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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B4B7
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: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:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 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: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:0051603 | proteolysis involved in protein catabolic process | 5 | 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:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016874 | ligase activity | 2 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 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 | 139 | 141 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.669 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.264 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.298 |
DEG_SCF_TRCP1_1 | 184 | 190 | PF00400 | 0.529 |
DOC_CYCLIN_RxL_1 | 105 | 116 | PF00134 | 0.264 |
DOC_CYCLIN_RxL_1 | 207 | 216 | PF00134 | 0.612 |
DOC_MAPK_MEF2A_6 | 53 | 60 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.278 |
DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.587 |
DOC_SPAK_OSR1_1 | 53 | 57 | PF12202 | 0.358 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.264 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.293 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 29 | 37 | PF00244 | 0.159 |
LIG_Actin_RPEL_3 | 88 | 107 | PF02755 | 0.358 |
LIG_APCC_ABBA_1 | 57 | 62 | PF00400 | 0.233 |
LIG_EVH1_2 | 68 | 72 | PF00568 | 0.358 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.779 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.318 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.649 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.667 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.658 |
LIG_Integrin_RGD_1 | 85 | 87 | PF01839 | 0.358 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.278 |
LIG_LYPXL_yS_3 | 64 | 67 | PF13949 | 0.264 |
LIG_REV1ctd_RIR_1 | 70 | 79 | PF16727 | 0.358 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 145 | 149 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.586 |
LIG_SH3_2 | 65 | 70 | PF14604 | 0.264 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.264 |
LIG_SUMO_SIM_par_1 | 55 | 62 | PF11976 | 0.321 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.537 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.704 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.745 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.577 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.644 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.661 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.653 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.452 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.264 |
MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.702 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.635 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.630 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.556 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.553 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.602 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.589 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.626 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.660 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.332 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.595 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.315 |
MOD_PKA_1 | 210 | 216 | PF00069 | 0.557 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.619 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.324 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.463 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.478 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.264 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.293 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 133 | 143 | PF00179 | 0.358 |
TRG_DiLeu_BaEn_1 | 126 | 131 | PF01217 | 0.264 |
TRG_DiLeu_LyEn_5 | 126 | 131 | PF01217 | 0.264 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.264 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.667 |
TRG_NLS_MonoExtN_4 | 232 | 238 | PF00514 | 0.699 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.280 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 9 | 14 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P683 | Leptomonas seymouri | 72% | 100% |
A0A1X0NPI5 | Trypanosomatidae | 33% | 100% |
A0A1X0NSR5 | Trypanosomatidae | 59% | 86% |
A0A3Q8IFB8 | Leishmania donovani | 29% | 100% |
A0A3Q8IMQ9 | Leishmania donovani | 92% | 100% |
A0A3S5H604 | Leishmania donovani | 43% | 100% |
A4H533 | Leishmania braziliensis | 40% | 100% |
A4H861 | Leishmania braziliensis | 81% | 100% |
A4HTB1 | Leishmania infantum | 43% | 100% |
A4I7L2 | Leishmania infantum | 29% | 100% |
A4I9B7 | Leishmania infantum | 92% | 100% |
B5DFI8 | Rattus norvegicus | 42% | 100% |
E9ALA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B2J3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
P49427 | Homo sapiens | 31% | 100% |
P61085 | Bos taurus | 27% | 100% |
P61086 | Homo sapiens | 27% | 100% |
P61087 | Mus musculus | 27% | 100% |
Q08BH7 | Danio rerio | 31% | 100% |
Q1RML1 | Bos taurus | 37% | 100% |
Q4Q3Q8 | Leishmania major | 89% | 100% |
Q4Q5L3 | Leishmania major | 29% | 100% |
Q4QIK2 | Leishmania major | 40% | 100% |
Q7ZY08 | Xenopus laevis | 32% | 100% |
Q8AVU2 | Xenopus laevis | 37% | 100% |
Q8CFI2 | Mus musculus | 31% | 100% |
Q9FF66 | Arabidopsis thaliana | 44% | 96% |
V5BAJ3 | Trypanosoma cruzi | 48% | 100% |