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: A4HZQ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.631 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.805 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.724 |
DOC_ANK_TNKS_1 | 243 | 250 | PF00023 | 0.778 |
DOC_CYCLIN_RxL_1 | 303 | 316 | PF00134 | 0.800 |
DOC_CYCLIN_yCln2_LP_2 | 97 | 103 | PF00134 | 0.738 |
DOC_PP1_RVXF_1 | 307 | 314 | PF00149 | 0.801 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.838 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.749 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.699 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.800 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.809 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.753 |
LIG_BIR_III_2 | 316 | 320 | PF00653 | 0.818 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.729 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.824 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.745 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.734 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.536 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.657 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.723 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.791 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.682 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.706 |
LIG_PAM2_1 | 46 | 58 | PF00658 | 0.569 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.622 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.683 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.764 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.824 |
LIG_Sin3_3 | 101 | 108 | PF02671 | 0.609 |
LIG_SUMO_SIM_par_1 | 70 | 78 | PF11976 | 0.700 |
LIG_SUMO_SIM_par_1 | 88 | 96 | PF11976 | 0.597 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.769 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.773 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.786 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.567 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.746 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.762 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.784 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.687 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.801 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.753 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.827 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.511 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.699 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.706 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.825 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.770 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.716 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.766 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.535 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.682 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.585 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.646 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.740 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.755 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.726 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.787 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.753 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.690 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.801 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.786 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.782 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.721 |
MOD_N-GLC_2 | 279 | 281 | PF02516 | 0.716 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.768 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.759 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.826 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.814 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.810 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.766 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.790 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.631 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.590 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.590 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.657 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.764 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.811 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.692 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.759 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.787 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.772 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.736 |
MOD_SUMO_rev_2 | 219 | 226 | PF00179 | 0.728 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.723 |
TRG_NLS_MonoExtC_3 | 52 | 58 | PF00514 | 0.676 |
TRG_NLS_MonoExtN_4 | 50 | 57 | PF00514 | 0.674 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7A5 | Leishmania donovani | 99% | 100% |
A4HC74 | Leishmania braziliensis | 53% | 100% |
E9AVK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QBX2 | Leishmania major | 82% | 100% |