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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HAZ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.769 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.855 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 137 | 141 | PF03568 | 0.571 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.578 |
DEG_SCF_FBW7_1 | 64 | 71 | PF00400 | 0.570 |
DEG_SCF_FBW7_2 | 261 | 266 | PF00400 | 0.566 |
DOC_ANK_TNKS_1 | 100 | 107 | PF00023 | 0.630 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.711 |
DOC_CYCLIN_RxL_1 | 74 | 85 | PF00134 | 0.560 |
DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.616 |
DOC_PP2B_LxvP_1 | 136 | 139 | PF13499 | 0.572 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.616 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 109 | 114 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.675 |
LIG_Actin_WH2_2 | 79 | 96 | PF00022 | 0.560 |
LIG_BIR_III_2 | 247 | 251 | PF00653 | 0.563 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.540 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.713 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.569 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.645 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.567 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.530 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.536 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.708 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.744 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.511 |
LIG_PDZ_Class_2 | 343 | 348 | PF00595 | 0.553 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.679 |
LIG_SH3_1 | 59 | 65 | PF00018 | 0.698 |
LIG_SH3_2 | 65 | 70 | PF14604 | 0.656 |
LIG_SH3_2 | 7 | 12 | PF14604 | 0.551 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.540 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.545 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.777 |
LIG_SUMO_SIM_anti_2 | 157 | 165 | PF11976 | 0.618 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 228 | 236 | PF11976 | 0.628 |
LIG_UBA3_1 | 318 | 324 | PF00899 | 0.504 |
LIG_WW_3 | 9 | 13 | PF00397 | 0.562 |
MOD_CDK_SPK_2 | 325 | 330 | PF00069 | 0.607 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.712 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.658 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.561 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.600 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.576 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.702 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.627 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.705 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.530 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.594 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.733 |
MOD_DYRK1A_RPxSP_1 | 259 | 263 | PF00069 | 0.566 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.644 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.606 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.718 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.634 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.620 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.601 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.670 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.537 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.628 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.537 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.705 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.581 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.641 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.673 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.567 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.519 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.552 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.578 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.594 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.712 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.572 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.677 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.541 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.568 |
MOD_Plk_2-3 | 275 | 281 | PF00069 | 0.573 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.562 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.704 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.549 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.566 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.612 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.712 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.568 |
TRG_NES_CRM1_1 | 183 | 194 | PF08389 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7X2 | Leishmania donovani | 53% | 100% |
A4IA53 | Leishmania infantum | 53% | 100% |
E9B567 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
Q4Q2R8 | Leishmania major | 51% | 98% |