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: A4I4T1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.718 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.546 |
CLV_PCSK_FUR_1 | 70 | 74 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.552 |
DEG_COP1_1 | 255 | 263 | PF00400 | 0.573 |
DEG_SPOP_SBC_1 | 332 | 336 | PF00917 | 0.734 |
DOC_CYCLIN_yClb1_LxF_4 | 155 | 161 | PF00134 | 0.464 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 52 | 58 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 70 | 77 | PF00149 | 0.396 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.669 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.703 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.665 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.623 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.726 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.562 |
LIG_Clathr_ClatBox_1 | 55 | 59 | PF01394 | 0.438 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.748 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.453 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.737 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.441 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.643 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.562 |
LIG_SH2_SRC | 201 | 204 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.418 |
LIG_SH3_1 | 201 | 207 | PF00018 | 0.677 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.594 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.679 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.666 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.696 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.769 |
LIG_SUMO_SIM_par_1 | 308 | 315 | PF11976 | 0.719 |
LIG_SUMO_SIM_par_1 | 35 | 41 | PF11976 | 0.366 |
LIG_TRFH_1 | 292 | 296 | PF08558 | 0.686 |
LIG_UBA3_1 | 36 | 42 | PF00899 | 0.591 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.459 |
LIG_WW_3 | 354 | 358 | PF00397 | 0.543 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.664 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.650 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.749 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.652 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.642 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.700 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.683 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.723 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.462 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.485 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.735 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.470 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.710 |
MOD_GlcNHglycan | 224 | 228 | PF01048 | 0.699 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.671 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.699 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.648 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.605 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.789 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.690 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.442 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.557 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.756 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.745 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.664 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.716 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.756 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.669 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.705 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.539 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.584 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.765 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.680 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.543 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.787 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.737 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.570 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.450 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.444 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.521 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.572 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.631 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.479 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.762 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.716 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.690 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.644 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.740 |
MOD_SUMO_for_1 | 95 | 98 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 11 | 21 | PF00179 | 0.692 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.679 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.655 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.390 |
TRG_NLS_Bipartite_1 | 72 | 91 | PF00514 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3W2 | Leptomonas seymouri | 43% | 66% |
A0A3Q8IFH8 | Leishmania donovani | 99% | 100% |
A4HHU4 | Leishmania braziliensis | 57% | 100% |
E9AE84 | Leishmania major | 90% | 100% |
E9ALK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |