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: A0A3Q8IFZ7
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 | 0.536 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.490 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 46 | 50 | PF03568 | 0.423 |
DEG_APCC_KENBOX_2 | 274 | 278 | PF00400 | 0.418 |
DOC_CYCLIN_RxL_1 | 68 | 77 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 155 | 161 | PF00134 | 0.673 |
DOC_MAPK_gen_1 | 265 | 273 | PF00069 | 0.468 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.672 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.501 |
DOC_PP4_FxxP_1 | 216 | 219 | PF00568 | 0.331 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.575 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.423 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 145 | 155 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 34 | 51 | PF00022 | 0.428 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.621 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.476 |
LIG_CtBP_PxDLS_1 | 168 | 172 | PF00389 | 0.524 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.499 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.489 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.589 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.437 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.695 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.677 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.528 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.379 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.434 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.610 |
LIG_LIR_Apic_2 | 8 | 12 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 208 | 219 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.342 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.434 |
LIG_PCNA_TLS_4 | 249 | 256 | PF02747 | 0.481 |
LIG_PTB_Apo_2 | 214 | 221 | PF02174 | 0.333 |
LIG_PTB_Phospho_1 | 214 | 220 | PF10480 | 0.329 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.392 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.609 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.747 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.343 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.382 |
LIG_SUMO_SIM_par_1 | 115 | 120 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 157 | 162 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.367 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.419 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.699 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.457 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.611 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.443 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.347 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.517 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.496 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.380 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.453 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.567 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.565 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.666 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.692 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.651 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.635 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.644 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.326 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.689 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.356 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.614 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.674 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.651 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.403 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.525 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.675 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.522 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.400 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.599 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.586 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.424 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.570 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.458 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.405 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.501 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.670 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.572 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.453 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.627 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.431 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.460 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.641 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.415 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.486 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.521 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.436 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.357 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.451 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.292 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.417 |
MOD_SUMO_for_1 | 302 | 305 | PF00179 | 0.620 |
TRG_DiLeu_BaEn_2 | 30 | 36 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A8 | Leptomonas seymouri | 57% | 94% |
A0A0S4JAA0 | Bodo saltans | 37% | 100% |
A0A1X0NUU4 | Trypanosomatidae | 41% | 100% |
A0A3R7LIX6 | Trypanosoma rangeli | 42% | 100% |
A4HKJ9 | Leishmania braziliensis | 81% | 100% |
A4I831 | Leishmania infantum | 100% | 100% |
D0AA96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B2Y9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q567 | Leishmania major | 91% | 100% |
V5BBL2 | Trypanosoma cruzi | 41% | 100% |