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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4H5A9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.475 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.444 |
DEG_MDM2_SWIB_1 | 124 | 131 | PF02201 | 0.389 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.576 |
DOC_MAPK_FxFP_2 | 67 | 70 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 103 | 110 | PF00069 | 0.621 |
DOC_MAPK_NFAT4_5 | 103 | 111 | PF00069 | 0.622 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.449 |
LIG_14-3-3_CanoR_1 | 107 | 117 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.602 |
LIG_APCC_ABBA_1 | 60 | 65 | PF00400 | 0.641 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.289 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.602 |
LIG_deltaCOP1_diTrp_1 | 141 | 147 | PF00928 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 183 | 188 | PF00928 | 0.458 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.620 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.459 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.533 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.571 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.610 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.577 |
LIG_KLC1_Yacidic_2 | 163 | 168 | PF13176 | 0.423 |
LIG_LIR_Apic_2 | 168 | 173 | PF02991 | 0.418 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 65 | 70 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.649 |
LIG_MYND_3 | 157 | 161 | PF01753 | 0.423 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.399 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.378 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.378 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.720 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 166 | 169 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.627 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.404 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.682 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.640 |
LIG_SH3_4 | 189 | 196 | PF00018 | 0.447 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.615 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.562 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.241 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.603 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.727 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.615 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.567 |
MOD_CMANNOS | 117 | 120 | PF00535 | 0.335 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.495 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.453 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.358 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.723 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.611 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.584 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.393 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.607 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.355 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.355 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.659 |
MOD_PK_1 | 82 | 88 | PF00069 | 0.615 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.600 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.581 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.615 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.602 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.482 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.335 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.671 |
MOD_SUMO_rev_2 | 31 | 36 | PF00179 | 0.679 |
MOD_SUMO_rev_2 | 72 | 79 | PF00179 | 0.652 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.670 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P933 | Leptomonas seymouri | 81% | 99% |
A0A0S4IVJ7 | Bodo saltans | 67% | 100% |
A0A1X0NP20 | Trypanosomatidae | 73% | 100% |
A0A3S5H645 | Leishmania donovani | 90% | 100% |
A4HTI8 | Leishmania infantum | 90% | 100% |
C9ZPJ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9AMB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QID2 | Leishmania major | 89% | 100% |
V5DHY0 | Trypanosoma cruzi | 72% | 100% |