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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: Q4Q7Z9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.617 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.698 |
CLV_PCSK_PC7_1 | 344 | 350 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.661 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.629 |
DEG_SCF_FBW7_1 | 232 | 237 | PF00400 | 0.675 |
DEG_SCF_FBW7_1 | 389 | 394 | PF00400 | 0.684 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.655 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.675 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.677 |
DOC_CKS1_1 | 306 | 311 | PF01111 | 0.656 |
DOC_MAPK_DCC_7 | 238 | 247 | PF00069 | 0.687 |
DOC_MAPK_HePTP_8 | 235 | 247 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 238 | 247 | PF00069 | 0.687 |
DOC_MAPK_RevD_3 | 336 | 349 | PF00069 | 0.590 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.630 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 179 | 182 | PF13499 | 0.678 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.791 |
DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.562 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.679 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 296 | 306 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 426 | 431 | PF00244 | 0.600 |
LIG_AP2alpha_2 | 220 | 222 | PF02296 | 0.692 |
LIG_BIR_III_2 | 24 | 28 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.638 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.642 |
LIG_deltaCOP1_diTrp_1 | 364 | 374 | PF00928 | 0.614 |
LIG_EVH1_2 | 243 | 247 | PF00568 | 0.553 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.605 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.689 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.679 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.712 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.649 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.710 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.733 |
LIG_Integrin_RGD_1 | 395 | 397 | PF01839 | 0.659 |
LIG_LIR_Gen_1 | 61 | 69 | PF02991 | 0.757 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.754 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.647 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.653 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.623 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.526 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.742 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.753 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.588 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 327 | 333 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 426 | 431 | PF11976 | 0.554 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.673 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.716 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.649 |
LIG_WRC_WIRS_1 | 210 | 215 | PF05994 | 0.596 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.714 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.653 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.662 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.581 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.656 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.698 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.733 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.718 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.727 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.686 |
MOD_DYRK1A_RPxSP_1 | 387 | 391 | PF00069 | 0.686 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.695 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.721 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.649 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.721 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.622 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.666 |
MOD_GlcNHglycan | 398 | 404 | PF01048 | 0.637 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.681 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.597 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.834 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.678 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.609 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.655 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.709 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.752 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.655 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.827 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.650 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.633 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.656 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.603 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.662 |
MOD_PIKK_1 | 407 | 413 | PF00454 | 0.721 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.642 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.673 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.746 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.664 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.714 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.636 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.651 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.647 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.603 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.664 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.577 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.728 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.789 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.714 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.726 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.537 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.688 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.637 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.714 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.671 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.606 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.636 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.587 |
TRG_DiLeu_BaEn_1 | 423 | 428 | PF01217 | 0.649 |
TRG_DiLeu_BaEn_1 | 435 | 440 | PF01217 | 0.481 |
TRG_DiLeu_LyEn_5 | 423 | 428 | PF01217 | 0.649 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.767 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.743 |
TRG_ER_diArg_1 | 348 | 351 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.617 |
TRG_NLS_MonoExtC_3 | 137 | 142 | PF00514 | 0.742 |
TRG_NLS_MonoExtC_3 | 162 | 168 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 135 | 142 | PF00514 | 0.631 |
TRG_NLS_MonoExtN_4 | 160 | 167 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 418 | 422 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7K1 | Leishmania donovani | 88% | 95% |
A4HGW6 | Leishmania braziliensis | 55% | 93% |
E9B086 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |