Uncharacterized Protein, Uncharacterized
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IGM9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.725 |
CLV_PCSK_FUR_1 | 140 | 144 | PF00082 | 0.627 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.630 |
DOC_CYCLIN_RxL_1 | 101 | 114 | PF00134 | 0.657 |
DOC_PP1_RVXF_1 | 105 | 112 | PF00149 | 0.655 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.688 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.671 |
DOC_USP7_MATH_2 | 207 | 213 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.727 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.641 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 13 | 17 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 132 | 138 | PF00244 | 0.612 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.661 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.545 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.607 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.755 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.641 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.546 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.628 |
LIG_LIR_Gen_1 | 177 | 183 | PF02991 | 0.732 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.732 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.650 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.714 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.689 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.658 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.762 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.705 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.602 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.708 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.622 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.699 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.543 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.720 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.638 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.545 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.599 |
MOD_DYRK1A_RPxSP_1 | 150 | 154 | PF00069 | 0.669 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.604 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.618 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.696 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.768 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.656 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.651 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.653 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.438 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.684 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.611 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.605 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.597 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.699 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.595 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.622 |
MOD_LATS_1 | 35 | 41 | PF00433 | 0.710 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.606 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.623 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.517 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.585 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.642 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.556 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.611 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.585 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.525 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.662 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.672 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.617 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.676 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.554 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.593 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.682 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.689 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.678 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.552 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.685 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.676 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.593 |
MOD_SUMO_rev_2 | 209 | 217 | PF00179 | 0.658 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.647 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 101 | 106 | PF00026 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS1 | Leptomonas seymouri | 56% | 95% |
A0A0S4JBY8 | Bodo saltans | 26% | 85% |
A0A422NYD6 | Trypanosoma rangeli | 41% | 88% |
A4HL47 | Leishmania braziliensis | 81% | 100% |
A4I8M6 | Leishmania infantum | 100% | 100% |
C9ZPV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 91% |
E9B3I8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q4L2 | Leishmania major | 92% | 100% |
V5BJG4 | Trypanosoma cruzi | 41% | 88% |