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: E9AXU9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.756 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.586 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.742 |
DEG_SCF_FBW7_1 | 227 | 234 | PF00400 | 0.661 |
DOC_MAPK_gen_1 | 151 | 161 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 154 | 161 | PF00069 | 0.331 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.800 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.597 |
LIG_Actin_RPEL_3 | 174 | 193 | PF02755 | 0.514 |
LIG_Actin_WH2_2 | 4 | 21 | PF00022 | 0.606 |
LIG_Clathr_ClatBox_1 | 173 | 177 | PF01394 | 0.359 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.465 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.696 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.526 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.705 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.493 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.668 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.613 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.563 |
LIG_Rb_LxCxE_1 | 182 | 202 | PF01857 | 0.589 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.572 |
MOD_CDK_SPxxK_3 | 78 | 85 | PF00069 | 0.805 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.536 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.626 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.474 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.783 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.739 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.625 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.660 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.623 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.528 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.639 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.608 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.670 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.784 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.409 |
MOD_GlcNHglycan | 165 | 170 | PF01048 | 0.543 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.411 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.504 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.648 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.480 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.526 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.566 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.609 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.796 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.678 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.715 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.391 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.611 |
MOD_N-GLC_2 | 25 | 27 | PF02516 | 0.461 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.358 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.483 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.551 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.783 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.653 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.686 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.765 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.800 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.572 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.532 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.436 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.687 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.666 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.788 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.736 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.804 |
MOD_SUMO_rev_2 | 206 | 215 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYI0 | Leptomonas seymouri | 33% | 100% |
A0A3Q8INN7 | Leishmania donovani | 84% | 100% |
A4HEB9 | Leishmania braziliensis | 65% | 100% |
A4I1R4 | Leishmania infantum | 82% | 100% |
Q4Q9M2 | Leishmania major | 85% | 100% |