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: A0A3S7WU02
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.609 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.677 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.708 |
CLV_Separin_Metazoa | 232 | 236 | PF03568 | 0.515 |
DEG_APCC_KENBOX_2 | 260 | 264 | PF00400 | 0.731 |
DEG_SPOP_SBC_1 | 267 | 271 | PF00917 | 0.745 |
DOC_CYCLIN_RxL_1 | 74 | 83 | PF00134 | 0.670 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.653 |
DOC_PP1_RVXF_1 | 137 | 143 | PF00149 | 0.608 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.682 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.616 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.671 |
LIG_EH_1 | 31 | 35 | PF12763 | 0.634 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.648 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.705 |
LIG_LIR_Apic_2 | 164 | 169 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 104 | 110 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.543 |
LIG_PDZ_Class_3 | 292 | 297 | PF00595 | 0.701 |
LIG_Pex14_1 | 102 | 106 | PF04695 | 0.576 |
LIG_Rb_LxCxE_1 | 116 | 137 | PF01857 | 0.563 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.648 |
LIG_SH3_1 | 166 | 172 | PF00018 | 0.725 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.665 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.663 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.678 |
LIG_SUMO_SIM_par_1 | 34 | 41 | PF11976 | 0.628 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.723 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.630 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.762 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.591 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.764 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.773 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.560 |
MOD_Cter_Amidation | 189 | 192 | PF01082 | 0.684 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.705 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.811 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.476 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.700 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.714 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.715 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.700 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.609 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.637 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.697 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.560 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.769 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.562 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.717 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.523 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.585 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.643 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.729 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.678 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.676 |
MOD_OFUCOSY | 64 | 70 | PF10250 | 0.647 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.638 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.679 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.573 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.699 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.599 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.577 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.471 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.657 |
MOD_PKB_1 | 191 | 199 | PF00069 | 0.677 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.770 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.756 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.683 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.791 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.617 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P756 | Leptomonas seymouri | 35% | 95% |
A4H8L3 | Leishmania braziliensis | 70% | 100% |
E9AGN6 | Leishmania infantum | 99% | 100% |
E9AQP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QES9 | Leishmania major | 87% | 100% |