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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9ASG6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.559 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.706 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.778 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.725 |
DOC_USP7_UBL2_3 | 123 | 127 | PF12436 | 0.516 |
DOC_USP7_UBL2_3 | 53 | 57 | PF12436 | 0.785 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 247 | 257 | PF00244 | 0.759 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.625 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.703 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.752 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.589 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 151 | 155 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 109 | 117 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.444 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.656 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.694 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.795 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.552 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.653 |
LIG_SH3_4 | 53 | 60 | PF00018 | 0.707 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.665 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.572 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.748 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.597 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.677 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.427 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.562 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.733 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.760 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.733 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.611 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.589 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.690 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.604 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.692 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.485 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.685 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.768 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.700 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.655 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.702 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.722 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.648 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.602 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.556 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.686 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.717 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.445 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.516 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.770 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.677 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.651 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.648 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.602 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.704 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.706 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.700 |
TRG_ER_FFAT_2 | 190 | 198 | PF00635 | 0.343 |
TRG_NLS_MonoExtC_3 | 126 | 132 | PF00514 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 330 | 334 | PF00026 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 81 | 86 | PF00026 | 0.624 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYW4 | Leptomonas seymouri | 57% | 94% |
A0A1X0P958 | Trypanosomatidae | 41% | 100% |
A0A3R7MA87 | Trypanosoma rangeli | 42% | 100% |
A0A3S7XAD7 | Leishmania donovani | 91% | 100% |
A4HNQ7 | Leishmania braziliensis | 76% | 98% |
A4ICT8 | Leishmania infantum | 91% | 100% |
Q4Q229 | Leishmania major | 92% | 100% |
V5BQI1 | Trypanosoma cruzi | 41% | 100% |