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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9ARC1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.383 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.495 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.204 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.531 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.204 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.750 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.246 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 48 | 52 | PF00244 | 0.189 |
LIG_Clathr_ClatBox_1 | 57 | 61 | PF01394 | 0.324 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.586 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.552 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.653 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.633 |
LIG_LIR_Gen_1 | 61 | 71 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.452 |
LIG_SH2_NCK_1 | 76 | 80 | PF00017 | 0.390 |
LIG_SH2_SRC | 76 | 79 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.449 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.707 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.779 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.806 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.568 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.541 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.349 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.776 |
MOD_CDK_SPK_2 | 144 | 149 | PF00069 | 0.595 |
MOD_CDK_SPxxK_3 | 122 | 129 | PF00069 | 0.749 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.758 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.555 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.624 |
MOD_DYRK1A_RPxSP_1 | 48 | 52 | PF00069 | 0.204 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.596 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.483 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.531 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.809 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.529 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.537 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.745 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.663 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.614 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.674 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.604 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.204 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.650 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.593 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.325 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.640 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.668 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.748 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.705 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.780 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.563 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.706 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.246 |
MOD_SUMO_rev_2 | 250 | 258 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.641 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.718 |
TRG_DiLeu_BaEn_4 | 272 | 278 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.507 |
TRG_NES_CRM1_1 | 224 | 236 | PF08389 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HR49 | Leptomonas seymouri | 41% | 100% |
A0A3Q8IE41 | Leishmania donovani | 78% | 100% |
A4H9A5 | Leishmania braziliensis | 63% | 100% |
A4HTR3 | Leishmania infantum | 79% | 100% |
A4HXM5 | Leishmania infantum | 78% | 100% |
C9ZUK7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4QBZ4 | Leishmania major | 78% | 100% |
Q4QE42 | Leishmania major | 79% | 100% |