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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HK97
Term | Name | Level | Count |
---|---|---|---|
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 14 | 20 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 42 | 50 | PF00400 | 0.438 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.410 |
DOC_CKS1_1 | 37 | 42 | PF01111 | 0.408 |
DOC_CYCLIN_RxL_1 | 56 | 64 | PF00134 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 250 | 256 | PF00134 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 287 | 293 | PF00134 | 0.483 |
DOC_MAPK_gen_1 | 18 | 26 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 210 | 218 | PF00069 | 0.379 |
DOC_MAPK_RevD_3 | 164 | 179 | PF00069 | 0.255 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.559 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.296 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.584 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 59 | 68 | PF00244 | 0.435 |
LIG_Actin_WH2_2 | 87 | 104 | PF00022 | 0.484 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.306 |
LIG_CSL_BTD_1 | 164 | 167 | PF09270 | 0.402 |
LIG_CtBP_PxDLS_1 | 130 | 134 | PF00389 | 0.384 |
LIG_EVH1_1 | 37 | 41 | PF00568 | 0.406 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.503 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.295 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.260 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.498 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.460 |
LIG_NRBOX | 45 | 51 | PF00104 | 0.439 |
LIG_PTB_Apo_2 | 153 | 160 | PF02174 | 0.240 |
LIG_PTB_Phospho_1 | 153 | 159 | PF10480 | 0.242 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.507 |
LIG_SH3_2 | 38 | 43 | PF14604 | 0.411 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.569 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.458 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.439 |
LIG_SH3_CIN85_PxpxPR_1 | 38 | 43 | PF14604 | 0.411 |
LIG_SUMO_SIM_par_1 | 129 | 134 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 276 | 281 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.439 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.396 |
LIG_TYR_ITIM | 217 | 222 | PF00017 | 0.539 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.419 |
LIG_WW_3 | 56 | 60 | PF00397 | 0.385 |
MOD_CDK_SPxxK_3 | 36 | 43 | PF00069 | 0.412 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.684 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.427 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.577 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.423 |
MOD_Cter_Amidation | 241 | 244 | PF01082 | 0.237 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.631 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.639 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.678 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.491 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.342 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.329 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.235 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.434 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.428 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.670 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.500 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.505 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.495 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.371 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.435 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.434 |
MOD_N-GLC_2 | 204 | 206 | PF02516 | 0.179 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.347 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.274 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.438 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.409 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.437 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.438 |
MOD_OFUCOSY | 2 | 7 | PF10250 | 0.403 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.414 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.461 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.396 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.437 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.541 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.635 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.379 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.284 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.379 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.458 |
MOD_SUMO_rev_2 | 134 | 143 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 88 | 97 | PF00179 | 0.297 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.465 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I030 | Leptomonas seymouri | 73% | 100% |
A0A0S4IHR6 | Bodo saltans | 50% | 100% |
A0A1X0NXR2 | Trypanosomatidae | 48% | 100% |
A0A3Q8IDY4 | Leishmania donovani | 79% | 100% |
A0A422NWD3 | Trypanosoma rangeli | 50% | 100% |
D0A1C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AGV9 | Leishmania infantum | 79% | 88% |
E9AV75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QCA6 | Leishmania major | 76% | 100% |
V5B6I0 | Trypanosoma cruzi | 47% | 100% |