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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034708 | methyltransferase complex | 4 | 1 |
GO:0035657 | eRF1 methyltransferase complex | 5 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HKJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043414 | macromolecule methylation | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.485 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.311 |
DEG_APCC_KENBOX_2 | 274 | 278 | PF00400 | 0.434 |
DOC_CYCLIN_RxL_1 | 68 | 79 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 132 | 142 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 265 | 273 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.474 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 216 | 219 | PF00568 | 0.350 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.569 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 145 | 155 | PF00244 | 0.662 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.640 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.457 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.472 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.495 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.521 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.481 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.645 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.532 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.223 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.679 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.531 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 7 | 12 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 208 | 219 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.367 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.449 |
LIG_PCNA_TLS_4 | 249 | 256 | PF02747 | 0.511 |
LIG_Pex14_1 | 326 | 330 | PF04695 | 0.250 |
LIG_PTB_Apo_2 | 214 | 221 | PF02174 | 0.351 |
LIG_PTB_Phospho_1 | 214 | 220 | PF10480 | 0.347 |
LIG_Rb_LxCxE_1 | 289 | 310 | PF01857 | 0.330 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.537 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.571 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.517 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.607 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.350 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.408 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.638 |
LIG_SUMO_SIM_par_1 | 115 | 120 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.382 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.440 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.483 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.667 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.544 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.449 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.442 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.446 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.529 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.410 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.399 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.448 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.593 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.675 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.700 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.630 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.546 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.350 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.689 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.374 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.682 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.597 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.627 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.295 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.412 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.660 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.396 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.401 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.480 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.617 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.368 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.411 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.475 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.502 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.671 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.545 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.441 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.715 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.410 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.495 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.500 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.481 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.624 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.440 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.382 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.461 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.316 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.433 |
MOD_SUMO_for_1 | 302 | 305 | PF00179 | 0.581 |
MOD_SUMO_for_1 | 89 | 92 | PF00179 | 0.743 |
TRG_DiLeu_BaEn_2 | 30 | 36 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A8 | Leptomonas seymouri | 56% | 94% |
A0A0S4JAA0 | Bodo saltans | 38% | 100% |
A0A1X0NUU4 | Trypanosomatidae | 41% | 100% |
A0A3Q8IFZ7 | Leishmania donovani | 81% | 100% |
A0A3R7LIX6 | Trypanosoma rangeli | 43% | 100% |
A4I831 | Leishmania infantum | 82% | 100% |
D0AA96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B2Y9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q567 | Leishmania major | 80% | 100% |
V5BBL2 | Trypanosoma cruzi | 43% | 100% |