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: E9AYQ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0016485 | protein processing | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0051604 | protein maturation | 4 | 11 |
GO:0071586 | CAAX-box protein processing | 6 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004222 | metalloendopeptidase activity | 5 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.513 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.296 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.648 |
DOC_PP1_RVXF_1 | 77 | 84 | PF00149 | 0.384 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.419 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.303 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.325 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.334 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.651 |
LIG_LIR_Apic_2 | 53 | 57 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 6 | 17 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.299 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.447 |
LIG_NRBOX | 81 | 87 | PF00104 | 0.313 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.418 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.463 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.391 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.671 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.364 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.357 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.391 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.441 |
MOD_CDC14_SPxK_1 | 91 | 94 | PF00782 | 0.237 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.212 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.466 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.660 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.370 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.210 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.371 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.450 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.424 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.595 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.608 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.511 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.345 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.351 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.430 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.666 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.347 |
MOD_PKB_1 | 194 | 202 | PF00069 | 0.582 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.587 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.343 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.624 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.302 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.463 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.303 |
MOD_SUMO_rev_2 | 116 | 126 | PF00179 | 0.597 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.252 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.691 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.600 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS3 | Leptomonas seymouri | 46% | 79% |
A0A0S4JSY4 | Bodo saltans | 33% | 72% |
A0A1X0NYX6 | Trypanosomatidae | 35% | 74% |
A0A3S7X0B2 | Leishmania donovani | 87% | 100% |
A4HFB3 | Leishmania braziliensis | 72% | 100% |
A4I2J5 | Leishmania infantum | 87% | 100% |
C9ZK27 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 74% |
Q4Q8S2 | Leishmania major | 88% | 100% |
V5BHT4 | Trypanosoma cruzi | 32% | 93% |