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: E9ANC4
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_NRD_NRD_1 | 76 | 78 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.358 |
DOC_CYCLIN_RxL_1 | 91 | 102 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 76 | 82 | PF00069 | 0.500 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.414 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.543 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.457 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 187 | 191 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.302 |
LIG_14-3-3_CterR_2 | 356 | 360 | PF00244 | 0.347 |
LIG_Actin_WH2_2 | 119 | 135 | PF00022 | 0.347 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.569 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.474 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.501 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.528 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.637 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.505 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.273 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.461 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.580 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.387 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.625 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.469 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.453 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.363 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.489 |
LIG_PTB_Apo_2 | 278 | 285 | PF02174 | 0.509 |
LIG_PTB_Phospho_1 | 278 | 284 | PF10480 | 0.508 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.384 |
LIG_SH3_1 | 226 | 232 | PF00018 | 0.519 |
LIG_SH3_2 | 229 | 234 | PF14604 | 0.476 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.474 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.755 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.557 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.622 |
LIG_SUMO_SIM_par_1 | 191 | 196 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 66 | 71 | PF11976 | 0.472 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.543 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.595 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.497 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.375 |
LIG_TYR_ITIM | 238 | 243 | PF00017 | 0.369 |
LIG_UBA3_1 | 167 | 172 | PF00899 | 0.583 |
MOD_CDK_SPK_2 | 247 | 252 | PF00069 | 0.403 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.604 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.487 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.598 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.624 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.473 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.528 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.611 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.515 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.607 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.629 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.686 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.424 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.669 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.733 |
MOD_N-GLC_2 | 334 | 336 | PF02516 | 0.352 |
MOD_N-GLC_2 | 345 | 347 | PF02516 | 0.212 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.586 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.622 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.445 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.331 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.622 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.507 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.704 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.772 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.450 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.469 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.406 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.316 |
MOD_Plk_2-3 | 300 | 306 | PF00069 | 0.554 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.548 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.374 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.275 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.698 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.480 |
MOD_SUMO_for_1 | 171 | 174 | PF00179 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6A9 | Leptomonas seymouri | 47% | 93% |
A0A1X0NRX0 | Trypanosomatidae | 36% | 98% |
A0A3R7KAZ9 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WRB2 | Leishmania donovani | 94% | 100% |
A4H6A2 | Leishmania braziliensis | 79% | 99% |
A4HUM6 | Leishmania infantum | 94% | 100% |
C9ZVQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QHA0 | Leishmania major | 93% | 100% |
V5BTV5 | Trypanosoma cruzi | 37% | 99% |