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. | yes | yes: 10 |
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: Q4QBR7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.736 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.681 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.492 |
DOC_MAPK_gen_1 | 38 | 45 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 18 | 25 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 38 | 45 | PF00069 | 0.428 |
DOC_MAPK_NFAT4_5 | 18 | 26 | PF00069 | 0.473 |
DOC_PP1_RVXF_1 | 334 | 341 | PF00149 | 0.682 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.660 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.494 |
DOC_PP4_MxPP_1 | 140 | 143 | PF00568 | 0.699 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 88 | 92 | PF12436 | 0.674 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 215 | 223 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 31 | 41 | PF00244 | 0.551 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_DLG_GKlike_1 | 128 | 135 | PF00625 | 0.542 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.696 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.542 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.626 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.597 |
LIG_LIR_Gen_1 | 110 | 117 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.671 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.469 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.558 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.661 |
LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.665 |
LIG_SH3_2 | 87 | 92 | PF14604 | 0.585 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.742 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.615 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.494 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.595 |
LIG_SUMO_SIM_anti_2 | 19 | 25 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 134 | 139 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 49 | 54 | PF11976 | 0.519 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.775 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.495 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.687 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.833 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.782 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.492 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.704 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.830 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.628 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.816 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.656 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.676 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.670 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.796 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.539 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.796 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.715 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.791 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.778 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.548 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.529 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.690 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.477 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.783 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.682 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.722 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.606 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.487 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.742 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.643 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.765 |
MOD_SUMO_rev_2 | 214 | 223 | PF00179 | 0.806 |
MOD_SUMO_rev_2 | 35 | 40 | PF00179 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 69 | 74 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.732 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HZV2 | Leishmania infantum | 83% | 100% |