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: Q4QCA8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.788 |
CLV_PCSK_FUR_1 | 13 | 17 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.800 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.788 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.800 |
CLV_PCSK_PC7_1 | 212 | 218 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.725 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.713 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.743 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.758 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.744 |
DOC_CDC14_PxL_1 | 350 | 358 | PF14671 | 0.705 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.601 |
DOC_CYCLIN_RxL_1 | 163 | 171 | PF00134 | 0.766 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.589 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.673 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.610 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.575 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 14 | 24 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.759 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.727 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.671 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.641 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.598 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.676 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.695 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.630 |
LIG_LIR_Apic_2 | 126 | 131 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.764 |
LIG_LIR_Gen_1 | 317 | 325 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 374 | 384 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 419 | 423 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.811 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 419 | 423 | PF02991 | 0.658 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.780 |
LIG_MYND_1 | 354 | 358 | PF01753 | 0.553 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.618 |
LIG_PCNA_PIPBox_1 | 100 | 109 | PF02747 | 0.713 |
LIG_PCNA_yPIPBox_3 | 322 | 333 | PF02747 | 0.600 |
LIG_SH2_PTP2 | 318 | 321 | PF00017 | 0.678 |
LIG_SH2_SRC | 208 | 211 | PF00017 | 0.771 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.705 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.745 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.778 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.575 |
LIG_SH3_1 | 355 | 361 | PF00018 | 0.546 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.605 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.730 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.666 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.677 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.517 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.738 |
LIG_SH3_5 | 334 | 338 | PF00018 | 0.742 |
MOD_CDK_SPxxK_3 | 274 | 281 | PF00069 | 0.736 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.733 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.791 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.789 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.696 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.690 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.548 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.564 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.758 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.642 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.656 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.797 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.704 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.773 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.747 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.687 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.650 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.630 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.664 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.661 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.708 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.714 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.670 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.749 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.777 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.602 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.644 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.553 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.475 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.604 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.785 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.705 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.567 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.727 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.698 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.758 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.614 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.727 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.669 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.701 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.738 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.733 |
MOD_PKA_1 | 14 | 20 | PF00069 | 0.576 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.641 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.756 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.641 |
MOD_PKB_1 | 13 | 21 | PF00069 | 0.577 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.539 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.698 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.748 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.606 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.603 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.755 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.680 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.619 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.710 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.653 |
MOD_SUMO_rev_2 | 210 | 218 | PF00179 | 0.763 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.724 |
TRG_DiLeu_LyEn_5 | 248 | 253 | PF01217 | 0.727 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.778 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.821 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.678 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.760 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.617 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR9 | Leptomonas seymouri | 36% | 95% |
A0A3Q8IAW3 | Leishmania donovani | 89% | 100% |
E9AGV7 | Leishmania infantum | 88% | 100% |
E9AV73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |