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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A0A3Q8IAW3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.792 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.802 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.792 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.802 |
CLV_PCSK_PC7_1 | 212 | 218 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.718 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.697 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.711 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.760 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.743 |
DOC_CDC14_PxL_1 | 350 | 358 | PF14671 | 0.715 |
DOC_CYCLIN_RxL_1 | 163 | 171 | PF00134 | 0.737 |
DOC_MAPK_gen_1 | 358 | 367 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.638 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.697 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 14 | 24 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.804 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 399 | 408 | PF00244 | 0.751 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.731 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.665 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.662 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.677 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.703 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.692 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.679 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.758 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.766 |
LIG_LIR_Gen_1 | 317 | 325 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 374 | 384 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 421 | 425 | PF02991 | 0.745 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.814 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.745 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.786 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.546 |
LIG_PCNA_PIPBox_1 | 100 | 109 | PF02747 | 0.700 |
LIG_PCNA_yPIPBox_3 | 322 | 333 | PF02747 | 0.638 |
LIG_Pex3_1 | 116 | 127 | PF04882 | 0.529 |
LIG_SH2_PTP2 | 318 | 321 | PF00017 | 0.699 |
LIG_SH2_SRC | 208 | 211 | PF00017 | 0.760 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.752 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.752 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.613 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.677 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.643 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.481 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.718 |
LIG_SH3_5 | 334 | 338 | PF00018 | 0.759 |
MOD_CDK_SPxxK_3 | 274 | 281 | PF00069 | 0.746 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.809 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.795 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.803 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.596 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.781 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.721 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.774 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.699 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.661 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.809 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.663 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.444 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.761 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.746 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.779 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.766 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.706 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.631 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.766 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.635 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.740 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.796 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.703 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.693 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.757 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.785 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.629 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.736 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.457 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.630 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.716 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.689 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.616 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.746 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.727 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.706 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.794 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.686 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.720 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.664 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.608 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.804 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.664 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.626 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.664 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.746 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.661 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.631 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.542 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.701 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.635 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.718 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.665 |
MOD_SUMO_rev_2 | 210 | 218 | PF00179 | 0.761 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.689 |
TRG_DiLeu_LyEn_5 | 248 | 253 | PF01217 | 0.700 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.752 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.810 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.699 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.749 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR9 | Leptomonas seymouri | 36% | 96% |
E9AGV7 | Leishmania infantum | 99% | 100% |
E9AV73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 97% |
Q4QCA8 | Leishmania major | 89% | 100% |