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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4I0G0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0016462 | pyrophosphatase activity | 5 | 1 |
| GO:0016787 | hydrolase activity | 2 | 1 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
| GO:0047710 | bis(5'-adenosyl)-triphosphatase activity | 6 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.625 |
| CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.381 |
| CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.601 |
| CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.577 |
| CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.324 |
| CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.601 |
| CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.587 |
| CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.535 |
| CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.538 |
| DEG_COP1_1 | 81 | 91 | PF00400 | 0.661 |
| DEG_SCF_FBW7_2 | 169 | 174 | PF00400 | 0.499 |
| DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.508 |
| DEG_SPOP_SBC_1 | 343 | 347 | PF00917 | 0.551 |
| DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.746 |
| DOC_CKS1_1 | 319 | 324 | PF01111 | 0.618 |
| DOC_CYCLIN_RxL_1 | 330 | 340 | PF00134 | 0.524 |
| DOC_PP1_RVXF_1 | 235 | 241 | PF00149 | 0.443 |
| DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.597 |
| DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.526 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.550 |
| DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.379 |
| DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.324 |
| DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.523 |
| DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.605 |
| DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.776 |
| DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.507 |
| DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.647 |
| DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.508 |
| DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.682 |
| DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.562 |
| DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.626 |
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.607 |
| LIG_14-3-3_CanoR_1 | 178 | 182 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.517 |
| LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.533 |
| LIG_AP2alpha_2 | 90 | 92 | PF02296 | 0.481 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
| LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.573 |
| LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.490 |
| LIG_deltaCOP1_diTrp_1 | 233 | 240 | PF00928 | 0.443 |
| LIG_FHA_1 | 168 | 174 | PF00498 | 0.504 |
| LIG_FHA_1 | 18 | 24 | PF00498 | 0.693 |
| LIG_FHA_1 | 240 | 246 | PF00498 | 0.484 |
| LIG_FHA_1 | 262 | 268 | PF00498 | 0.590 |
| LIG_FHA_1 | 319 | 325 | PF00498 | 0.515 |
| LIG_FHA_1 | 327 | 333 | PF00498 | 0.445 |
| LIG_FHA_1 | 91 | 97 | PF00498 | 0.594 |
| LIG_FHA_2 | 114 | 120 | PF00498 | 0.632 |
| LIG_FHA_2 | 124 | 130 | PF00498 | 0.560 |
| LIG_FHA_2 | 226 | 232 | PF00498 | 0.530 |
| LIG_FHA_2 | 24 | 30 | PF00498 | 0.794 |
| LIG_FHA_2 | 76 | 82 | PF00498 | 0.757 |
| LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.472 |
| LIG_LIR_Apic_2 | 180 | 185 | PF02991 | 0.397 |
| LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.490 |
| LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.596 |
| LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.419 |
| LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.449 |
| LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.504 |
| LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.595 |
| LIG_SH2_CRK | 63 | 67 | PF00017 | 0.584 |
| LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.583 |
| LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.607 |
| LIG_SH2_SRC | 45 | 48 | PF00017 | 0.580 |
| LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.561 |
| LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.607 |
| LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.590 |
| LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.536 |
| LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.574 |
| LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.642 |
| LIG_SH3_1 | 316 | 322 | PF00018 | 0.631 |
| LIG_SH3_3 | 187 | 193 | PF00018 | 0.500 |
| LIG_SH3_3 | 204 | 210 | PF00018 | 0.355 |
| LIG_SH3_3 | 262 | 268 | PF00018 | 0.546 |
| LIG_SH3_3 | 293 | 299 | PF00018 | 0.490 |
| LIG_SH3_3 | 316 | 322 | PF00018 | 0.631 |
| LIG_SH3_3 | 85 | 91 | PF00018 | 0.693 |
| LIG_SH3_4 | 139 | 146 | PF00018 | 0.611 |
| LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.706 |
| LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.530 |
| LIG_TRFH_1 | 69 | 73 | PF08558 | 0.718 |
| LIG_WW_3 | 317 | 321 | PF00397 | 0.580 |
| MOD_CK1_1 | 167 | 173 | PF00069 | 0.636 |
| MOD_CK1_1 | 261 | 267 | PF00069 | 0.567 |
| MOD_CK2_1 | 103 | 109 | PF00069 | 0.691 |
| MOD_CK2_1 | 123 | 129 | PF00069 | 0.570 |
| MOD_CK2_1 | 225 | 231 | PF00069 | 0.490 |
| MOD_CK2_1 | 30 | 36 | PF00069 | 0.752 |
| MOD_CK2_1 | 75 | 81 | PF00069 | 0.761 |
| MOD_GlcNHglycan | 108 | 113 | PF01048 | 0.666 |
| MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.492 |
| MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.347 |
| MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.821 |
| MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.479 |
| MOD_GSK3_1 | 113 | 120 | PF00069 | 0.632 |
| MOD_GSK3_1 | 157 | 164 | PF00069 | 0.556 |
| MOD_GSK3_1 | 184 | 191 | PF00069 | 0.505 |
| MOD_GSK3_1 | 23 | 30 | PF00069 | 0.728 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.506 |
| MOD_GSK3_1 | 90 | 97 | PF00069 | 0.617 |
| MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.539 |
| MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.645 |
| MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.361 |
| MOD_NEK2_1 | 12 | 17 | PF00069 | 0.477 |
| MOD_NEK2_1 | 23 | 28 | PF00069 | 0.609 |
| MOD_NEK2_1 | 239 | 244 | PF00069 | 0.492 |
| MOD_NEK2_2 | 177 | 182 | PF00069 | 0.431 |
| MOD_NEK2_2 | 220 | 225 | PF00069 | 0.508 |
| MOD_PIKK_1 | 193 | 199 | PF00454 | 0.484 |
| MOD_PKA_1 | 3 | 9 | PF00069 | 0.590 |
| MOD_PKA_2 | 177 | 183 | PF00069 | 0.543 |
| MOD_PKA_2 | 23 | 29 | PF00069 | 0.674 |
| MOD_PKA_2 | 252 | 258 | PF00069 | 0.561 |
| MOD_PKA_2 | 3 | 9 | PF00069 | 0.587 |
| MOD_Plk_1 | 117 | 123 | PF00069 | 0.638 |
| MOD_Plk_1 | 271 | 277 | PF00069 | 0.561 |
| MOD_Plk_4 | 320 | 326 | PF00069 | 0.436 |
| MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.647 |
| MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.667 |
| MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.562 |
| MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.624 |
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.600 |
| TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.676 |
| TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.333 |
| TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.581 |
| TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.601 |
| TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.620 |
| TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.545 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P352 | Leptomonas seymouri | 57% | 81% |
| A0A1X0NWV2 | Trypanosomatidae | 39% | 77% |
| A0A3S7WXW4 | Leishmania donovani | 100% | 100% |
| A4HCX7 | Leishmania braziliensis | 83% | 100% |
| C9ZV80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 84% |
| E9AWC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
| Q4QB49 | Leishmania major | 93% | 100% |
| V5BJC2 | Trypanosoma cruzi | 45% | 86% |