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: Q4QBX2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.598 |
CLV_MEL_PAP_1 | 101 | 107 | PF00089 | 0.561 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.705 |
DOC_ANK_TNKS_1 | 243 | 250 | PF00023 | 0.685 |
DOC_CYCLIN_RxL_1 | 303 | 316 | PF00134 | 0.690 |
DOC_CYCLIN_yCln2_LP_2 | 97 | 103 | PF00134 | 0.655 |
DOC_PP1_RVXF_1 | 307 | 314 | PF00149 | 0.694 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.776 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.814 |
LIG_14-3-3_CterR_2 | 325 | 329 | PF00244 | 0.571 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.712 |
LIG_BIR_III_2 | 316 | 320 | PF00653 | 0.691 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.650 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.709 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.667 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.659 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.817 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.707 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.685 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.607 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.638 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.604 |
LIG_PDZ_Class_1 | 324 | 329 | PF00595 | 0.594 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.671 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.712 |
LIG_SUMO_SIM_par_1 | 70 | 78 | PF11976 | 0.631 |
LIG_SUMO_SIM_par_1 | 88 | 96 | PF11976 | 0.698 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.666 |
MOD_CDK_SPxxK_3 | 148 | 155 | PF00069 | 0.595 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.818 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.682 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.571 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.653 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.712 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.683 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.697 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.674 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.712 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.578 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.629 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.630 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.712 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.592 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.672 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.641 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.666 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.529 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.603 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.769 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.721 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.647 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.600 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.684 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.669 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.660 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.801 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.699 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.668 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.643 |
MOD_N-GLC_2 | 279 | 281 | PF02516 | 0.650 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.621 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.595 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.590 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.654 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.674 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.635 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.705 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.810 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.755 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.652 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.702 |
MOD_Plk_2-3 | 124 | 130 | PF00069 | 0.559 |
MOD_Plk_2-3 | 39 | 45 | PF00069 | 0.569 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.574 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.604 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.682 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.696 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.678 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.680 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.818 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.656 |
MOD_SUMO_rev_2 | 219 | 226 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.652 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7A5 | Leishmania donovani | 81% | 100% |
A4HC74 | Leishmania braziliensis | 52% | 74% |
A4HZQ1 | Leishmania infantum | 82% | 100% |
E9AVK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |