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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 8 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005947 | mitochondrial alpha-ketoglutarate dehydrogenase complex | 4 | 1 |
GO:0030062 | mitochondrial tricarboxylic acid cycle enzyme complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045239 | tricarboxylic acid cycle enzyme complex | 3 | 1 |
GO:0045240 | dihydrolipoyl dehydrogenase complex | 4 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990204 | oxidoreductase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HM44
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006520 | amino acid metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007584 | response to nutrient | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009063 | amino acid catabolic process | 4 | 1 |
GO:0009081 | branched-chain amino acid metabolic process | 4 | 1 |
GO:0009083 | branched-chain amino acid catabolic process | 5 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0009991 | response to extracellular stimulus | 3 | 1 |
GO:0016054 | organic acid catabolic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0031667 | response to nutrient levels | 4 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046395 | carboxylic acid catabolic process | 5 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003863 | 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) activity | 5 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0016624 | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor | 4 | 8 |
GO:0016903 | oxidoreductase activity, acting on the aldehyde or oxo group of donors | 3 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.254 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.606 |
DOC_ANK_TNKS_1 | 239 | 246 | PF00023 | 0.515 |
DOC_CKS1_1 | 158 | 163 | PF01111 | 0.373 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 338 | 344 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 295 | 302 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 43 | 51 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.360 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.454 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.437 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.441 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.451 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.437 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.343 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.470 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.522 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.567 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.392 |
LIG_LIR_Apic_2 | 128 | 132 | PF02991 | 0.437 |
LIG_LIR_Apic_2 | 230 | 235 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 29 | 36 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.437 |
LIG_PDZ_Class_2 | 361 | 366 | PF00595 | 0.420 |
LIG_Pex14_2 | 77 | 81 | PF04695 | 0.437 |
LIG_PTB_Apo_2 | 225 | 232 | PF02174 | 0.465 |
LIG_PTB_Phospho_1 | 225 | 231 | PF10480 | 0.469 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.355 |
LIG_SH2_GRB2like | 179 | 182 | PF00017 | 0.385 |
LIG_SH2_PTP2 | 129 | 132 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 91 | 94 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.319 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.433 |
LIG_SUMO_SIM_anti_2 | 273 | 278 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 66 | 74 | PF11976 | 0.525 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.470 |
LIG_UBA3_1 | 356 | 361 | PF00899 | 0.436 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.444 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.451 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.492 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.490 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.511 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.497 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.619 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.298 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.431 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.251 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.237 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.633 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.637 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.437 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.525 |
MOD_N-GLC_2 | 181 | 183 | PF02516 | 0.173 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.492 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.469 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.593 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.437 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.469 |
MOD_PK_1 | 22 | 28 | PF00069 | 0.640 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.437 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.437 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.443 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.437 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.437 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.447 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.446 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.385 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.440 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.437 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.451 |
