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: A4HDU1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.627 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.690 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.750 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.750 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.779 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.515 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.692 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.516 |
LIG_Actin_WH2_2 | 141 | 157 | PF00022 | 0.739 |
LIG_Actin_WH2_2 | 50 | 66 | PF00022 | 0.653 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.513 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.674 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.533 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 2 | 8 | PF02991 | 0.705 |
LIG_LIR_Gen_1 | 219 | 225 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.535 |
LIG_NRBOX | 182 | 188 | PF00104 | 0.490 |
LIG_PTB_Apo_2 | 155 | 162 | PF02174 | 0.467 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.772 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.772 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.764 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.716 |
LIG_SUMO_SIM_anti_2 | 139 | 146 | PF11976 | 0.612 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.560 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.642 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.497 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.629 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.516 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.616 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.700 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.694 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.732 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.734 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.630 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.596 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.660 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.762 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.676 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.642 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.702 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.720 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.631 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.775 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.604 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.558 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.637 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.573 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.731 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.754 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.606 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.773 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.481 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.559 |
MOD_N-GLC_2 | 87 | 89 | PF02516 | 0.535 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.676 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.699 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.530 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.681 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.741 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.501 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.730 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.509 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.514 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.695 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.688 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.480 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.627 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.656 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.511 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.740 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.513 |
MOD_SUMO_rev_2 | 190 | 200 | PF00179 | 0.678 |
TRG_DiLeu_BaEn_2 | 8 | 14 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.755 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C0 | Leptomonas seymouri | 29% | 100% |
A0A3S7WYM3 | Leishmania donovani | 60% | 100% |
A4I138 | Leishmania infantum | 60% | 100% |
E9AX76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QAA0 | Leishmania major | 62% | 100% |