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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AMR9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.670 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.629 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.689 |
CLV_PCSK_PC7_1 | 193 | 199 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.571 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.611 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.645 |
DOC_MAPK_gen_1 | 193 | 203 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.639 |
DOC_MAPK_NFAT4_5 | 196 | 204 | PF00069 | 0.642 |
DOC_PP1_RVXF_1 | 349 | 356 | PF00149 | 0.613 |
DOC_PP2B_LxvP_1 | 199 | 202 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.707 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 114 | 118 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 243 | 252 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 327 | 334 | PF00244 | 0.717 |
LIG_CtBP_PxDLS_1 | 213 | 219 | PF00389 | 0.510 |
LIG_EVH1_1 | 310 | 314 | PF00568 | 0.708 |
LIG_EVH1_2 | 78 | 82 | PF00568 | 0.693 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.591 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.771 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.436 |
LIG_GBD_Chelix_1 | 127 | 135 | PF00786 | 0.590 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 251 | 257 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 241 | 245 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.429 |
LIG_NRBOX | 251 | 257 | PF00104 | 0.627 |
LIG_PCNA_yPIPBox_3 | 4 | 18 | PF02747 | 0.572 |
LIG_PROFILIN_1 | 311 | 317 | PF00235 | 0.671 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.677 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.522 |
LIG_SH3_1 | 308 | 314 | PF00018 | 0.770 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.695 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.669 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.688 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.636 |
LIG_SH3_5 | 238 | 242 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 231 | 237 | PF11976 | 0.715 |
LIG_WW_2 | 314 | 317 | PF00397 | 0.629 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.705 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.608 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.558 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.636 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.754 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.757 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.555 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.615 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.662 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.711 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.628 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.576 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.690 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.763 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.484 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.769 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.754 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.764 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.609 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.814 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.585 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.758 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.659 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.650 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.712 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.746 |
MOD_PKA_1 | 243 | 249 | PF00069 | 0.712 |
MOD_PKA_1 | 273 | 279 | PF00069 | 0.660 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.621 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.652 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.539 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.633 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.712 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.754 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.728 |
MOD_PKB_1 | 275 | 283 | PF00069 | 0.754 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.433 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.566 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.697 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.675 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.606 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.744 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.698 |
MOD_SUMO_rev_2 | 20 | 28 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 212 | 222 | PF00179 | 0.721 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.585 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.426 |
TRG_NLS_Bipartite_1 | 261 | 277 | PF00514 | 0.661 |
TRG_NLS_MonoExtC_3 | 272 | 277 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 270 | 277 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.726 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.715 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDE5 | Leptomonas seymouri | 43% | 94% |
A0A3Q8I7G4 | Leishmania donovani | 93% | 100% |
A4H5P9 | Leishmania braziliensis | 75% | 100% |
A4HTY9 | Leishmania infantum | 92% | 100% |
Q4QHV6 | Leishmania major | 92% | 100% |
V5BN47 | Trypanosoma cruzi | 26% | 100% |