MOD_SUMO_rev_2 | 192 | 200 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 209 | 219 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.278 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M5 | Leptomonas seymouri | 88% | 100% |
A0A0N0P8J5 | Leptomonas seymouri | 33% | 100% |
A0A0S4J2J6 | Bodo saltans | 32% | 100% |
A0A1X0NJN2 | Trypanosomatidae | 78% | 99% |
A0A1X0NY97 | Trypanosomatidae | 34% | 100% |
A0A3Q8IJ06 | Leishmania donovani | 94% | 100% |
A0A3S7WZ91 | Leishmania donovani | 32% | 100% |
A0A422N7P1 | Trypanosoma rangeli | 73% | 100% |
A0A422NGI4 | Trypanosoma rangeli | 32% | 100% |
A2CI50 | Chlorokybus atmophyticus | 36% | 100% |
A4HEH1 | Leishmania braziliensis | 33% | 100% |
A4I1L9 | Leishmania infantum | 32% | 100% |
A4IAQ6 | Leishmania infantum | 94% | 100% |
C9ZK62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A2G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 99% |
E9AEI2 | Leishmania major | 95% | 100% |
E9AXQ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B5P3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
G0RYE0 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 33% | 96% |
O34591 | Bacillus subtilis (strain 168) | 38% | 100% |
O44451 | Caenorhabditis elegans | 35% | 100% |
O64688 | Arabidopsis thaliana | 31% | 90% |
O66113 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 33% | 79% |
P09061 | Pseudomonas putida | 47% | 100% |
P0A0A1 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 43% | 100% |
P0A0A2 | Staphylococcus aureus (strain MW2) | 43% | 100% |
P0A0A3 | Staphylococcus aureus | 43% | 100% |
P11177 | Homo sapiens | 33% | 100% |
P11966 | Bos taurus | 34% | 100% |
P21839 | Bos taurus | 54% | 93% |
P21874 | Geobacillus stearothermophilus | 43% | 100% |
P21882 | Bacillus subtilis (strain 168) | 41% | 100% |
P21953 | Homo sapiens | 55% | 93% |
P26269 | Ascaris suum | 33% | 100% |
P27746 | Cupriavidus necator (strain ATCC 17699 / DSM 428 / KCTC 22496 / NCIMB 10442 / H16 / Stanier 337) | 38% | 100% |
P32473 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P35488 | Acholeplasma laidlawii | 44% | 100% |
P35738 | Rattus norvegicus | 58% | 94% |
P37941 | Bacillus subtilis (strain 168) | 42% | 100% |
P47515 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 39% | 100% |
P49432 | Rattus norvegicus | 33% | 100% |
P51266 | Porphyra purpurea | 38% | 100% |
P52904 | Pisum sativum | 36% | 100% |
P55573 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 24% | 100% |
P75391 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 41% | 100% |
P99063 | Staphylococcus aureus (strain N315) | 43% | 100% |
P9WF02 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 55% | 78% |
P9WIS0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 43% | 100% |
P9WIS1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 43% | 100% |
Q09171 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
Q0J0H4 | Oryza sativa subsp. japonica | 37% | 97% |
Q10G39 | Oryza sativa subsp. japonica | 33% | 92% |
Q1ACL0 | Chara vulgaris | 34% | 100% |
Q1RJX3 | Rickettsia bellii (strain RML369-C) | 35% | 100% |
Q1XDM1 | Neopyropia yezoensis | 38% | 100% |
Q2QM55 | Oryza sativa subsp. japonica | 33% | 94% |
Q32RM2 | Zygnema circumcarinatum | 34% | 100% |
Q32RS0 | Staurastrum punctulatum | 34% | 100% |
Q38799 | Arabidopsis thaliana | 36% | 100% |
Q4Q9R8 | Leishmania major | 32% | 100% |
Q4UKQ7 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 36% | 100% |
Q55FN7 | Dictyostelium discoideum | 62% | 99% |
Q5HGZ0 | Staphylococcus aureus (strain COL) | 43% | 100% |
Q5HQ75 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 42% | 100% |
Q5RE79 | Pongo abelii | 33% | 100% |
Q5SLR3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 47% | 100% |
Q68XA8 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 35% | 100% |
Q6ABX8 | Leifsonia xyli subsp. xyli (strain CTCB07) | 42% | 100% |
Q6B8T1 | Gracilaria tenuistipitata var. liui | 38% | 100% |
Q6GAC0 | Staphylococcus aureus (strain MSSA476) | 43% | 100% |
Q6GHZ1 | Staphylococcus aureus (strain MRSA252) | 43% | 100% |
Q6P3A8 | Mus musculus | 58% | 94% |
Q6Z1G7 | Oryza sativa subsp. japonica | 37% | 98% |
Q72GU2 | Thermus thermophilus (strain ATCC BAA-163 / DSM 7039 / HB27) | 46% | 100% |
Q7K5K3 | Drosophila melanogaster | 34% | 100% |
Q85FX1 | Cyanidioschyzon merolae (strain NIES-3377 / 10D) | 34% | 100% |
Q86HX0 | Dictyostelium discoideum | 36% | 100% |
Q8CPN2 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 42% | 100% |
Q8MA03 | Chaetosphaeridium globosum | 36% | 100% |
Q92IS2 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 36% | 100% |
Q9C6Z3 | Arabidopsis thaliana | 32% | 90% |
Q9D051 | Mus musculus | 33% | 100% |
Q9I1M1 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 45% | 100% |
Q9LDY2 | Arabidopsis thaliana | 56% | 100% |
Q9MUR4 | Mesostigma viride | 34% | 100% |
Q9R9N4 | Rhizobium meliloti (strain 1021) | 36% | 80% |
Q9SAV3 | Arabidopsis thaliana | 57% | 100% |
Q9TLS3 | Cyanidium caldarium | 34% | 100% |
Q9ZDR3 | Rickettsia prowazekii (strain Madrid E) | 36% | 100% |
V5BIR9 | Trypanosoma cruzi | 75% | 99% |
V5DIT8 | Trypanosoma cruzi | 32% | 100% |