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: Q4QGW8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.627 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.674 |
DEG_APCC_DBOX_1 | 41 | 49 | PF00400 | 0.624 |
DEG_SCF_FBW7_1 | 242 | 249 | PF00400 | 0.760 |
DOC_MAPK_MEF2A_6 | 318 | 327 | PF00069 | 0.646 |
DOC_PP4_FxxP_1 | 250 | 253 | PF00568 | 0.635 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 219 | 229 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.667 |
LIG_Actin_WH2_2 | 177 | 192 | PF00022 | 0.721 |
LIG_Actin_WH2_2 | 313 | 331 | PF00022 | 0.625 |
LIG_Actin_WH2_2 | 36 | 51 | PF00022 | 0.571 |
LIG_Actin_WH2_2 | 79 | 97 | PF00022 | 0.601 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.658 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.543 |
LIG_CtBP_PxDLS_1 | 231 | 235 | PF00389 | 0.531 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.637 |
LIG_EVH1_2 | 246 | 250 | PF00568 | 0.521 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.722 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.602 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.634 |
LIG_LIR_Apic_2 | 248 | 253 | PF02991 | 0.631 |
LIG_LIR_Apic_2 | 331 | 336 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.617 |
LIG_LYPXL_SIV_4 | 9 | 17 | PF13949 | 0.706 |
LIG_PDZ_Class_2 | 332 | 337 | PF00595 | 0.644 |
LIG_Rb_LxCxE_1 | 324 | 337 | PF01857 | 0.657 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.763 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.764 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.566 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.664 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.626 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.650 |
LIG_SUMO_SIM_anti_2 | 151 | 156 | PF11976 | 0.661 |
LIG_SUMO_SIM_anti_2 | 321 | 327 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.641 |
LIG_WRC_WIRS_1 | 103 | 108 | PF05994 | 0.657 |
MOD_CDK_SPK_2 | 138 | 143 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.677 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.734 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.759 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.723 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.467 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.605 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.665 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.674 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.767 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.542 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.743 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.463 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.706 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.399 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.722 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.670 |
MOD_GlcNHglycan | 306 | 310 | PF01048 | 0.518 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.529 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.433 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.473 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.700 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.675 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.603 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.646 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.660 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.770 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.545 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.580 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.514 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.488 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.520 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.674 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.749 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.486 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.630 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.726 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.713 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.645 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.603 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.705 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.704 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.619 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.641 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.522 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.657 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.744 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.676 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.761 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.656 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.636 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.637 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ79 | Leptomonas seymouri | 30% | 93% |
A0A3Q8I948 | Leishmania donovani | 90% | 100% |
A4H6N6 | Leishmania braziliensis | 63% | 100% |
A4HV20 | Leishmania infantum | 89% | 100% |
E8NHE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |