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: A4HX42
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.656 |
CLV_PCSK_FUR_1 | 158 | 162 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.468 |
CLV_PCSK_PC7_1 | 102 | 108 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.743 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.659 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.665 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.560 |
DOC_MAPK_gen_1 | 238 | 247 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 296 | 304 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.601 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.485 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.492 |
LIG_BIR_III_4 | 187 | 191 | PF00653 | 0.578 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.644 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.690 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.502 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.401 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.425 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.692 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.559 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.495 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.432 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.428 |
LIG_LIR_Gen_1 | 14 | 23 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 272 | 282 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.707 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.529 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.402 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.659 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.510 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.632 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.622 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.717 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.516 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.687 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.588 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.495 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.510 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.428 |
MOD_Cter_Amidation | 100 | 103 | PF01082 | 0.484 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.655 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.688 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.574 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.638 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.777 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.572 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.767 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.448 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.531 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.485 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.688 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.503 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.649 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.439 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.522 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.727 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.679 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.470 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.403 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.689 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.570 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.486 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.689 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.602 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.432 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.500 |
MOD_PKB_1 | 164 | 172 | PF00069 | 0.673 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.435 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.505 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.500 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.455 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.505 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.576 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.778 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.710 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.652 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.786 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.756 |
TRG_Pf-PMV_PEXEL_1 | 157 | 162 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT54 | Leptomonas seymouri | 33% | 94% |
A0A3S5H6Z1 | Leishmania donovani | 100% | 100% |
E9AQV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QEM0 | Leishmania major | 87% | 100% |