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: A0A3Q8IE62
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 159 | 163 | PF00917 | 0.590 |
DOC_CYCLIN_RxL_1 | 71 | 81 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 21 | 29 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 86 | 94 | PF00069 | 0.540 |
DOC_PP1_RVXF_1 | 237 | 244 | PF00149 | 0.480 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.620 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.548 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.473 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.529 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.563 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.624 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.643 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.630 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.614 |
LIG_REV1ctd_RIR_1 | 201 | 211 | PF16727 | 0.494 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.454 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.448 |
LIG_SH3_2 | 120 | 125 | PF14604 | 0.590 |
LIG_SH3_2 | 17 | 22 | PF14604 | 0.525 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.692 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 142 | 148 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 95 | 102 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.523 |
LIG_TYR_ITIM | 100 | 105 | PF00017 | 0.537 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.585 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.606 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.481 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.631 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.560 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.532 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.609 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.458 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.569 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.661 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.610 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.528 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.581 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.537 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.603 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.572 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.474 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.575 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.705 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.629 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.314 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.588 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.633 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.607 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.482 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.588 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.443 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.458 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.577 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.596 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.597 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.634 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.482 |
TRG_NES_CRM1_1 | 136 | 150 | PF08389 | 0.489 |
TRG_NLS_MonoExtN_4 | 122 | 129 | PF00514 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6I3 | Leptomonas seymouri | 50% | 95% |
A4HGZ0 | Leishmania braziliensis | 82% | 100% |
A4I422 | Leishmania infantum | 99% | 100% |
E9B0A9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q7X5 | Leishmania major | 93% | 100% |