 | 0.381 |
DOC_CYCLIN_RxL_1 | 447 | 456 | PF00134 | 0.365 |
DOC_CYCLIN_RxL_1 | 457 | 466 | PF00134 | 0.356 |
DOC_MAPK_gen_1 | 455 | 464 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 97 | 105 | PF00069 | 0.321 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.637 |
DOC_SPAK_OSR1_1 | 98 | 102 | PF12202 | 0.430 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.393 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.552 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 477 | 483 | PF00244 | 0.511 |
LIG_Actin_WH2_2 | 1 | 18 | PF00022 | 0.628 |
LIG_AP2alpha_1 | 277 | 281 | PF02296 | 0.423 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.586 |
LIG_CaM_IQ_9 | 242 | 257 | PF13499 | 0.475 |
LIG_CaM_NSCaTE_8 | 152 | 159 | PF13499 | 0.426 |
LIG_eIF4E_1 | 447 | 453 | PF01652 | 0.382 |
LIG_eIF4E_1 | 459 | 465 | PF01652 | 0.515 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.412 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.454 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.413 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.349 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.394 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.414 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.418 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.350 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.585 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.490 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.638 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.515 |
LIG_GBD_Chelix_1 | 403 | 411 | PF00786 | 0.448 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.136 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.405 |
LIG_LRP6_Inhibitor_1 | 24 | 30 | PF00058 | 0.461 |
LIG_NRBOX | 337 | 343 | PF00104 | 0.579 |
LIG_PCNA_yPIPBox_3 | 26 | 40 | PF02747 | 0.503 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.423 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.394 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.478 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.660 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.467 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.423 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.349 |
LIG_UBA3_1 | 111 | 115 | PF00899 | 0.397 |
MOD_CDK_SPxxK_3 | 483 | 490 | PF00069 | 0.640 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.448 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.339 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.618 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.455 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.424 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.458 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.464 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.412 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.352 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.524 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.454 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.594 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.534 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.507 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.524 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.511 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.467 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.534 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.434 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.475 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.499 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.458 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.523 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.474 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.465 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.492 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.512 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.454 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.366 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.499 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.450 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.323 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.397 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.551 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.408 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.575 |
MOD_NEK2_2 | 159 | 164 | PF00069 | 0.421 |
MOD_NEK2_2 | 377 | 382 | PF00069 | 0.609 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.458 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.374 |
MOD_PK_1 | 347 | 353 | PF00069 | 0.599 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.585 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.473 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.441 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.405 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.599 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.493 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.443 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.587 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.391 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.495 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.533 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.614 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.457 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 219 | 222 | PF00179 | 0.576 |
MOD_SUMO_for_1 | 314 | 317 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 107 | 117 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 135 | 144 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 177 | 182 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 333 | 338 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 469 | 475 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_4 | 259 | 265 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 470 | 474 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E1 | Leptomonas seymouri | 79% | 100% |
A0A0S4IX38 | Bodo saltans | 30% | 95% |
A0A1X0P156 | Trypanosomatidae | 45% | 100% |
A0A422NRS1 | Trypanosoma rangeli | 43% | 100% |
A4HH97 | Leishmania braziliensis | 87% | 100% |
A4I4E3 | Leishmania infantum | 100% | 100% |
C9ZL20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ADU3 | Leishmania major | 98% | 100% |
E9ALY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5BR79 | Trypanosoma cruzi | 45% | 100% |