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: A0A3S7X9Q8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.754 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.569 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.656 |
DOC_CYCLIN_yCln2_LP_2 | 413 | 419 | PF00134 | 0.709 |
DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.599 |
DOC_PP1_RVXF_1 | 185 | 191 | PF00149 | 0.767 |
DOC_PP1_SILK_1 | 297 | 302 | PF00149 | 0.697 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 108 | 112 | PF12436 | 0.781 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 174 | 191 | PF00022 | 0.642 |
LIG_Actin_WH2_2 | 288 | 303 | PF00022 | 0.705 |
LIG_APCC_ABBA_1 | 167 | 172 | PF00400 | 0.700 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
LIG_BIR_III_4 | 122 | 126 | PF00653 | 0.804 |
LIG_CaM_NSCaTE_8 | 296 | 303 | PF13499 | 0.693 |
LIG_deltaCOP1_diTrp_1 | 143 | 152 | PF00928 | 0.671 |
LIG_deltaCOP1_diTrp_1 | 376 | 380 | PF00928 | 0.712 |
LIG_eIF4E_1 | 278 | 284 | PF01652 | 0.704 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.700 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.641 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.657 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.641 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.760 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.546 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.664 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.674 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.727 |
LIG_GBD_Chelix_1 | 180 | 188 | PF00786 | 0.663 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 92 | 97 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 243 | 254 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 407 | 417 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.527 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.534 |
LIG_Rb_LxCxE_1 | 330 | 352 | PF01857 | 0.748 |
LIG_Rb_pABgroove_1 | 240 | 248 | PF01858 | 0.620 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.568 |
LIG_SH2_PTP2 | 71 | 74 | PF00017 | 0.582 |
LIG_SH2_SRC | 356 | 359 | PF00017 | 0.655 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.652 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.582 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.597 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.644 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.459 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 381 | 387 | PF11976 | 0.716 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.608 |
LIG_UBA3_1 | 245 | 251 | PF00899 | 0.717 |
LIG_WRC_WIRS_1 | 328 | 333 | PF05994 | 0.597 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.740 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.760 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.601 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.789 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.500 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.557 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.682 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.630 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.704 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.677 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.642 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.558 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.648 |
MOD_GlcNHglycan | 126 | 130 | PF01048 | 0.708 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.595 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.541 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.653 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.675 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.525 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.639 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.621 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.679 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.538 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.611 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.684 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.772 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.711 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.569 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.582 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.699 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.711 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.638 |
MOD_LATS_1 | 38 | 44 | PF00433 | 0.521 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.647 |
MOD_N-GLC_2 | 142 | 144 | PF02516 | 0.687 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.633 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.557 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.593 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.727 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.658 |
MOD_PK_1 | 40 | 46 | PF00069 | 0.517 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.633 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.635 |
MOD_PKB_1 | 372 | 380 | PF00069 | 0.630 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.614 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.656 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.656 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.706 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.669 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.588 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.709 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.551 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.637 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.700 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.594 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.698 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.713 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.768 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P5 | Leptomonas seymouri | 37% | 90% |
A4HN22 | Leishmania braziliensis | 73% | 100% |
A4IBP6 | Leishmania infantum | 100% | 100% |
E9AFH7 | Leishmania major | 90% | 100% |
E9B6N2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |