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: A4HT11
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.802 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 304 | 310 | PF00082 | 0.713 |
CLV_PCSK_PC7_1 | 59 | 65 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.740 |
DEG_APCC_DBOX_1 | 386 | 394 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.591 |
DOC_ANK_TNKS_1 | 21 | 28 | PF00023 | 0.530 |
DOC_CYCLIN_RxL_1 | 330 | 341 | PF00134 | 0.654 |
DOC_MAPK_FxFP_2 | 2 | 5 | PF00069 | 0.588 |
DOC_PP1_RVXF_1 | 331 | 338 | PF00149 | 0.630 |
DOC_PP1_RVXF_1 | 377 | 383 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.613 |
DOC_PP4_FxxP_1 | 2 | 5 | PF00568 | 0.652 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.353 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 386 | 391 | PF00244 | 0.600 |
LIG_APCC_ABBA_1 | 276 | 281 | PF00400 | 0.741 |
LIG_APCC_ABBAyCdc20_2 | 333 | 339 | PF00400 | 0.606 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.613 |
LIG_Clathr_ClatBox_1 | 219 | 223 | PF01394 | 0.556 |
LIG_CtBP_PxDLS_1 | 365 | 369 | PF00389 | 0.606 |
LIG_DLG_GKlike_1 | 386 | 393 | PF00625 | 0.587 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.534 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.763 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.679 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.657 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.601 |
LIG_Integrin_RGD_1 | 296 | 298 | PF01839 | 0.697 |
LIG_Integrin_RGD_1 | 311 | 313 | PF01839 | 0.630 |
LIG_IRF3_LxIS_1 | 41 | 46 | PF10401 | 0.670 |
LIG_LIR_Gen_1 | 389 | 394 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.571 |
LIG_LYPXL_yS_3 | 4 | 7 | PF13949 | 0.598 |
LIG_PDZ_Class_1 | 389 | 394 | PF00595 | 0.549 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.470 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.495 |
LIG_SH2_PTP2 | 6 | 9 | PF00017 | 0.581 |
LIG_SH2_SRC | 6 | 9 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.738 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.581 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.605 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.632 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.663 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.685 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.654 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.800 |
LIG_TRAF2_2 | 21 | 26 | PF00917 | 0.586 |
LIG_TYR_ITIM | 112 | 117 | PF00017 | 0.494 |
MOD_CDK_SPK_2 | 347 | 352 | PF00069 | 0.723 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.724 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.605 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.647 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.588 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.545 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.680 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.515 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.762 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.605 |
MOD_Cter_Amidation | 323 | 326 | PF01082 | 0.780 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.723 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.675 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.612 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.532 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.758 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.583 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.778 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.644 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.641 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.657 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.656 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.632 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.668 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.743 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.714 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.693 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.805 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.605 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.710 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.795 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.639 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.616 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.583 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.662 |
MOD_PKB_1 | 309 | 317 | PF00069 | 0.774 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.570 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.622 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.600 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.606 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.759 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.646 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.658 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.580 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.604 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.741 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.665 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.628 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.726 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.777 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.623 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.498 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.619 |
TRG_NLS_MonoExtC_3 | 307 | 313 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.747 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4J6 | Leptomonas seymouri | 40% | 100% |
A0A3S5H5U8 | Leishmania donovani | 99% | 100% |
A4H4T2 | Leishmania braziliensis | 70% | 100% |
E9AKZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QIV6 | Leishmania major | 89% | 100% |