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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q849
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 4 |
GO:0032259 | methylation | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0008168 | methyltransferase activity | 4 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.394 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 184 | 186 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.393 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.412 |
DOC_CYCLIN_RxL_1 | 181 | 191 | PF00134 | 0.358 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 184 | 195 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.618 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.297 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.412 |
LIG_14-3-3_CanoR_1 | 171 | 175 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.579 |
LIG_APCC_ABBA_1 | 13 | 18 | PF00400 | 0.406 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.276 |
LIG_CaM_IQ_9 | 163 | 179 | PF13499 | 0.425 |
LIG_Clathr_ClatBox_1 | 105 | 109 | PF01394 | 0.297 |
LIG_eIF4E_1 | 226 | 232 | PF01652 | 0.397 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.417 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.449 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.550 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.450 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.448 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.403 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.291 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.337 |
LIG_Pex14_2 | 129 | 133 | PF04695 | 0.276 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.312 |
LIG_SH2_NCK_1 | 83 | 87 | PF00017 | 0.253 |
LIG_SH2_PTP2 | 178 | 181 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.273 |
LIG_SH2_STAT3 | 226 | 229 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.300 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 212 | 217 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 11 | 18 | PF11976 | 0.517 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.546 |
MOD_CDK_SPxxK_3 | 177 | 184 | PF00069 | 0.418 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.555 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.296 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.425 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.479 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.406 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.355 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.319 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.316 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.380 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.333 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.468 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.344 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.389 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.541 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.439 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.300 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.476 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.346 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.245 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.473 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.413 |
TRG_DiLeu_BaEn_2 | 169 | 175 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 182 | 187 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.478 |
TRG_NES_CRM1_1 | 125 | 139 | PF08389 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 24 | 29 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P1 | Leptomonas seymouri | 74% | 100% |
A0A0S4IRT5 | Bodo saltans | 47% | 98% |
A0A1X0NQR6 | Trypanosomatidae | 50% | 100% |
A0A3Q8IGV9 | Leishmania donovani | 96% | 100% |
A0A422N7I7 | Trypanosoma rangeli | 39% | 100% |
A4HGS0 | Leishmania braziliensis | 88% | 100% |
A4I3U5 | Leishmania infantum | 96% | 100% |
E9B037 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |