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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QJG5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.737 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.804 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.677 |
CLV_PCSK_PC7_1 | 33 | 39 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.684 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.839 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.727 |
DEG_SPOP_SBC_1 | 254 | 258 | PF00917 | 0.664 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 246 | 254 | PF00069 | 0.572 |
DOC_MAPK_NFAT4_5 | 247 | 255 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.646 |
DOC_PP4_FxxP_1 | 12 | 15 | PF00568 | 0.786 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.713 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.754 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.839 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.713 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 85 | 94 | PF00244 | 0.828 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.814 |
LIG_Clathr_ClatBox_1 | 132 | 136 | PF01394 | 0.757 |
LIG_eIF4E_1 | 16 | 22 | PF01652 | 0.662 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.760 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.661 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.572 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.694 |
LIG_IBAR_NPY_1 | 14 | 16 | PF08397 | 0.779 |
LIG_LIR_Apic_2 | 10 | 15 | PF02991 | 0.790 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.596 |
LIG_MAD2 | 129 | 137 | PF02301 | 0.715 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.764 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.651 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.650 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.658 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.760 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.611 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.752 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.737 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.691 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.773 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.759 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.702 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.798 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.833 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.797 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.729 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.596 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.697 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.640 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.716 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.641 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.784 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.618 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.680 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.741 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.669 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.687 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.595 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.654 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.703 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.741 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.747 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.679 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.599 |
MOD_Plk_2-3 | 162 | 168 | PF00069 | 0.557 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.658 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.807 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.817 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.611 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.708 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.703 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3H3 | Leptomonas seymouri | 36% | 100% |
A0A3S7WP10 | Leishmania donovani | 91% | 100% |
A4H482 | Leishmania braziliensis | 67% | 98% |
A4HSF9 | Leishmania infantum | 91% | 100% |
E9AKE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |