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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AUE4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.563 |
CLV_PCSK_FUR_1 | 305 | 309 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 140 | 146 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.399 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.473 |
DOC_CKS1_1 | 224 | 229 | PF01111 | 0.321 |
DOC_MAPK_RevD_3 | 184 | 198 | PF00069 | 0.411 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.768 |
DOC_USP7_UBL2_3 | 183 | 187 | PF12436 | 0.284 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 124 | 132 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 46 | 56 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.520 |
LIG_APCC_ABBAyCdc20_2 | 197 | 203 | PF00400 | 0.468 |
LIG_BRCT_BRCA1_1 | 178 | 182 | PF00533 | 0.564 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.553 |
LIG_Clathr_ClatBox_1 | 155 | 159 | PF01394 | 0.579 |
LIG_deltaCOP1_diTrp_1 | 39 | 45 | PF00928 | 0.676 |
LIG_eIF4E_1 | 161 | 167 | PF01652 | 0.429 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.487 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.595 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.546 |
LIG_LIR_Apic_2 | 97 | 103 | PF02991 | 0.687 |
LIG_LIR_Gen_1 | 216 | 227 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 256 | 264 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.676 |
LIG_MLH1_MIPbox_1 | 178 | 182 | PF16413 | 0.564 |
LIG_PDZ_Class_3 | 324 | 329 | PF00595 | 0.389 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.653 |
LIG_REV1ctd_RIR_1 | 179 | 187 | PF16727 | 0.333 |
LIG_RPA_C_Fungi | 241 | 253 | PF08784 | 0.545 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.665 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.643 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.327 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.327 |
LIG_Sin3_3 | 286 | 293 | PF02671 | 0.626 |
LIG_SUMO_SIM_par_1 | 154 | 159 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 72 | 79 | PF11976 | 0.473 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.463 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.384 |
LIG_UBA3_1 | 108 | 115 | PF00899 | 0.618 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.579 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.594 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.683 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.689 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.687 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.417 |
MOD_Cter_Amidation | 195 | 198 | PF01082 | 0.530 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.538 |
MOD_GlcNHglycan | 193 | 197 | PF01048 | 0.317 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.638 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.575 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.653 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.539 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.592 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.633 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.707 |
MOD_N-GLC_2 | 275 | 277 | PF02516 | 0.497 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.552 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.542 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.423 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.522 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.414 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.522 |
MOD_PKA_1 | 143 | 149 | PF00069 | 0.496 |
MOD_PKA_1 | 46 | 52 | PF00069 | 0.661 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.589 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.503 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.651 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.477 |
MOD_PKB_1 | 171 | 179 | PF00069 | 0.498 |
MOD_PKB_1 | 85 | 93 | PF00069 | 0.748 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.651 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.551 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.691 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 171 | 174 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.663 |
TRG_NLS_Bipartite_1 | 113 | 127 | PF00514 | 0.602 |
TRG_NLS_Bipartite_1 | 307 | 323 | PF00514 | 0.409 |
TRG_NLS_MonoExtN_4 | 317 | 323 | PF00514 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 198 | 203 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 307 | 312 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCL4 | Leptomonas seymouri | 40% | 100% |
A0A3Q8IBH2 | Leishmania donovani | 83% | 100% |
A0A3R7NEK1 | Trypanosoma rangeli | 26% | 100% |
A4HYJ7 | Leishmania infantum | 83% | 100% |
C9ZHU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
Q9BJ45 | Leishmania major | 82% | 100% |
V5BAF9 | Trypanosoma cruzi | 26% | 94% |