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: E9AW50
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 322 | 326 | PF00656 | 0.800 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.715 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.690 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.788 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.621 |
CLV_Separin_Metazoa | 216 | 220 | PF03568 | 0.364 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.554 |
DOC_ANK_TNKS_1 | 320 | 327 | PF00023 | 0.551 |
DOC_CYCLIN_RxL_1 | 237 | 248 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 89 | 95 | PF00069 | 0.717 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.655 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.742 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 272 | 281 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.811 |
LIG_Actin_WH2_2 | 197 | 214 | PF00022 | 0.499 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.791 |
LIG_EVH1_1 | 158 | 162 | PF00568 | 0.650 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.778 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.480 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.531 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.541 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.746 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.796 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.619 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.738 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.757 |
LIG_LIR_Apic_2 | 123 | 127 | PF02991 | 0.799 |
LIG_MYND_1 | 163 | 167 | PF01753 | 0.725 |
LIG_PDZ_Class_2 | 345 | 350 | PF00595 | 0.679 |
LIG_SH2_PTP2 | 82 | 85 | PF00017 | 0.611 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.611 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.727 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.660 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.557 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.754 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.590 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.671 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.619 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.485 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.780 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.545 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.468 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.607 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.775 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.686 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.552 |
MOD_GlcNHglycan | 100 | 104 | PF01048 | 0.742 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.675 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.673 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.824 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.710 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.818 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.675 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.504 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.712 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.692 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.451 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.804 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.798 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.492 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.663 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.709 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.594 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.786 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.584 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.676 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.737 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.818 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.753 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.498 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.657 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.794 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.535 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.737 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.695 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.689 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.705 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.532 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.751 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.811 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.673 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.733 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.755 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_2 | 343 | 349 | PF01217 | 0.683 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.791 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.682 |
TRG_NLS_MonoExtC_3 | 239 | 245 | PF00514 | 0.733 |
TRG_NLS_MonoExtN_4 | 238 | 244 | PF00514 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.786 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9J6 | Leptomonas seymouri | 33% | 100% |
A0A3S7WXL1 | Leishmania donovani | 84% | 100% |
A4HCR1 | Leishmania braziliensis | 64% | 98% |
A4I086 | Leishmania infantum | 84% | 100% |
Q4QBC7 | Leishmania major | 84% | 100% |