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: Q4Q0L8
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_NRD_NRD_1 | 106 | 108 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.392 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.438 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.313 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.590 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.345 |
DOC_CYCLIN_RxL_1 | 94 | 104 | PF00134 | 0.419 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.391 |
DOC_MAPK_NFAT4_5 | 301 | 309 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 50 | 57 | PF00149 | 0.301 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.332 |
DOC_PP4_MxPP_1 | 201 | 204 | PF00568 | 0.319 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.247 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.457 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.299 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 312 | 321 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 69 | 73 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 25 | 41 | PF00022 | 0.348 |
LIG_APCC_ABBA_1 | 356 | 361 | PF00400 | 0.154 |
LIG_BIR_III_4 | 317 | 321 | PF00653 | 0.178 |
LIG_Clathr_ClatBox_1 | 261 | 265 | PF01394 | 0.323 |
LIG_Clathr_ClatBox_1 | 289 | 293 | PF01394 | 0.391 |
LIG_eIF4E_1 | 83 | 89 | PF01652 | 0.251 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.639 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.438 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.461 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.282 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.380 |
LIG_LIR_LC3C_4 | 258 | 263 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.154 |
LIG_PCNA_yPIPBox_3 | 107 | 116 | PF02747 | 0.452 |
LIG_Pex14_2 | 113 | 117 | PF04695 | 0.358 |
LIG_Rb_pABgroove_1 | 52 | 60 | PF01858 | 0.346 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.178 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 83 | 86 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.227 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.359 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.203 |
LIG_SUMO_SIM_anti_2 | 258 | 265 | PF11976 | 0.307 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 302 | 308 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 258 | 265 | PF11976 | 0.323 |
LIG_WRC_WIRS_1 | 195 | 200 | PF05994 | 0.247 |
MOD_CDC14_SPxK_1 | 187 | 190 | PF00782 | 0.323 |
MOD_CDC14_SPxK_1 | 224 | 227 | PF00782 | 0.251 |
MOD_CDK_SPK_2 | 184 | 189 | PF00069 | 0.275 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.323 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.251 |
MOD_CDK_SPxxK_3 | 184 | 191 | PF00069 | 0.323 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.263 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.378 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.354 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.366 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.373 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.356 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.311 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.301 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.328 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.370 |
MOD_GlcNHglycan | 317 | 321 | PF01048 | 0.394 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.463 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.367 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.463 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.295 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.251 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.502 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.546 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.303 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.260 |
MOD_NEK2_2 | 237 | 242 | PF00069 | 0.323 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.323 |
MOD_PK_1 | 253 | 259 | PF00069 | 0.275 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.299 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.299 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.356 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.300 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.308 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.457 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.323 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.382 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.360 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.299 |
MOD_SUMO_rev_2 | 139 | 149 | PF00179 | 0.386 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.371 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.449 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.392 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.275 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC88 | Leptomonas seymouri | 58% | 99% |
A0A0S4JTC1 | Bodo saltans | 38% | 100% |
A0A1X0P072 | Trypanosomatidae | 41% | 100% |
A0A3S5IRD0 | Trypanosoma rangeli | 43% | 100% |
A0A3S7XBX8 | Leishmania donovani | 94% | 100% |
A4HQ58 | Leishmania braziliensis | 81% | 100% |
A4IDV7 | Leishmania infantum | 94% | 100% |
D0A459 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ATX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q9AJU0 | Streptomyces olivaceus | 27% | 100% |
V5DLQ3 | Trypanosoma cruzi | 41% | 100% |