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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B0U6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.658 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.694 |
DOC_CYCLIN_RxL_1 | 79 | 91 | PF00134 | 0.406 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.719 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.560 |
LIG_AP2alpha_2 | 59 | 61 | PF02296 | 0.566 |
LIG_APCC_ABBA_1 | 177 | 182 | PF00400 | 0.500 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.607 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.599 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.646 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.555 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.572 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.471 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.616 |
LIG_LIR_Gen_1 | 167 | 173 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.739 |
LIG_Pex14_2 | 276 | 280 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 299 | 306 | PF02174 | 0.502 |
LIG_PTB_Phospho_1 | 299 | 305 | PF10480 | 0.498 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.529 |
LIG_SH3_1 | 155 | 161 | PF00018 | 0.387 |
LIG_SH3_2 | 150 | 155 | PF14604 | 0.538 |
LIG_SH3_2 | 158 | 163 | PF14604 | 0.463 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.522 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.549 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.548 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.788 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.466 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.556 |
LIG_TRFH_1 | 232 | 236 | PF08558 | 0.584 |
LIG_TYR_ITIM | 295 | 300 | PF00017 | 0.437 |
LIG_UBA3_1 | 99 | 106 | PF00899 | 0.446 |
LIG_WRC_WIRS_1 | 277 | 282 | PF05994 | 0.443 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.289 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.789 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.537 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.394 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.583 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.360 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.615 |
MOD_Cter_Amidation | 117 | 120 | PF01082 | 0.642 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.637 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.552 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.481 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.428 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.531 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.613 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.311 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.325 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.729 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.711 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.517 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.530 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.711 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.499 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.515 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.443 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.533 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.536 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.425 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.501 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.723 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.705 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.296 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.482 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.707 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.377 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.466 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.707 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.562 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.544 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.681 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.540 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.518 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.521 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.393 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.451 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.291 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.523 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.734 |
MOD_SUMO_rev_2 | 103 | 111 | PF00179 | 0.605 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.700 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT80 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IFU1 | Leishmania donovani | 84% | 100% |
A4HIB7 | Leishmania braziliensis | 67% | 100% |
A4I5K1 | Leishmania infantum | 83% | 100% |
Q4Q7C0 | Leishmania major | 84% | 100% |