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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AW10
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 | 26 | 28 | PF00675 | 0.479 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.572 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.530 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.447 |
DOC_CYCLIN_RxL_1 | 24 | 33 | PF00134 | 0.313 |
DOC_MAPK_MEF2A_6 | 35 | 43 | PF00069 | 0.503 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.527 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.533 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.350 |
LIG_AP2alpha_2 | 247 | 249 | PF02296 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.469 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.314 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.406 |
LIG_Clathr_ClatBox_1 | 29 | 33 | PF01394 | 0.485 |
LIG_CtBP_PxDLS_1 | 135 | 139 | PF00389 | 0.432 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.258 |
LIG_HCF-1_HBM_1 | 17 | 20 | PF13415 | 0.469 |
LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 33 | 43 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.269 |
LIG_NRBOX | 70 | 76 | PF00104 | 0.492 |
LIG_Pex14_1 | 85 | 89 | PF04695 | 0.369 |
LIG_SH2_GRB2like | 20 | 23 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 83 | 86 | PF00017 | 0.406 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.361 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.515 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.492 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 137 | 144 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 154 | 159 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 70 | 79 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 28 | 33 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 70 | 79 | PF11976 | 0.282 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.466 |
LIG_WRC_WIRS_1 | 175 | 180 | PF05994 | 0.406 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.524 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.350 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.609 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.210 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.602 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.510 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.549 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.378 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.607 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.298 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.432 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.359 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.363 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.442 |
MOD_PKB_1 | 55 | 63 | PF00069 | 0.542 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.365 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.335 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.444 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.406 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.523 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.523 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.263 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.454 |
TRG_NES_CRM1_1 | 223 | 236 | PF08389 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I266 | Leptomonas seymouri | 55% | 100% |
A0A0S4J1S6 | Bodo saltans | 40% | 84% |
A0A1X0NX63 | Trypanosomatidae | 44% | 100% |
A0A3S7WXK7 | Leishmania donovani | 93% | 100% |
A4HCM3 | Leishmania braziliensis | 79% | 100% |
A4I047 | Leishmania infantum | 92% | 100% |
Q4QBG6 | Leishmania major | 92% | 100% |