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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0070469 | respirasome | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9ATM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009060 | aerobic respiration | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010230 | alternative respiration | 7 | 1 |
GO:0015980 | energy derivation by oxidation of organic compounds | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0045333 | cellular respiration | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0009916 | alternative oxidase activity | 5 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 9 |
GO:0016679 | oxidoreductase activity, acting on diphenols and related substances as donors | 3 | 9 |
GO:0016682 | oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor | 4 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 428 | 432 | PF00656 | 0.411 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.259 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.593 |
CLV_PCSK_PC7_1 | 156 | 162 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.529 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.390 |
DOC_CKS1_1 | 424 | 429 | PF01111 | 0.390 |
DOC_CYCLIN_RxL_1 | 472 | 483 | PF00134 | 0.499 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 134 | 141 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.725 |
DOC_MAPK_RevD_3 | 404 | 419 | PF00069 | 0.390 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.501 |
DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.552 |
DOC_PP1_RVXF_1 | 6 | 12 | PF00149 | 0.574 |
DOC_PP4_MxPP_1 | 82 | 85 | PF00568 | 0.642 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.731 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 134 | 138 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 18 | 28 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 203 | 207 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 417 | 425 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 88 | 98 | PF00244 | 0.541 |
LIG_BIR_III_2 | 431 | 435 | PF00653 | 0.390 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.713 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.569 |
LIG_eIF4E_1 | 279 | 285 | PF01652 | 0.397 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.560 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.438 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.501 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.643 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.408 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.301 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.544 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.533 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.500 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.533 |
LIG_HCF-1_HBM_1 | 230 | 233 | PF13415 | 0.398 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.702 |
LIG_LYPXL_S_1 | 285 | 289 | PF13949 | 0.391 |
LIG_LYPXL_yS_3 | 286 | 289 | PF13949 | 0.525 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.348 |
LIG_NRBOX | 266 | 272 | PF00104 | 0.492 |
LIG_REV1ctd_RIR_1 | 156 | 165 | PF16727 | 0.314 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.747 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.733 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.402 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.569 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.445 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.598 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 259 | 264 | PF11976 | 0.348 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 437 | 443 | PF11976 | 0.519 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.560 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.598 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.438 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.357 |
LIG_UBA3_1 | 476 | 484 | PF00899 | 0.586 |
LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.488 |
LIG_WW_1 | 64 | 67 | PF00397 | 0.516 |
MOD_CDK_SPxK_1 | 100 | 106 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 388 | 395 | PF00069 | 0.415 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.706 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.457 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.346 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.430 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.746 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.457 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.364 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.575 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.422 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.442 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.372 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.394 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.438 |
MOD_DYRK1A_RPxSP_1 | 388 | 392 | PF00069 | 0.415 |
MOD_DYRK1A_RPxSP_1 | 423 | 427 | PF00069 | 0.201 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.457 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.486 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.394 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.702 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.702 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.373 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.719 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.699 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.438 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.423 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.336 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.502 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.350 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.416 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.706 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.407 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.777 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.556 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.643 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.419 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.488 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.228 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.408 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.715 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.479 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.444 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.412 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.346 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.669 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.735 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.494 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.492 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.201 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.438 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.708 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.616 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.492 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.298 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.357 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.445 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.390 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.479 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.201 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.257 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.442 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.357 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.354 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.282 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.357 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.257 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.358 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.492 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.592 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.507 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.438 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.438 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.201 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.332 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.471 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.228 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.201 |
TRG_DiLeu_BaEn_1 | 236 | 241 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.201 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.629 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.415 |
TRG_NES_CRM1_1 | 259 | 272 | PF08389 | 0.422 |
TRG_NES_CRM1_1 | 457 | 469 | PF08389 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 456 | 461 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P770 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IWB1 | Leishmania donovani | 87% | 100% |
A4HPV5 | Leishmania braziliensis | 69% | 100% |
A4IDL7 | Leishmania infantum | 87% | 100% |
D0A4A4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q0X6 | Leishmania major | 85% | 100% |
V5BQ82 | Trypanosoma cruzi | 32% | 100% |