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: A4HI64
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008276 | protein methyltransferase activity | 3 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0106370 | protein-L-histidine N-pros-methyltransferase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.253 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.381 |
CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.404 |
CLV_PCSK_PC7_1 | 149 | 155 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.157 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.301 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.157 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.619 |
DEG_SCF_FBW7_1 | 100 | 107 | PF00400 | 0.157 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.336 |
DOC_CYCLIN_RxL_1 | 191 | 204 | PF00134 | 0.157 |
DOC_CYCLIN_RxL_1 | 55 | 66 | PF00134 | 0.281 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 256 | 265 | PF00069 | 0.381 |
DOC_PP2B_LxvP_1 | 98 | 101 | PF13499 | 0.380 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.157 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.181 |
LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 55 | 60 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.284 |
LIG_AP2alpha_2 | 164 | 166 | PF02296 | 0.292 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.292 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.193 |
LIG_DLG_GKlike_1 | 246 | 254 | PF00625 | 0.297 |
LIG_DLG_GKlike_1 | 55 | 62 | PF00625 | 0.336 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.409 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.295 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.145 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.303 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.388 |
LIG_GSK3_LRP6_1 | 104 | 109 | PF00069 | 0.157 |
LIG_Integrin_RGD_1 | 300 | 302 | PF01839 | 0.450 |
LIG_LIR_Gen_1 | 112 | 123 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.215 |
LIG_MLH1_MIPbox_1 | 68 | 72 | PF16413 | 0.157 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.157 |
LIG_PCNA_yPIPBox_3 | 53 | 63 | PF02747 | 0.384 |
LIG_REV1ctd_RIR_1 | 69 | 78 | PF16727 | 0.267 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.253 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.157 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.253 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.238 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.238 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 292 | 298 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.145 |
LIG_TYR_ITIM | 285 | 290 | PF00017 | 0.332 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.157 |
LIG_UBA3_1 | 198 | 207 | PF00899 | 0.332 |
MOD_CDK_SPK_2 | 191 | 196 | PF00069 | 0.157 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.267 |
MOD_DYRK1A_RPxSP_1 | 191 | 195 | PF00069 | 0.157 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.415 |
MOD_GlcNHglycan | 143 | 147 | PF01048 | 0.345 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.352 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.239 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.238 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.397 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.321 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.436 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.296 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.401 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.297 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.335 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.157 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.269 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.381 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.272 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.157 |
MOD_PKB_1 | 53 | 61 | PF00069 | 0.314 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.258 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.487 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.332 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.216 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.256 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.173 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.358 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.391 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.168 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.346 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.298 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.181 |
MOD_SUMO_rev_2 | 5 | 10 | PF00179 | 0.424 |
TRG_DiLeu_BaEn_2 | 45 | 51 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.157 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 196 | 201 | PF00026 | 0.157 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBZ8 | Leptomonas seymouri | 72% | 100% |
A0A0S4J0V6 | Bodo saltans | 46% | 100% |
A0A1X0P223 | Trypanosomatidae | 53% | 92% |
A0A3Q8IJA6 | Leishmania donovani | 84% | 100% |
A0A3S5ISQ6 | Trypanosoma rangeli | 53% | 99% |
A4I5E1 | Leishmania infantum | 83% | 100% |
C9ZQS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 96% |
E9B0N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q0VCJ8 | Bos taurus | 38% | 97% |
Q4Q7J3 | Leishmania major | 83% | 100% |
Q5ZMH6 | Gallus gallus | 36% | 96% |
Q9EPL4 | Mus musculus | 39% | 97% |
Q9H1A3 | Homo sapiens | 38% | 97% |
V5DQR7 | Trypanosoma cruzi | 55% | 98% |