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: Q4QES9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 189 | 195 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.618 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.541 |
DEG_APCC_KENBOX_2 | 261 | 265 | PF00400 | 0.613 |
DEG_COP1_1 | 67 | 75 | PF00400 | 0.494 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.636 |
DOC_CYCLIN_RxL_1 | 74 | 84 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.559 |
DOC_PP1_RVXF_1 | 138 | 144 | PF00149 | 0.529 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.539 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.562 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 66 | 73 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 77 | 87 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.545 |
LIG_EH_1 | 31 | 35 | PF12763 | 0.558 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.565 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.605 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.424 |
LIG_PDZ_Class_3 | 293 | 298 | PF00595 | 0.582 |
LIG_Rb_LxCxE_1 | 117 | 138 | PF01857 | 0.470 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.543 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.611 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.563 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.605 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.595 |
LIG_SUMO_SIM_par_1 | 34 | 41 | PF11976 | 0.534 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.505 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.508 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.665 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.640 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.565 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.704 |
MOD_Cter_Amidation | 190 | 193 | PF01082 | 0.748 |
MOD_Cter_Amidation | 203 | 206 | PF01082 | 0.539 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.578 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.676 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.641 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.665 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.642 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.625 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.663 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.625 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.559 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.684 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.652 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.653 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.569 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.547 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.660 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.568 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.679 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.597 |
MOD_OFUCOSY | 64 | 70 | PF10250 | 0.568 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.565 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.466 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.605 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.551 |
MOD_PK_1 | 68 | 74 | PF00069 | 0.554 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.520 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.469 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.642 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.438 |
MOD_PKB_1 | 192 | 200 | PF00069 | 0.576 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.699 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.609 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.583 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.777 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 4 | 8 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P756 | Leptomonas seymouri | 35% | 96% |
A0A3S7WU02 | Leishmania donovani | 87% | 100% |
A4H8L3 | Leishmania braziliensis | 68% | 100% |
E9AGN6 | Leishmania infantum | 88% | 100% |
E9AQP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |