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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3S7X783
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.751 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 166 | 172 | PF00082 | 0.744 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.790 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.712 |
DOC_ANK_TNKS_1 | 199 | 206 | PF00023 | 0.682 |
DOC_MAPK_gen_1 | 129 | 137 | PF00069 | 0.702 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.610 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.745 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.676 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.687 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.707 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.779 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.729 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.690 |
LIG_LIR_Apic_2 | 260 | 265 | PF02991 | 0.780 |
LIG_LIR_Apic_2 | 83 | 89 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 150 | 160 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 285 | 293 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.672 |
LIG_MLH1_MIPbox_1 | 122 | 126 | PF16413 | 0.687 |
LIG_REV1ctd_RIR_1 | 123 | 133 | PF16727 | 0.690 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.612 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.710 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.679 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.597 |
LIG_SH2_GRB2like | 286 | 289 | PF00017 | 0.689 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.654 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.721 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.765 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.638 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.629 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.656 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.647 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.790 |
LIG_TYR_ITSM | 207 | 214 | PF00017 | 0.667 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.647 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.695 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.669 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.655 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.712 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.700 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.727 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.719 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.651 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.654 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.649 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.703 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.700 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.694 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.690 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.700 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.751 |
MOD_PK_1 | 120 | 126 | PF00069 | 0.758 |
MOD_PK_1 | 96 | 102 | PF00069 | 0.667 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.717 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.715 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.665 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.700 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.717 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.689 |
MOD_Plk_2-3 | 291 | 297 | PF00069 | 0.779 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.690 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.768 |
MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.700 |
TRG_DiLeu_BaEn_4 | 151 | 157 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.697 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.637 |
TRG_NLS_Bipartite_1 | 200 | 221 | PF00514 | 0.747 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.673 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS4 | Leptomonas seymouri | 54% | 98% |
A0A1X0NRB6 | Trypanosomatidae | 30% | 100% |
A4HM03 | Leishmania braziliensis | 66% | 100% |
A4I9D4 | Leishmania infantum | 100% | 100% |
E9B4D4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q3P3 | Leishmania major | 93% | 100% |