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: A4HRJ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.459 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.552 |
DEG_SCF_FBW7_1 | 165 | 172 | PF00400 | 0.691 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.672 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.693 |
DOC_CYCLIN_yClb3_PxF_3 | 165 | 171 | PF00134 | 0.623 |
DOC_MAPK_gen_1 | 126 | 136 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 14 | 20 | PF00149 | 0.534 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 129 | 134 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 293 | 302 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.480 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.591 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.566 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.640 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 296 | 302 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.438 |
LIG_LIR_LC3C_4 | 12 | 15 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.434 |
LIG_PDZ_Class_3 | 297 | 302 | PF00595 | 0.646 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.642 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.687 |
LIG_SUMO_SIM_par_1 | 131 | 138 | PF11976 | 0.649 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.579 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 235 | 241 | PF00069 | 0.665 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.605 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.616 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.751 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.739 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.654 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.622 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.592 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.587 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.646 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.644 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.699 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.697 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.753 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.606 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.620 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.583 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.619 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.623 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.636 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.609 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.705 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.620 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.610 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.715 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.713 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.626 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.622 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.576 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.807 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.531 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.679 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.619 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.651 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.645 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.617 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.786 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.760 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.691 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.597 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.692 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.665 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.625 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.567 |
MOD_PK_1 | 129 | 135 | PF00069 | 0.635 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.682 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.623 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.665 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.507 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.607 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.610 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.704 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.626 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.683 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.697 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.748 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.690 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.663 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I318 | Leptomonas seymouri | 43% | 93% |
A0A3S5H4W5 | Leishmania donovani | 99% | 100% |
A4H385 | Leishmania braziliensis | 70% | 92% |
E9AC58 | Leishmania major | 91% | 100% |
E9AJF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 95% |