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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H6A2
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 11 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.466 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.377 |
DEG_SCF_FBW7_1 | 176 | 183 | PF00400 | 0.424 |
DOC_CYCLIN_RxL_1 | 94 | 102 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.544 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.520 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.385 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.623 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.379 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.591 |
LIG_14-3-3_CterR_2 | 351 | 355 | PF00244 | 0.365 |
LIG_Actin_WH2_2 | 119 | 135 | PF00022 | 0.346 |
LIG_BIR_III_4 | 295 | 299 | PF00653 | 0.465 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.638 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.477 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.539 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.528 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.652 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.505 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.273 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.454 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.581 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.519 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.586 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.367 |
LIG_GBD_Chelix_1 | 14 | 22 | PF00786 | 0.429 |
LIG_GSK3_LRP6_1 | 86 | 91 | PF00069 | 0.521 |
LIG_HP1_1 | 161 | 165 | PF01393 | 0.314 |
LIG_Integrin_RGD_1 | 289 | 291 | PF01839 | 0.434 |
LIG_NRBOX | 163 | 169 | PF00104 | 0.312 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.444 |
LIG_PTB_Apo_2 | 273 | 280 | PF02174 | 0.508 |
LIG_PTB_Phospho_1 | 273 | 279 | PF10480 | 0.503 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.272 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.452 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.429 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.481 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.692 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.384 |
LIG_SH3_4 | 226 | 233 | PF00018 | 0.343 |
LIG_SUMO_SIM_par_1 | 191 | 196 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 66 | 71 | PF11976 | 0.470 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.571 |
LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.371 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.364 |
LIG_TYR_ITIM | 233 | 238 | PF00017 | 0.354 |
LIG_UBA3_1 | 164 | 172 | PF00899 | 0.535 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.477 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.592 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.561 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.455 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.595 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.641 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.603 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.407 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.416 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.658 |
MOD_N-GLC_2 | 329 | 331 | PF02516 | 0.352 |
MOD_N-GLC_2 | 340 | 342 | PF02516 | 0.212 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.575 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.552 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.195 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.247 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.450 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.334 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.612 |
MOD_OFUCOSY | 326 | 331 | PF10250 | 0.195 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.509 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.699 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.547 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.463 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.406 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.316 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.470 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.567 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.356 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.275 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.529 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.628 |
MOD_SUMO_for_1 | 171 | 174 | PF00179 | 0.568 |
TRG_DiLeu_BaEn_4 | 242 | 248 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.551 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.562 |
TRG_NLS_MonoExtN_4 | 226 | 232 | PF00514 | 0.354 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A9 | Leptomonas seymouri | 49% | 91% |
A0A1X0NRX0 | Trypanosomatidae | 36% | 97% |
A0A3R7KAZ9 | Trypanosoma rangeli | 34% | 98% |
A0A3S7WRB2 | Leishmania donovani | 79% | 99% |
A4HUM6 | Leishmania infantum | 78% | 99% |
C9ZVQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ANC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q4QHA0 | Leishmania major | 79% | 100% |
V5BTV5 | Trypanosoma cruzi | 35% | 98% |