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: A4HP64
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 11 |
GO:0070988 | demethylation | 2 | 11 |
GO:0070989 | oxidative demethylation | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0016491 | oxidoreductase activity | 2 | 4 |
GO:0032451 | demethylase activity | 2 | 1 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.258 |
CLV_PCSK_FUR_1 | 264 | 268 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.267 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.608 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.271 |
DOC_MAPK_gen_1 | 18 | 25 | PF00069 | 0.242 |
DOC_MAPK_gen_1 | 264 | 272 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 264 | 272 | PF00069 | 0.505 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 142 | 146 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.330 |
LIG_14-3-3_CanoR_1 | 240 | 244 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 266 | 271 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.393 |
LIG_APCC_ABBA_1 | 199 | 204 | PF00400 | 0.453 |
LIG_APCC_ABBA_1 | 99 | 104 | PF00400 | 0.379 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.556 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 204 | 209 | PF00928 | 0.453 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.393 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.360 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.538 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.386 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.455 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.449 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.453 |
LIG_LIR_Apic_2 | 225 | 229 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 53 | 64 | PF02991 | 0.358 |
LIG_LIR_LC3C_4 | 97 | 101 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.343 |
LIG_PDZ_Class_1 | 292 | 297 | PF00595 | 0.310 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.209 |
LIG_SH3_2 | 123 | 128 | PF14604 | 0.533 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.533 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.484 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.484 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.365 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.293 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.449 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.525 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.488 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.477 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.265 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.337 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.346 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.496 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.502 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.459 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.453 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.442 |
MOD_Cter_Amidation | 132 | 135 | PF01082 | 0.253 |
MOD_Cter_Amidation | 264 | 267 | PF01082 | 0.305 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.365 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.253 |
MOD_GlcNHglycan | 185 | 189 | PF01048 | 0.305 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.305 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.497 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.433 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.430 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.423 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.488 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.311 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.528 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.447 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.534 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.165 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.497 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.525 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.545 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.498 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.247 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.480 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.453 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.453 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.431 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.394 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.451 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.398 |
MOD_PKB_1 | 264 | 272 | PF00069 | 0.556 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.460 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.469 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.401 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.447 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.494 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.386 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.444 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.473 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.393 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.345 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.319 |
MOD_SUMO_for_1 | 74 | 77 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 187 | 197 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.473 |
TRG_NLS_Bipartite_1 | 134 | 152 | PF00514 | 0.453 |
TRG_NLS_MonoCore_2 | 145 | 150 | PF00514 | 0.467 |
TRG_NLS_MonoExtC_3 | 146 | 151 | PF00514 | 0.484 |
TRG_NLS_MonoExtN_4 | 143 | 150 | PF00514 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I860 | Leptomonas seymouri | 63% | 97% |
A0A0S4JT39 | Bodo saltans | 37% | 87% |
A0A1X0P7R1 | Trypanosomatidae | 46% | 100% |
A0A3Q8IH64 | Leishmania donovani | 81% | 100% |
A0A422N9C6 | Trypanosoma rangeli | 47% | 100% |
A4IDG9 | Leishmania infantum | 81% | 100% |
D0A357 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 98% |
E9ASX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q1M6 | Leishmania major | 79% | 100% |
Q8MNT9 | Caenorhabditis elegans | 33% | 100% |
Q8RWY1 | Arabidopsis thaliana | 29% | 86% |
Q9D8F1 | Mus musculus | 34% | 99% |
Q9NXW9 | Homo sapiens | 33% | 98% |