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 |
Related structures:
AlphaFold database: A4HQ58
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 3 |
GO:0032259 | methylation | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.223 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.449 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.515 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.391 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.654 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.399 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.302 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.443 |
DOC_MAPK_NFAT4_5 | 300 | 308 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 50 | 57 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.223 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 98 | 101 | PF13499 | 0.425 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.437 |
LIG_14-3-3_CanoR_1 | 241 | 250 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 311 | 320 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.526 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.257 |
LIG_Clathr_ClatBox_1 | 260 | 264 | PF01394 | 0.475 |
LIG_Clathr_ClatBox_1 | 288 | 292 | PF01394 | 0.449 |
LIG_eIF4E_1 | 109 | 115 | PF01652 | 0.311 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.464 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.661 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.438 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.277 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.346 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.461 |
LIG_LIR_Gen_1 | 113 | 124 | PF02991 | 0.324 |
LIG_LIR_LC3C_4 | 257 | 262 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.328 |
LIG_MYND_1 | 97 | 101 | PF01753 | 0.400 |
LIG_PCNA_yPIPBox_3 | 106 | 115 | PF02747 | 0.511 |
LIG_Pex14_2 | 112 | 116 | PF04695 | 0.510 |
LIG_Rb_pABgroove_1 | 52 | 60 | PF01858 | 0.486 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.339 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.444 |
LIG_SUMO_SIM_anti_2 | 257 | 264 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 257 | 264 | PF11976 | 0.475 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.282 |
LIG_WRC_WIRS_1 | 194 | 199 | PF05994 | 0.328 |
LIG_WW_3 | 223 | 227 | PF00397 | 0.223 |
MOD_CDC14_SPxK_1 | 186 | 189 | PF00782 | 0.475 |
MOD_CDK_SPxK_1 | 183 | 189 | PF00069 | 0.475 |
MOD_CDK_SPxxK_3 | 183 | 190 | PF00069 | 0.475 |
MOD_CDK_SPxxK_3 | 199 | 206 | PF00069 | 0.211 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.430 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.172 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.215 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.362 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.428 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.510 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.268 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.423 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.425 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.438 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.364 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.438 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.481 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.556 |
MOD_N-GLC_2 | 179 | 181 | PF02516 | 0.223 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.605 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.389 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.423 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.339 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.518 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.475 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.475 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.437 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.437 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.510 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.344 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.324 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.501 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.455 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.368 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.453 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.427 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.223 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.437 |
MOD_SUMO_rev_2 | 138 | 148 | PF00179 | 0.446 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.223 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.223 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC88 | Leptomonas seymouri | 57% | 99% |
A0A0S4JTC1 | Bodo saltans | 39% | 100% |
A0A1X0P072 | Trypanosomatidae | 41% | 100% |
A0A3S5IRD0 | Trypanosoma rangeli | 44% | 100% |
A0A3S7XBX8 | Leishmania donovani | 81% | 100% |
A4IDV7 | Leishmania infantum | 82% | 100% |
D0A459 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ATX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q0L8 | Leishmania major | 81% | 100% |
V5DLQ3 | Trypanosoma cruzi | 42% | 100% |