Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QDS7
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_NRD_NRD_1 | 173 | 175 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.623 |
DOC_ANK_TNKS_1 | 48 | 55 | PF00023 | 0.564 |
DOC_MAPK_gen_1 | 174 | 182 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 174 | 182 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 198 | 205 | PF00069 | 0.396 |
DOC_MAPK_NFAT4_5 | 175 | 183 | PF00069 | 0.552 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.441 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.507 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 339 | 349 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.567 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.411 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.374 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.469 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.531 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.560 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.339 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.693 |
LIG_MYND_1 | 158 | 162 | PF01753 | 0.583 |
LIG_PDZ_Class_1 | 355 | 360 | PF00595 | 0.639 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.717 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.561 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 196 | 199 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.450 |
LIG_SH3_1 | 330 | 336 | PF00018 | 0.300 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.422 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.286 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.724 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.516 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.526 |
LIG_WRC_WIRS_1 | 122 | 127 | PF05994 | 0.440 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.493 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.609 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.698 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.529 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.688 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.670 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.637 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.757 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.424 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.419 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.401 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.523 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.382 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.792 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.851 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.445 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.647 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.753 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.742 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.773 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.837 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.386 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.554 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.608 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.529 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.391 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.714 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.550 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.432 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.424 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.469 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.368 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.556 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.547 |
MOD_Plk_2-3 | 236 | 242 | PF00069 | 0.428 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.535 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.496 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.321 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.688 |
MOD_SUMO_for_1 | 158 | 161 | PF00179 | 0.481 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.466 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.436 |
TRG_NLS_MonoExtN_4 | 245 | 251 | PF00514 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMI8 | Leptomonas seymouri | 73% | 98% |
A0A0S4JNW6 | Bodo saltans | 36% | 94% |
A0A1X0P805 | Trypanosomatidae | 59% | 97% |
A0A3S7WV37 | Leishmania donovani | 93% | 99% |
A0A422P0Q0 | Trypanosoma rangeli | 54% | 100% |
A4H9M5 | Leishmania braziliensis | 80% | 100% |
A4HXY9 | Leishmania infantum | 93% | 98% |
D0A5B8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ARQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BNN3 | Trypanosoma cruzi | 54% | 100% |