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: A0A3S7X039
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.488 |
DOC_MAPK_MEF2A_6 | 181 | 189 | PF00069 | 0.660 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.617 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.508 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.426 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.647 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.596 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.612 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.629 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.777 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.635 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.502 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.623 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.543 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.693 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.524 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.613 |
LIG_Integrin_isoDGR_2 | 40 | 42 | PF01839 | 0.549 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.632 |
LIG_LIR_Apic_2 | 55 | 59 | PF02991 | 0.578 |
LIG_LIR_LC3C_4 | 229 | 233 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.486 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.422 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.551 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.586 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.658 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.517 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.584 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.573 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.591 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.504 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.653 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.526 |
MOD_CDK_SPK_2 | 207 | 212 | PF00069 | 0.679 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.723 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.677 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.766 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.677 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.647 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.641 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.639 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.591 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.536 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.594 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.598 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.647 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.672 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.684 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.713 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.592 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.629 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.715 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.630 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.731 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.555 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.594 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.585 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.731 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.602 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.573 |
MOD_LATS_1 | 161 | 167 | PF00433 | 0.623 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.471 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.669 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.721 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.653 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.654 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.492 |
MOD_NEK2_2 | 30 | 35 | PF00069 | 0.608 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.592 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.579 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.599 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.586 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.620 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.803 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.472 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.493 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.695 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.704 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.596 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.696 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.646 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.573 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.484 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.556 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.535 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBU5 | Leptomonas seymouri | 49% | 97% |
A4HF52 | Leishmania braziliensis | 66% | 100% |
A4I2D6 | Leishmania infantum | 100% | 100% |
E9AYI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q8Y4 | Leishmania major | 89% | 100% |