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: A4HEB9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.524 |
CLV_Separin_Metazoa | 191 | 195 | PF03568 | 0.348 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.377 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.756 |
DEG_SCF_FBW7_1 | 226 | 233 | PF00400 | 0.655 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.682 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.359 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.359 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.331 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.532 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.645 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.478 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.459 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.677 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.500 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.626 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.350 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.569 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.504 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 106 | 112 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 39 | 46 | PF11976 | 0.515 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.349 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.514 |
MOD_CDK_SPxxK_3 | 78 | 85 | PF00069 | 0.785 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.510 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.613 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.763 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.612 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.618 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.434 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.469 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.679 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.778 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.345 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.405 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.483 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.603 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.637 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.730 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.669 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.706 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.541 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.525 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.435 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.763 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.679 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.592 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.348 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.727 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.790 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.580 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.470 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.528 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.579 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.517 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.663 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.770 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.699 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.784 |
MOD_SUMO_rev_2 | 110 | 119 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.503 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.580 |
TRG_NES_CRM1_1 | 13 | 26 | PF08389 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 19 | 24 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYI0 | Leptomonas seymouri | 33% | 100% |
A0A3Q8INN7 | Leishmania donovani | 65% | 100% |
A4I1R4 | Leishmania infantum | 65% | 100% |
E9AXU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q9M2 | Leishmania major | 68% | 100% |