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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HCR1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.727 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.783 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.586 |
DEG_ODPH_VHL_1 | 163 | 176 | PF01847 | 0.422 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 157 | PF00134 | 0.517 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.654 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.508 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.765 |
LIG_Actin_WH2_2 | 300 | 318 | PF00022 | 0.590 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.801 |
LIG_EVH1_1 | 155 | 159 | PF00568 | 0.635 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.750 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.569 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.551 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.688 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.771 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.826 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.627 |
LIG_Integrin_isoDGR_2 | 242 | 244 | PF01839 | 0.564 |
LIG_LIR_Apic_2 | 119 | 123 | PF02991 | 0.805 |
LIG_LIR_Apic_2 | 77 | 81 | PF02991 | 0.492 |
LIG_MYND_1 | 153 | 157 | PF01753 | 0.720 |
LIG_PDZ_Class_2 | 339 | 344 | PF00595 | 0.663 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.500 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 78 | 82 | PF00017 | 0.538 |
LIG_SH2_SRC | 78 | 81 | PF00017 | 0.639 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.661 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.721 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.618 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.662 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.785 |
LIG_SUMO_SIM_par_1 | 173 | 179 | PF11976 | 0.616 |
MOD_CDC14_SPxK_1 | 47 | 50 | PF00782 | 0.551 |
MOD_CDK_SPxK_1 | 44 | 50 | PF00069 | 0.552 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.567 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.579 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.669 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.801 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.576 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.593 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.762 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.687 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.798 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.786 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.664 |
MOD_GlcNHglycan | 322 | 326 | PF01048 | 0.749 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.690 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.790 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.515 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.720 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.598 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.551 |
MOD_N-GLC_2 | 108 | 110 | PF02516 | 0.541 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.701 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.594 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.786 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.804 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.558 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.667 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.789 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.661 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.498 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.789 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.726 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.669 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.646 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.647 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.612 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.793 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.665 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.661 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.549 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.692 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.736 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.788 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.604 |
TRG_DiLeu_BaEn_2 | 337 | 343 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.786 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.498 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.792 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.791 |
TRG_Pf-PMV_PEXEL_1 | 301 | 305 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9J6 | Leptomonas seymouri | 35% | 100% |
A0A3S7WXL1 | Leishmania donovani | 61% | 99% |
A4I086 | Leishmania infantum | 62% | 99% |
E9AW50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 98% |
Q4QBC7 | Leishmania major | 62% | 100% |