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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H458
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008176 | tRNA (guanine-N7-)-methyltransferase activity | 7 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 306 | 310 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.397 |
CLV_PCSK_FUR_1 | 282 | 286 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.326 |
CLV_PCSK_PC7_1 | 197 | 203 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.591 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.623 |
DEG_ODPH_VHL_1 | 103 | 116 | PF01847 | 0.533 |
DOC_CYCLIN_RxL_1 | 124 | 133 | PF00134 | 0.462 |
DOC_CYCLIN_yClb1_LxF_4 | 159 | 164 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 289 | 298 | PF00069 | 0.587 |
DOC_PP1_RVXF_1 | 111 | 118 | PF00149 | 0.488 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.386 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.496 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.497 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.454 |
LIG_APCC_ABBA_1 | 228 | 233 | PF00400 | 0.526 |
LIG_APCC_ABBAyCdc20_2 | 201 | 207 | PF00400 | 0.493 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.371 |
LIG_Clathr_ClatBox_1 | 203 | 207 | PF01394 | 0.487 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.485 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.348 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.419 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.357 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.521 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.396 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.538 |
LIG_LIR_Gen_1 | 136 | 144 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.473 |
LIG_LIR_LC3C_4 | 136 | 140 | PF02991 | 0.438 |
LIG_LIR_LC3C_4 | 247 | 252 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.476 |
LIG_NRBOX | 31 | 37 | PF00104 | 0.565 |
LIG_PTB_Apo_2 | 157 | 164 | PF02174 | 0.270 |
LIG_REV1ctd_RIR_1 | 161 | 170 | PF16727 | 0.464 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.655 |
LIG_SH3_1 | 219 | 225 | PF00018 | 0.483 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.389 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.441 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.337 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.483 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 270 | 278 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 270 | 278 | PF11976 | 0.395 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.340 |
LIG_UBA3_1 | 241 | 249 | PF00899 | 0.487 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.488 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.494 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.498 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.425 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.590 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.477 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.529 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.334 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.439 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.495 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.427 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.467 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.487 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.592 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.523 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.594 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.474 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.428 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.322 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.379 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.300 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.610 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.277 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.300 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.591 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.523 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.501 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.402 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.358 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.396 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.457 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.539 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.535 |
MOD_SUMO_rev_2 | 243 | 251 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 293 | 299 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 309 | 314 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 127 | 132 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 265 | 270 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N8 | Leptomonas seymouri | 67% | 100% |
A0A1X0P3K8 | Trypanosomatidae | 42% | 98% |
A0A3S5H5F9 | Leishmania donovani | 88% | 100% |
A0A3S5ISB0 | Trypanosoma rangeli | 48% | 100% |
A4HSE1 | Leishmania infantum | 88% | 100% |
C9ZPX1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AKB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QJJ1 | Leishmania major | 87% | 100% |
V5AUY0 | Trypanosoma cruzi | 44% | 100% |