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 |
Related structures:
AlphaFold database: Q4QHA0
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 12 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.624 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.622 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 76 | 82 | PF00069 | 0.512 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.670 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.443 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 187 | 191 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.704 |
LIG_14-3-3_CterR_2 | 356 | 360 | PF00244 | 0.413 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.635 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.599 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.557 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.548 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.585 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.337 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.495 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.685 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.551 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.441 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.770 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.629 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.445 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.611 |
LIG_PTB_Apo_2 | 278 | 285 | PF02174 | 0.557 |
LIG_PTB_Phospho_1 | 278 | 284 | PF10480 | 0.552 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.719 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.719 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.398 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.524 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.685 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.629 |
LIG_SH3_4 | 33 | 40 | PF00018 | 0.563 |
LIG_SUMO_SIM_par_1 | 191 | 196 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 66 | 71 | PF11976 | 0.545 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.581 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.601 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.436 |
LIG_TYR_ITIM | 238 | 243 | PF00017 | 0.430 |
LIG_UBA3_1 | 167 | 172 | PF00899 | 0.624 |
LIG_WW_3 | 223 | 227 | PF00397 | 0.657 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.698 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.621 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.533 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.657 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.800 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.473 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.643 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.551 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.601 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.669 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.684 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.688 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.551 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.634 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.456 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.802 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.750 |
MOD_N-GLC_2 | 334 | 336 | PF02516 | 0.402 |
MOD_N-GLC_2 | 345 | 347 | PF02516 | 0.252 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.637 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.640 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.519 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.674 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.568 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.740 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.749 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.520 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.508 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.708 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.449 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.624 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.557 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.363 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.573 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.419 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.330 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.711 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.643 |
MOD_SUMO_for_1 | 171 | 174 | PF00179 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.554 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A9 | Leptomonas seymouri | 48% | 93% |
A0A0S4ITU9 | Bodo saltans | 30% | 79% |
A0A1X0NRX0 | Trypanosomatidae | 35% | 98% |
A0A3R7KAZ9 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WRB2 | Leishmania donovani | 95% | 100% |
A4H6A2 | Leishmania braziliensis | 79% | 100% |
A4HUM6 | Leishmania infantum | 95% | 100% |
C9ZVQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ANC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BTV5 | Trypanosoma cruzi | 37% | 99% |