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 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AL05
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.425 |
DOC_MAPK_DCC_7 | 125 | 134 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 125 | 134 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 199 | 208 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 53 | 62 | PF00069 | 0.516 |
DOC_MAPK_NFAT4_5 | 199 | 207 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.720 |
DOC_PP2B_PxIxI_1 | 55 | 61 | PF00149 | 0.369 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.673 |
DOC_USP7_MATH_2 | 96 | 102 | PF00917 | 0.536 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.726 |
LIG_Actin_WH2_2 | 146 | 161 | PF00022 | 0.629 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.635 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.657 |
LIG_deltaCOP1_diTrp_1 | 75 | 82 | PF00928 | 0.292 |
LIG_eIF4E_1 | 137 | 143 | PF01652 | 0.485 |
LIG_FAT_LD_1 | 200 | 208 | PF03623 | 0.561 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.357 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 31 | 42 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.504 |
LIG_NRBOX | 199 | 205 | PF00104 | 0.561 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.485 |
LIG_NRBOX | 84 | 90 | PF00104 | 0.424 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.374 |
LIG_REV1ctd_RIR_1 | 108 | 118 | PF16727 | 0.355 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 217 | 220 | PF00017 | 0.272 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.656 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.408 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 198 | 204 | PF11976 | 0.627 |
LIG_SUMO_SIM_anti_2 | 33 | 39 | PF11976 | 0.657 |
LIG_SUMO_SIM_anti_2 | 97 | 105 | PF11976 | 0.535 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.420 |
LIG_TYR_ITIM | 215 | 220 | PF00017 | 0.444 |
MOD_CDC14_SPxK_1 | 50 | 53 | PF00782 | 0.674 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 47 | 53 | PF00069 | 0.680 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.429 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.686 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.653 |
MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.484 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.670 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.195 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.664 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.704 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.401 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.508 |
MOD_PK_1 | 170 | 176 | PF00069 | 0.569 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.523 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.715 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.645 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.726 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.719 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.395 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.389 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.438 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.648 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.672 |
TRG_DiLeu_BaEn_1 | 198 | 203 | PF01217 | 0.661 |
TRG_DiLeu_BaEn_4 | 195 | 201 | PF01217 | 0.693 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBC2 | Leptomonas seymouri | 66% | 100% |
A0A0S4JA41 | Bodo saltans | 28% | 100% |
A0A1X0NGU0 | Trypanosomatidae | 36% | 100% |
A0A3S5H5V0 | Leishmania donovani | 94% | 100% |
A4H4T7 | Leishmania braziliensis | 85% | 100% |
A4HT17 | Leishmania infantum | 94% | 100% |
C9ZTQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4QIV0 | Leishmania major | 92% | 100% |