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: E9B3V9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.811 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.771 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.811 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.811 |
CLV_PCSK_PC7_1 | 381 | 387 | PF00082 | 0.701 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.547 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.842 |
DOC_MAPK_MEF2A_6 | 46 | 54 | PF00069 | 0.809 |
DOC_PP2B_LxvP_1 | 204 | 207 | PF13499 | 0.844 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.619 |
DOC_PP4_FxxP_1 | 388 | 391 | PF00568 | 0.726 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.755 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.807 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.819 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.842 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.659 |
LIG_14-3-3_CanoR_1 | 351 | 360 | PF00244 | 0.793 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.770 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.804 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.845 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.807 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.653 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.468 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.790 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.740 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.727 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.791 |
LIG_Pex14_1 | 318 | 322 | PF04695 | 0.749 |
LIG_Pex14_1 | 369 | 373 | PF04695 | 0.747 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.688 |
LIG_SH2_STAT3 | 322 | 325 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.655 |
LIG_SH3_2 | 298 | 303 | PF14604 | 0.534 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.644 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.711 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.592 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.641 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.828 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.788 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.503 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.813 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.766 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.771 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.515 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.550 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.519 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.851 |
LIG_TRFH_1 | 269 | 273 | PF08558 | 0.623 |
LIG_TRFH_1 | 322 | 326 | PF08558 | 0.742 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.650 |
LIG_WW_1 | 142 | 145 | PF00397 | 0.537 |
LIG_WW_2 | 191 | 194 | PF00397 | 0.570 |
MOD_CDK_SPK_2 | 82 | 87 | PF00069 | 0.853 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.765 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.713 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.719 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.705 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.612 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.853 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.466 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.596 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.732 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.730 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.838 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.686 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.801 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.694 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.737 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.682 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.630 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.755 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.839 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.835 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.558 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.549 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.779 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.705 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.604 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.757 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.761 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.556 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.815 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.549 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.680 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.547 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.853 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.637 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.656 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.799 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.674 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.832 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.748 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.547 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.732 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.606 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.710 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.775 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.683 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.842 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.662 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.789 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.763 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.681 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.761 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.772 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 68 | 77 | PF00179 | 0.779 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.711 |
TRG_NLS_MonoCore_2 | 302 | 307 | PF00514 | 0.809 |
TRG_NLS_MonoExtC_3 | 303 | 308 | PF00514 | 0.674 |
TRG_NLS_MonoExtN_4 | 300 | 307 | PF00514 | 0.807 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITZ0 | Leishmania donovani | 87% | 70% |
A4I8Z0 | Leishmania infantum | 87% | 98% |
Q4Q465 | Leishmania major | 83% | 100% |