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:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9AM95
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.539 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.704 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.379 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.694 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.617 |
DOC_CDC14_PxL_1 | 198 | 206 | PF14671 | 0.417 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 104 | 114 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.668 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.282 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.764 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.499 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.572 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.352 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.443 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.769 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.492 |
LIG_LYPXL_S_1 | 186 | 190 | PF13949 | 0.656 |
LIG_LYPXL_yS_3 | 187 | 190 | PF13949 | 0.426 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.398 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.406 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.392 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.446 |
LIG_SUMO_SIM_par_1 | 16 | 21 | PF11976 | 0.729 |
LIG_SxIP_EBH_1 | 36 | 49 | PF03271 | 0.644 |
LIG_TYR_ITIM | 177 | 182 | PF00017 | 0.440 |
LIG_TYR_ITSM | 115 | 122 | PF00017 | 0.420 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.399 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.738 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.727 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.775 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.774 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.397 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.669 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.570 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.550 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.512 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.396 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.505 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.540 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.722 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.703 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.714 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.678 |
MOD_N-GLC_2 | 183 | 185 | PF02516 | 0.621 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.465 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.387 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.700 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.492 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.706 |
MOD_PK_1 | 39 | 45 | PF00069 | 0.582 |
MOD_PK_1 | 60 | 66 | PF00069 | 0.593 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.483 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.424 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.747 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.714 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.413 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.354 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.376 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.433 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.376 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.739 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.739 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAL2 | Leptomonas seymouri | 48% | 100% |
A0A0S4IYT0 | Bodo saltans | 32% | 100% |
A0A1X0NNX7 | Trypanosomatidae | 36% | 88% |
A0A3S7WQ61 | Leishmania donovani | 88% | 100% |
A4H583 | Leishmania braziliensis | 74% | 100% |
A4HTG7 | Leishmania infantum | 88% | 100% |
Q4QIF3 | Leishmania major | 89% | 100% |