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 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AGL4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.556 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.585 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.279 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.547 |
DOC_MAPK_DCC_7 | 98 | 106 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 155 | 162 | PF00149 | 0.314 |
DOC_PP4_FxxP_1 | 16 | 19 | PF00568 | 0.538 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.309 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.537 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.286 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.370 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.430 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.544 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.567 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.314 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.265 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.594 |
LIG_LIR_Apic_2 | 13 | 19 | PF02991 | 0.503 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.306 |
LIG_LIR_Apic_2 | 193 | 199 | PF02991 | 0.749 |
LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.518 |
LIG_LIR_Apic_2 | 20 | 24 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 64 | 72 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.597 |
LIG_LIR_LC3C_4 | 129 | 132 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.555 |
LIG_PCNA_PIPBox_1 | 152 | 161 | PF02747 | 0.336 |
LIG_PCNA_yPIPBox_3 | 152 | 166 | PF02747 | 0.291 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.564 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.374 |
LIG_PTB_Apo_2 | 144 | 151 | PF02174 | 0.309 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.374 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.644 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.530 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.593 |
LIG_Sin3_3 | 49 | 56 | PF02671 | 0.226 |
LIG_SUMO_SIM_par_1 | 128 | 134 | PF11976 | 0.408 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.374 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.337 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.554 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.693 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.343 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.612 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.368 |
MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.526 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.656 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.314 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.330 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.448 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.530 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.354 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.546 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.306 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.427 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.344 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.341 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.358 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.572 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.511 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.516 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.520 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.615 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.514 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.269 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.352 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.479 |
MOD_Plk_2-3 | 40 | 46 | PF00069 | 0.330 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.550 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.326 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.357 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.579 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.534 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.533 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.374 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I195 | Leptomonas seymouri | 64% | 100% |
A0A0S4IKP2 | Bodo saltans | 30% | 96% |
A0A0S4JKJ4 | Bodo saltans | 25% | 90% |
A0A3Q8I8V9 | Leishmania donovani | 100% | 100% |
A4H7Q8 | Leishmania braziliensis | 79% | 100% |
E9ACR4 | Leishmania major | 93% | 100% |
E9APV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |