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: Q4Q915
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.820 |
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.751 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.776 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.746 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.654 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.748 |
CLV_PCSK_PC7_1 | 311 | 317 | PF00082 | 0.765 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.641 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.743 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.751 |
DOC_CYCLIN_RxL_1 | 207 | 217 | PF00134 | 0.646 |
DOC_CYCLIN_RxL_1 | 218 | 226 | PF00134 | 0.508 |
DOC_PP1_RVXF_1 | 219 | 226 | PF00149 | 0.689 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.835 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 210 | 220 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.727 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.842 |
LIG_BIR_III_4 | 83 | 87 | PF00653 | 0.714 |
LIG_Clathr_ClatBox_1 | 222 | 226 | PF01394 | 0.619 |
LIG_CSL_BTD_1 | 191 | 194 | PF09270 | 0.671 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.710 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.604 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.692 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.817 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.784 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.765 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.714 |
LIG_PDZ_Class_3 | 376 | 381 | PF00595 | 0.754 |
LIG_Rb_LxCxE_1 | 174 | 190 | PF01857 | 0.768 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.638 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.656 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.699 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.778 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.726 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.831 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.756 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.835 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.588 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.738 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.640 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.758 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.617 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.708 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.622 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.787 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.692 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.617 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.644 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.597 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.630 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.777 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.762 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.700 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.843 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.785 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.751 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.700 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.751 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.619 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.686 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.509 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.595 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.693 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.831 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.512 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.740 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.631 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.657 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.670 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.431 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.362 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.735 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.626 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.655 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.828 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.593 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.501 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.789 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.841 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.599 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.696 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.755 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.713 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.660 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.749 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.756 |
MOD_PKB_1 | 315 | 323 | PF00069 | 0.771 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.754 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.710 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.683 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.632 |
MOD_Plk_2-3 | 37 | 43 | PF00069 | 0.726 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.719 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.644 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.835 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.800 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.581 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.586 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.722 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 218 | 223 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.755 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.672 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 221 | 226 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICW3 | Leishmania donovani | 87% | 100% |
A4I2B0 | Leishmania infantum | 88% | 100% |
E9AIQ9 | Leishmania braziliensis | 62% | 100% |
E9AYF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |