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: A4I7N7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.684 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.579 |
DEG_Kelch_Keap1_1 | 110 | 115 | PF01344 | 0.272 |
DOC_CYCLIN_RxL_1 | 246 | 257 | PF00134 | 0.469 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 211 | 220 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 51 | 57 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 134 | 140 | PF00069 | 0.452 |
DOC_PP1_RVXF_1 | 192 | 199 | PF00149 | 0.347 |
DOC_PP1_RVXF_1 | 247 | 254 | PF00149 | 0.462 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.392 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 60 | 69 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 79 | 84 | PF00244 | 0.275 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.444 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.444 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.369 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.429 |
LIG_LIR_Gen_1 | 182 | 192 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.462 |
LIG_MAD2 | 60 | 68 | PF02301 | 0.429 |
LIG_NRP_CendR_1 | 294 | 296 | PF00754 | 0.544 |
LIG_PCNA_PIPBox_1 | 26 | 35 | PF02747 | 0.485 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.444 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.369 |
LIG_Pex14_2 | 200 | 204 | PF04695 | 0.532 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.369 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.599 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.344 |
LIG_UBA3_1 | 203 | 209 | PF00899 | 0.341 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.464 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.379 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.451 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.577 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.667 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.344 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.444 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.517 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.277 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.344 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.642 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.654 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.349 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.464 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.354 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.461 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.380 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.485 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.658 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.349 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.510 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.577 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.344 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.540 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.384 |
MOD_SUMO_for_1 | 167 | 170 | PF00179 | 0.349 |
MOD_SUMO_rev_2 | 130 | 136 | PF00179 | 0.454 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_4 | 230 | 236 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 34 | 39 | PF00026 | 0.296 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I881 | Leptomonas seymouri | 70% | 100% |
A0A0S4J6L8 | Bodo saltans | 31% | 78% |
A0A1X0NV53 | Trypanosomatidae | 45% | 100% |
A0A3S7X590 | Leishmania donovani | 100% | 100% |
A4HK51 | Leishmania braziliensis | 85% | 100% |
D0A9T8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B2J4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q5L2 | Leishmania major | 92% | 100% |