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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B4R1
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 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 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016874 | ligase activity | 2 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 1 |
GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.322 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.421 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.528 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.528 |
DOC_MAPK_gen_1 | 10 | 16 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.528 |
DOC_MAPK_HePTP_8 | 269 | 281 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 81 | 90 | PF00069 | 0.528 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.528 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 98 | 104 | PF00928 | 0.528 |
LIG_DLG_GKlike_1 | 273 | 280 | PF00625 | 0.392 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.528 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.539 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.649 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.528 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.711 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.826 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.528 |
LIG_LIR_Apic_2 | 65 | 71 | PF02991 | 0.528 |
LIG_PCNA_PIPBox_1 | 34 | 43 | PF02747 | 0.528 |
LIG_PCNA_yPIPBox_3 | 28 | 41 | PF02747 | 0.513 |
LIG_PTB_Apo_2 | 89 | 96 | PF02174 | 0.528 |
LIG_PTB_Phospho_1 | 89 | 95 | PF10480 | 0.528 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.649 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.528 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.699 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 276 | 282 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 108 | 115 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.528 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.488 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.706 |
LIG_WRC_WIRS_1 | 113 | 118 | PF05994 | 0.528 |
MOD_CDK_SPK_2 | 171 | 176 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 74 | 81 | PF00069 | 0.528 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.750 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.776 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.528 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.551 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.733 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.687 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.826 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.547 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.397 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.541 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.328 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.586 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.480 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.705 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.823 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.811 |
MOD_LATS_1 | 254 | 260 | PF00433 | 0.664 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.453 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.328 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.271 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.546 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.528 |
MOD_PK_1 | 69 | 75 | PF00069 | 0.528 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.528 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.734 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.528 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.423 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.696 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.775 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.599 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.575 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.539 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.672 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.590 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.655 |
TRG_NLS_MonoCore_2 | 243 | 248 | PF00514 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 17 | 22 | PF00026 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHC0 | Leishmania donovani | 93% | 100% |
A0A3Q8IMQ9 | Leishmania donovani | 26% | 100% |
A4HAK3 | Leishmania braziliensis | 80% | 99% |
A4HAK5 | Leishmania braziliensis | 80% | 99% |
A4HAK6 | Leishmania braziliensis | 81% | 99% |
A4I9B7 | Leishmania infantum | 26% | 100% |
A4I9P7 | Leishmania infantum | 93% | 100% |
C9ZU73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 82% |
Q4Q3B5 | Leishmania major | 93% | 99% |
Q4Q3Q8 | Leishmania major | 28% | 100% |
Q74Z34 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 35% | 100% |
Q9FK29 | Arabidopsis thaliana | 34% | 100% |