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: A0A3Q8IDN0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.808 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.676 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.825 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.683 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.582 |
DEG_COP1_1 | 250 | 260 | PF00400 | 0.744 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.665 |
DOC_MAPK_MEF2A_6 | 151 | 158 | PF00069 | 0.572 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.741 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.843 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.576 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.703 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.668 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.623 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.518 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.651 |
LIG_GBD_Chelix_1 | 66 | 74 | PF00786 | 0.450 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.718 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.666 |
LIG_Pex14_1 | 210 | 214 | PF04695 | 0.685 |
LIG_RPA_C_Fungi | 57 | 69 | PF08784 | 0.475 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.584 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.685 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.770 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.644 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.751 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.625 |
MOD_CDK_SPxxK_3 | 15 | 22 | PF00069 | 0.594 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.565 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.702 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.577 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.649 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.684 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.750 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.557 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.608 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.629 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.750 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.654 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.480 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.726 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.780 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.613 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.766 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.627 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.707 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.671 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.633 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.748 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.801 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.713 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.624 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.662 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.725 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.563 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.612 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.657 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.787 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.539 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.657 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.736 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.665 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.642 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.749 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.843 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.623 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.679 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.604 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.791 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.807 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M0 | Leptomonas seymouri | 41% | 87% |
A4HEL4 | Leishmania braziliensis | 63% | 100% |
A4I1U5 | Leishmania infantum | 99% | 100% |
E9AXY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q9I5 | Leishmania major | 89% | 100% |