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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AKH4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 8 |
GO:0006865 | amino acid transport | 5 | 8 |
GO:0015849 | organic acid transport | 5 | 8 |
GO:0051179 | localization | 1 | 8 |
GO:0051234 | establishment of localization | 2 | 8 |
GO:0071702 | organic substance transport | 4 | 8 |
GO:0071705 | nitrogen compound transport | 4 | 8 |
GO:0003333 | amino acid transmembrane transport | 5 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015711 | organic anion transport | 5 | 1 |
GO:0015804 | neutral amino acid transport | 6 | 1 |
GO:0032329 | serine transport | 6 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0046942 | carboxylic acid transport | 6 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
GO:0140300 | serine import into mitochondrion | 4 | 1 |
GO:1903825 | organic acid transmembrane transport | 3 | 1 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 1 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 1 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 1 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 1 |
GO:0015175 | neutral L-amino acid transmembrane transporter activity | 6 | 1 |
GO:0022889 | serine transmembrane transporter activity | 5 | 1 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.265 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.268 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.327 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.287 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.287 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.630 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.468 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.293 |
DOC_CYCLIN_RxL_1 | 27 | 38 | PF00134 | 0.487 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 106 | 115 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 261 | 264 | PF00134 | 0.283 |
DOC_CYCLIN_yCln2_LP_2 | 287 | 293 | PF00134 | 0.444 |
DOC_MAPK_DCC_7 | 252 | 261 | PF00069 | 0.283 |
DOC_MAPK_gen_1 | 283 | 291 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 252 | 261 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.397 |
DOC_MAPK_NFAT4_5 | 284 | 292 | PF00069 | 0.571 |
DOC_PP1_RVXF_1 | 273 | 280 | PF00149 | 0.470 |
DOC_PP1_RVXF_1 | 28 | 35 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.343 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.283 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.444 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.250 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 204 | 220 | PF00022 | 0.316 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.251 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.479 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.505 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.276 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.374 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.579 |
LIG_GBD_Chelix_1 | 296 | 304 | PF00786 | 0.343 |
LIG_IRF3_LxIS_1 | 151 | 158 | PF10401 | 0.268 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.486 |
LIG_MYND_1 | 93 | 97 | PF01753 | 0.487 |
LIG_PCNA_yPIPBox_3 | 242 | 254 | PF02747 | 0.244 |
LIG_PTB_Apo_2 | 129 | 136 | PF02174 | 0.244 |
LIG_PTB_Apo_2 | 265 | 272 | PF02174 | 0.343 |
LIG_PTB_Phospho_1 | 129 | 135 | PF10480 | 0.244 |
LIG_REV1ctd_RIR_1 | 277 | 288 | PF16727 | 0.470 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.343 |
LIG_SH2_SRC | 75 | 78 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.487 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.617 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.270 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.291 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.350 |
LIG_Sin3_3 | 187 | 194 | PF02671 | 0.468 |
LIG_SUMO_SIM_anti_2 | 295 | 301 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.343 |
LIG_TYR_ITIM | 195 | 200 | PF00017 | 0.343 |
MOD_CDC14_SPxK_1 | 46 | 49 | PF00782 | 0.505 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.244 |
MOD_CDK_SPxK_1 | 43 | 49 | PF00069 | 0.487 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.287 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.287 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.481 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.244 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.244 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.610 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.444 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.305 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.179 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.531 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.285 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.357 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.266 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.583 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.448 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.444 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.444 |
MOD_N-GLC_2 | 110 | 112 | PF02516 | 0.343 |
MOD_N-GLC_2 | 140 | 142 | PF02516 | 0.444 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.268 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.304 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.487 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.505 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.343 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.444 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.244 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.488 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.305 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.371 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.148 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.250 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.591 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.487 |
MOD_SUMO_rev_2 | 230 | 237 | PF00179 | 0.268 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.343 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P786 | Leptomonas seymouri | 76% | 100% |
A0A0N1I4E4 | Leptomonas seymouri | 29% | 100% |
A0A0S4IJR6 | Bodo saltans | 44% | 100% |
A0A1X0P3C3 | Trypanosomatidae | 29% | 100% |
A0A3R7KD90 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H4W1 | Leishmania donovani | 29% | 100% |
A0A3S5H5J2 | Leishmania donovani | 97% | 100% |
A4H380 | Leishmania braziliensis | 28% | 99% |
A4H4B2 | Leishmania braziliensis | 88% | 100% |
A4HRI0 | Leishmania infantum | 29% | 100% |
A4HSJ0 | Leishmania infantum | 97% | 100% |
A5A761 | Sus scrofa | 32% | 100% |
A6QP55 | Bos taurus | 32% | 100% |
A8E7G5 | Danio rerio | 27% | 100% |
B2LU20 | Ovis aries | 34% | 100% |
C9ZXK7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AC48 | Leishmania major | 29% | 99% |
E9AJE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 99% |
O13793 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
Q09201 | Caenorhabditis elegans | 31% | 100% |
Q12029 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q3T0M2 | Bos taurus | 27% | 100% |
Q4QJD4 | Leishmania major | 96% | 100% |
Q54NQ9 | Dictyostelium discoideum | 32% | 100% |
Q5E9M8 | Bos taurus | 34% | 100% |
Q5EA43 | Bos taurus | 31% | 100% |
Q5FC79 | Caenorhabditis elegans | 32% | 100% |
Q5RD16 | Pongo abelii | 33% | 100% |
Q63965 | Rattus norvegicus | 33% | 100% |
Q6P4A7 | Homo sapiens | 23% | 100% |
Q8CFD0 | Rattus norvegicus | 32% | 100% |
Q8TD22 | Homo sapiens | 32% | 100% |
Q91V61 | Mus musculus | 33% | 100% |
Q925N0 | Mus musculus | 32% | 100% |
Q925N2 | Mus musculus | 30% | 100% |
Q96NB2 | Homo sapiens | 31% | 100% |
Q99JR1 | Mus musculus | 33% | 100% |
Q9BWM7 | Homo sapiens | 32% | 100% |
Q9H9B4 | Homo sapiens | 32% | 100% |
Q9JHY2 | Rattus norvegicus | 33% | 100% |
Q9VN13 | Drosophila melanogaster | 29% | 100% |
Q9VVW3 | Drosophila melanogaster | 29% | 100% |
V5BCG0 | Trypanosoma cruzi | 28% | 100% |