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: 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:0005739 | mitochondrion | 5 | 2 |
GO:0005750 | mitochondrial respiratory chain complex III | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0045275 | respiratory chain complex III | 4 | 2 |
GO:0070069 | cytochrome complex | 3 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 2 |
GO:0098803 | respiratory chain complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1902495 | transmembrane transporter complex | 3 | 2 |
GO:1990204 | oxidoreductase complex | 3 | 2 |
GO:1990351 | transporter complex | 2 | 2 |
GO:0016020 | membrane | 2 | 9 |
Related structures:
AlphaFold database: Q4QIT8
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 2 |
GO:0006122 | mitochondrial electron transport, ubiquinol to cytochrome c | 7 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009060 | aerobic respiration | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015980 | energy derivation by oxidation of organic compounds | 4 | 2 |
GO:0019646 | aerobic electron transport chain | 6 | 2 |
GO:0022900 | electron transport chain | 4 | 2 |
GO:0022904 | respiratory electron transport chain | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0045333 | cellular respiration | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009055 | electron transfer activity | 3 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0020037 | heme binding | 4 | 12 |
GO:0046906 | tetrapyrrole binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.303 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.301 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.447 |
DOC_PP1_RVXF_1 | 213 | 220 | PF00149 | 0.300 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.316 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.300 |
DOC_PP4_MxPP_1 | 174 | 177 | PF00568 | 0.300 |
DOC_SPAK_OSR1_1 | 20 | 24 | PF12202 | 0.335 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.421 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 205 | 212 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 36 | 45 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.273 |
LIG_Actin_WH2_2 | 143 | 160 | PF00022 | 0.336 |
LIG_Actin_WH2_2 | 189 | 207 | PF00022 | 0.335 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.544 |
LIG_BIR_III_4 | 81 | 85 | PF00653 | 0.335 |
LIG_deltaCOP1_diTrp_1 | 12 | 21 | PF00928 | 0.423 |
LIG_deltaCOP1_diTrp_1 | 22 | 29 | PF00928 | 0.300 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.289 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.300 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.300 |
LIG_IBAR_NPY_1 | 164 | 166 | PF08397 | 0.300 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 53 | 61 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.300 |
LIG_MYND_1 | 155 | 159 | PF01753 | 0.312 |
LIG_Pex14_1 | 163 | 167 | PF04695 | 0.300 |
LIG_PTB_Apo_2 | 161 | 168 | PF02174 | 0.300 |
LIG_SH2_GRB2like | 14 | 17 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 39 | 43 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 73 | 77 | PF00017 | 0.300 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.316 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.316 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.294 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.300 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.298 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.300 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.300 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.300 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.300 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.300 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.493 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.300 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.316 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.441 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.300 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.300 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.300 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.447 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.302 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.300 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.427 |
MOD_SUMO_rev_2 | 64 | 69 | PF00179 | 0.277 |
TRG_DiLeu_BaEn_4 | 64 | 70 | PF01217 | 0.300 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.421 |
TRG_ER_diLys_1 | 255 | 258 | PF00400 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF2 | Leptomonas seymouri | 95% | 100% |
A0A0S4IRH2 | Bodo saltans | 82% | 100% |
A0A1X0NKV6 | Trypanosomatidae | 90% | 100% |
A0A3S7WPP0 | Leishmania donovani | 100% | 100% |
A0A422NTC0 | Trypanosoma rangeli | 90% | 100% |
A4H4U9 | Leishmania braziliensis | 97% | 100% |
A4HT63 | Leishmania infantum | 100% | 100% |
C9ZUW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 91% | 85% |
D5ANZ4 | Rhodobacter capsulatus (strain ATCC BAA-309 / NBRC 16581 / SB1003) | 29% | 92% |
E9AL16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
O59680 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 45% | 84% |
P00125 | Bos taurus | 45% | 79% |
P07142 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 48% | 78% |
P07143 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 83% |
P08574 | Homo sapiens | 45% | 79% |
P0CY49 | Rhodobacter capsulatus | 29% | 92% |
P20114 | Euglena gracilis | 42% | 100% |
P23135 | Rhodospirillum rubrum | 38% | 95% |
P25076 | Solanum tuberosum | 42% | 81% |
P29610 | Solanum tuberosum | 41% | 99% |
P81379 | Blastochloris viridis | 33% | 91% |
Q00988 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 46% | 88% |
Q02760 | Cereibacter sphaeroides | 28% | 91% |
Q54D07 | Dictyostelium discoideum | 43% | 94% |
Q9D0M3 | Mus musculus | 43% | 79% |
Q9FKS5 | Arabidopsis thaliana | 42% | 84% |
Q9LK29 | Arabidopsis thaliana | 39% | 84% |
V5D9C0 | Trypanosoma cruzi | 92% | 100% |