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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H4T5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016701 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen | 3 | 12 |
GO:0016702 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen | 4 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0051213 | dioxygenase activity | 3 | 12 |
GO:0047800 | cysteamine dioxygenase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.514 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.384 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.451 |
DEG_SCF_FBW7_1 | 174 | 181 | PF00400 | 0.354 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.354 |
DOC_CYCLIN_RxL_1 | 105 | 114 | PF00134 | 0.466 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.354 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.526 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.339 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 65 | 73 | PF00244 | 0.556 |
LIG_Actin_WH2_2 | 161 | 177 | PF00022 | 0.354 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.474 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.354 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.466 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.507 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.381 |
LIG_LIR_Apic_2 | 257 | 262 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 20 | 30 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.498 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.441 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.454 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.274 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.273 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.449 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.394 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.478 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.454 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.311 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.167 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.315 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.325 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.202 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.202 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.364 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.407 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.325 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.464 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.336 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.470 |
MOD_NEK2_2 | 87 | 92 | PF00069 | 0.264 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.331 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.167 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.439 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.260 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.363 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.348 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.297 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.422 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.281 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.400 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C5 | Leptomonas seymouri | 56% | 100% |
A0A0S4IQ52 | Bodo saltans | 30% | 100% |
A0A1X0NH28 | Trypanosomatidae | 40% | 100% |
A0A3S5H5U9 | Leishmania donovani | 81% | 92% |
A0A422NM88 | Trypanosoma rangeli | 33% | 100% |
A4HT14 | Leishmania infantum | 80% | 92% |
C9ZTQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AL02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 92% |
Q1G3U6 | Arabidopsis thaliana | 26% | 96% |
Q4QIV3 | Leishmania major | 78% | 100% |
V5BT74 | Trypanosoma cruzi | 42% | 100% |