Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 9 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A0A3Q8IDM9
Term | Name | Level | Count |
---|---|---|---|
GO:0000096 | sulfur amino acid metabolic process | 4 | 13 |
GO:0000097 | sulfur amino acid biosynthetic process | 5 | 13 |
GO:0006082 | organic acid metabolic process | 3 | 13 |
GO:0006520 | amino acid metabolic process | 3 | 13 |
GO:0006555 | methionine metabolic process | 5 | 13 |
GO:0006790 | sulfur compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0008652 | amino acid biosynthetic process | 4 | 13 |
GO:0009058 | biosynthetic process | 2 | 13 |
GO:0009066 | aspartate family amino acid metabolic process | 5 | 13 |
GO:0009067 | aspartate family amino acid biosynthetic process | 6 | 13 |
GO:0009086 | methionine biosynthetic process | 6 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016053 | organic acid biosynthetic process | 4 | 13 |
GO:0019509 | L-methionine salvage from methylthioadenosine | 6 | 8 |
GO:0019752 | carboxylic acid metabolic process | 5 | 13 |
GO:0043094 | cellular metabolic compound salvage | 3 | 8 |
GO:0043102 | amino acid salvage | 4 | 8 |
GO:0043436 | oxoacid metabolic process | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044249 | cellular biosynthetic process | 3 | 13 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 13 |
GO:0044281 | small molecule metabolic process | 2 | 13 |
GO:0044283 | small molecule biosynthetic process | 3 | 13 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 13 |
GO:0071265 | L-methionine biosynthetic process | 7 | 8 |
GO:0071267 | L-methionine salvage | 5 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 13 |
GO:1901576 | organic substance biosynthetic process | 3 | 13 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 13 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 8 |
GO:0005506 | iron ion binding | 6 | 8 |
GO:0010309 | acireductone dioxygenase [iron(II)-requiring] activity | 5 | 13 |
GO:0016491 | oxidoreductase activity | 2 | 13 |
GO:0016701 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen | 3 | 13 |
GO:0016702 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen | 4 | 13 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0046914 | transition metal ion binding | 5 | 8 |
GO:0051213 | dioxygenase activity | 3 | 13 |
GO:0010308 | acireductone dioxygenase (Ni2+-requiring) activity | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.646 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.684 |
DOC_CDC14_PxL_1 | 299 | 307 | PF14671 | 0.604 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.652 |
DOC_CYCLIN_RxL_1 | 212 | 222 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 200 | 206 | PF00134 | 0.629 |
DOC_MAPK_gen_1 | 223 | 230 | PF00069 | 0.524 |
DOC_MAPK_JIP1_4 | 224 | 230 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 201 | 210 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 223 | 232 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.571 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.704 |
DOC_PP2B_LxvP_1 | 274 | 277 | PF13499 | 0.677 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.662 |
DOC_USP7_MATH_2 | 277 | 283 | PF00917 | 0.622 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.673 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.687 |
LIG_APCC_ABBA_1 | 150 | 155 | PF00400 | 0.639 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.610 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.594 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.616 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.589 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.622 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.672 |
LIG_Integrin_isoDGR_2 | 193 | 195 | PF01839 | 0.564 |
LIG_LIR_Apic_2 | 2 | 8 | PF02991 | 0.627 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 27 | 36 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 319 | 330 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.646 |
LIG_Pex14_2 | 37 | 41 | PF04695 | 0.677 |
LIG_PTB_Apo_2 | 283 | 290 | PF02174 | 0.571 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.662 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.677 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.633 |
LIG_SH3_2 | 287 | 292 | PF14604 | 0.573 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.568 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.581 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.633 |
LIG_SH3_4 | 171 | 178 | PF00018 | 0.676 |
LIG_SUMO_SIM_anti_2 | 304 | 309 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 303 | 309 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 339 | 344 | PF11976 | 0.623 |
LIG_UBA3_1 | 197 | 205 | PF00899 | 0.643 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.662 |
MOD_CDK_SPxK_1 | 306 | 312 | PF00069 | 0.662 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.662 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.687 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.605 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.643 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.583 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.462 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.627 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.654 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.528 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.685 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.622 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.586 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.662 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.662 |
MOD_SUMO_rev_2 | 142 | 150 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 167 | 173 | PF00179 | 0.687 |
MOD_SUMO_rev_2 | 324 | 330 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_3 | 268 | 274 | PF01217 | 0.652 |
TRG_DiLeu_BaLyEn_6 | 117 | 122 | PF01217 | 0.677 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKW0 | Leptomonas seymouri | 72% | 100% |
A0A0S4JKP7 | Bodo saltans | 38% | 100% |
A0A1X0P434 | Trypanosomatidae | 32% | 100% |
A0A1X0P4C0 | Trypanosomatidae | 32% | 100% |
A0A422N1T2 | Trypanosoma rangeli | 32% | 100% |
A4HYT9 | Leishmania infantum | 99% | 100% |
D0A5U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AIE8 | Leishmania braziliensis | 88% | 100% |
E9AUN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QCU9 | Leishmania major | 92% | 100% |
V5D947 | Trypanosoma cruzi | 31% | 100% |