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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: E9AJX6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 22 |
GO:0008104 | protein localization | 4 | 22 |
GO:0009987 | cellular process | 1 | 22 |
GO:0015031 | protein transport | 4 | 22 |
GO:0016192 | vesicle-mediated transport | 4 | 22 |
GO:0033036 | macromolecule localization | 2 | 22 |
GO:0045184 | establishment of protein localization | 3 | 22 |
GO:0051179 | localization | 1 | 22 |
GO:0051234 | establishment of localization | 2 | 22 |
GO:0051641 | cellular localization | 2 | 22 |
GO:0070727 | cellular macromolecule localization | 3 | 22 |
GO:0071702 | organic substance transport | 4 | 22 |
GO:0071705 | nitrogen compound transport | 4 | 22 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.516 |
DOC_CYCLIN_RxL_1 | 28 | 39 | PF00134 | 0.582 |
DOC_MAPK_MEF2A_6 | 182 | 189 | PF00069 | 0.695 |
LIG_Actin_WH2_2 | 171 | 188 | PF00022 | 0.518 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.282 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.514 |
LIG_eIF4E_1 | 30 | 36 | PF01652 | 0.580 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.350 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.781 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.681 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.414 |
LIG_GBD_Chelix_1 | 143 | 151 | PF00786 | 0.233 |
LIG_GBD_Chelix_1 | 167 | 175 | PF00786 | 0.260 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 73 | 84 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.353 |
LIG_NRBOX | 83 | 89 | PF00104 | 0.260 |
LIG_PCNA_yPIPBox_3 | 205 | 215 | PF02747 | 0.177 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.641 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.622 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.662 |
LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.683 |
LIG_Sin3_3 | 161 | 168 | PF02671 | 0.210 |
LIG_SUMO_SIM_par_1 | 142 | 149 | PF11976 | 0.203 |
LIG_SxIP_EBH_1 | 171 | 182 | PF03271 | 0.387 |
LIG_UBA3_1 | 147 | 156 | PF00899 | 0.373 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.435 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.684 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.632 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.433 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.387 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.509 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.342 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.622 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.662 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.269 |
MOD_N-GLC_2 | 208 | 210 | PF02516 | 0.210 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.678 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.339 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.357 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.637 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.679 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.677 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.329 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.529 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.631 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.327 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.315 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.410 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.526 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.621 |
MOD_SUMO_rev_2 | 15 | 21 | PF00179 | 0.587 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.617 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5I1 | Leptomonas seymouri | 71% | 98% |
A0A0N1I3M5 | Leptomonas seymouri | 32% | 100% |
A0A1X0P315 | Trypanosomatidae | 33% | 100% |
A0A1X0P7F6 | Trypanosomatidae | 30% | 100% |
A0A1X0P987 | Trypanosomatidae | 44% | 100% |
A0A3Q8IBK0 | Leishmania donovani | 36% | 100% |
A0A3S5H567 | Leishmania donovani | 94% | 99% |
A0A3S5H5K3 | Leishmania donovani | 37% | 100% |
A0A422N175 | Trypanosoma rangeli | 46% | 100% |
A4H3Q4 | Leishmania braziliensis | 87% | 100% |
A4HDV3 | Leishmania braziliensis | 38% | 100% |
A4HRX8 | Leishmania infantum | 94% | 99% |
A4HSK3 | Leishmania infantum | 37% | 100% |
A4I148 | Leishmania infantum | 36% | 100% |
C9ZKI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 78% |
E9ACN7 | Leishmania major | 93% | 100% |
E9AKI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AX82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4QA90 | Leishmania major | 38% | 100% |
Q4QJC1 | Leishmania major | 37% | 100% |