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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AE07
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.445 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.612 |
DOC_CYCLIN_RxL_1 | 38 | 46 | PF00134 | 0.636 |
DOC_CYCLIN_yClb1_LxF_4 | 39 | 44 | PF00134 | 0.602 |
DOC_MAPK_FxFP_2 | 45 | 48 | PF00069 | 0.703 |
DOC_MAPK_gen_1 | 190 | 198 | PF00069 | 0.795 |
DOC_MAPK_MEF2A_6 | 109 | 118 | PF00069 | 0.768 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.637 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.772 |
DOC_PP2B_PxIxI_1 | 113 | 119 | PF00149 | 0.764 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.623 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.704 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.644 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.657 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.728 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.740 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.339 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.556 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.727 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.573 |
LIG_LIR_Apic_2 | 66 | 71 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.735 |
LIG_Pex14_1 | 224 | 228 | PF04695 | 0.633 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.712 |
LIG_SH2_PTP2 | 68 | 71 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.616 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 115 | 121 | PF11976 | 0.764 |
LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.336 |
LIG_WW_3 | 38 | 42 | PF00397 | 0.633 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.735 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.623 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.269 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.605 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.646 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.740 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.508 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.586 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.500 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.413 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.450 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.433 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.816 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.766 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.614 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.633 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.618 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.635 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.818 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.410 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.765 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.591 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.698 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.647 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.750 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.443 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.647 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.663 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.704 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.659 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.701 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.622 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.764 |
MOD_PKB_1 | 83 | 91 | PF00069 | 0.694 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.410 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.729 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.497 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.622 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.818 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.557 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.699 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.650 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.633 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7L3 | Leishmania donovani | 80% | 96% |
A4HHG0 | Leishmania braziliensis | 53% | 78% |
A4I4L0 | Leishmania infantum | 80% | 96% |
E9ALS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 96% |