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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9ALS5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.668 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.507 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.622 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.624 |
DOC_MAPK_gen_1 | 203 | 211 | PF00069 | 0.709 |
DOC_MAPK_MEF2A_6 | 122 | 131 | PF00069 | 0.712 |
DOC_PP1_RVXF_1 | 22 | 28 | PF00149 | 0.552 |
DOC_PP2B_LxvP_1 | 141 | 144 | PF13499 | 0.707 |
DOC_PP2B_PxIxI_1 | 126 | 132 | PF00149 | 0.707 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.668 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 101 | 110 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 122 | 129 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.669 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.653 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.677 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.679 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.532 |
LIG_LIR_Apic_2 | 78 | 82 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.669 |
LIG_Pex14_1 | 237 | 241 | PF04695 | 0.545 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.552 |
LIG_SH2_CRK | 2 | 6 | PF00017 | 0.645 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.617 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.593 |
LIG_SH2_SRC | 243 | 246 | PF00017 | 0.229 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.566 |
LIG_SH3_1 | 272 | 278 | PF00018 | 0.469 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.477 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.630 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.680 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.708 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.691 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.662 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.529 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.672 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.533 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.483 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.481 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.461 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.814 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.727 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.661 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.633 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.560 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.668 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.801 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.429 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.701 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.661 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.508 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.615 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.635 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.640 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.569 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.684 |
MOD_PK_1 | 42 | 48 | PF00069 | 0.643 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.673 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.631 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.713 |
MOD_PKB_1 | 111 | 119 | PF00069 | 0.632 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.673 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.626 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.768 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.474 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 158 | 163 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.646 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7L3 | Leishmania donovani | 75% | 100% |
A4HHG0 | Leishmania braziliensis | 59% | 81% |
A4I4L0 | Leishmania infantum | 76% | 100% |
E9AE07 | Leishmania major | 81% | 100% |