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: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: E9AJZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.451 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.330 |
DOC_CYCLIN_RxL_1 | 58 | 67 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 186 | 194 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.355 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.454 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.418 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.349 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.462 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.439 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.469 |
LIG_LIR_Apic_2 | 195 | 199 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.368 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.389 |
LIG_Pex14_1 | 196 | 200 | PF04695 | 0.371 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.497 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.339 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.403 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 101 | 105 | PF00017 | 0.193 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 47 | 50 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.376 |
LIG_SH3_1 | 112 | 118 | PF00018 | 0.368 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.486 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.498 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.426 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.365 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.381 |
LIG_TYR_ITSM | 97 | 104 | PF00017 | 0.476 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.431 |
MOD_GlcNHglycan | 100 | 104 | PF01048 | 0.462 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.469 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.371 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.391 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.502 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.472 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.427 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.371 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.429 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.473 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.419 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.333 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.441 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.180 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 75 | 85 | PF00179 | 0.519 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTY0 | Leptomonas seymouri | 67% | 99% |
A0A0S4IH71 | Bodo saltans | 40% | 92% |
A0A0S4IJP7 | Bodo saltans | 28% | 100% |
A0A0S4J8X8 | Bodo saltans | 40% | 100% |
A0A1X0NMV1 | Trypanosomatidae | 49% | 100% |
A0A3S5H574 | Leishmania donovani | 89% | 100% |
A0A422NN81 | Trypanosoma rangeli | 44% | 100% |
A4H3S8 | Leishmania braziliensis | 85% | 100% |
A4HS03 | Leishmania infantum | 88% | 100% |
C9ZY01 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
P0DPD7 | Homo sapiens | 30% | 96% |
Q95Z88 | Leishmania major | 91% | 100% |
V5BI94 | Trypanosoma cruzi | 48% | 100% |