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. | yes | yes: 15 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AQV4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.621 |
DOC_MAPK_DCC_7 | 287 | 295 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 146 | 155 | PF00069 | 0.666 |
DOC_MAPK_gen_1 | 50 | 58 | PF00069 | 0.641 |
DOC_MAPK_MEF2A_6 | 236 | 244 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 287 | 295 | PF00069 | 0.372 |
DOC_MAPK_RevD_3 | 237 | 253 | PF00069 | 0.376 |
DOC_PP1_RVXF_1 | 297 | 304 | PF00149 | 0.565 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.703 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.763 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.723 |
LIG_EH1_1 | 223 | 231 | PF00400 | 0.467 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.401 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.531 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.573 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.724 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.608 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.573 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 132 | 136 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.511 |
LIG_SH3_2 | 291 | 296 | PF14604 | 0.380 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.589 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 328 | 334 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 328 | 334 | PF11976 | 0.530 |
LIG_TRFH_1 | 58 | 62 | PF08558 | 0.627 |
LIG_UBA3_1 | 152 | 158 | PF00899 | 0.534 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.737 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.628 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.586 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.561 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.706 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.487 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.383 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.600 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.664 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.721 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.436 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.553 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.555 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.684 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.547 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.728 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.591 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.559 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.712 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.681 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.534 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.733 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.483 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.609 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.453 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.638 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.733 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.752 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.559 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.658 |
MOD_SUMO_for_1 | 286 | 289 | PF00179 | 0.674 |
TRG_DiLeu_BaEn_2 | 84 | 90 | PF01217 | 0.625 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 144 | 156 | PF08389 | 0.696 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBL8 | Leptomonas seymouri | 60% | 69% |
A0A1X0NYW3 | Trypanosomatidae | 43% | 100% |
A0A3R7JY16 | Trypanosoma rangeli | 36% | 94% |
A0A3S7WU51 | Leishmania donovani | 92% | 100% |
A4H8S0 | Leishmania braziliensis | 77% | 100% |
A4HX38 | Leishmania infantum | 91% | 100% |
Q4QEM4 | Leishmania major | 90% | 100% |
V5BMN4 | Trypanosoma cruzi | 40% | 96% |