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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AKB6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008176 | tRNA (guanine-N7-)-methyltransferase activity | 7 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 306 | 310 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.393 |
CLV_PCSK_FUR_1 | 282 | 286 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.491 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.590 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.621 |
DEG_ODPH_VHL_1 | 103 | 116 | PF01847 | 0.539 |
DOC_CYCLIN_RxL_1 | 124 | 134 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 289 | 298 | PF00069 | 0.585 |
DOC_PP1_RVXF_1 | 111 | 118 | PF00149 | 0.486 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.383 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.491 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.496 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.530 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 312 | 319 | PF00244 | 0.574 |
LIG_APCC_ABBA_1 | 228 | 233 | PF00400 | 0.525 |
LIG_APCC_ABBAyCdc20_2 | 126 | 132 | PF00400 | 0.243 |
LIG_APCC_ABBAyCdc20_2 | 201 | 207 | PF00400 | 0.487 |
LIG_Clathr_ClatBox_1 | 203 | 207 | PF01394 | 0.480 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.484 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.419 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.594 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.390 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.521 |
LIG_LIR_Gen_1 | 134 | 144 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.472 |
LIG_LIR_LC3C_4 | 136 | 140 | PF02991 | 0.438 |
LIG_LIR_LC3C_4 | 247 | 252 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.469 |
LIG_MAD2 | 214 | 222 | PF02301 | 0.323 |
LIG_NRBOX | 31 | 37 | PF00104 | 0.563 |
LIG_OCRL_FandH_1 | 192 | 204 | PF00620 | 0.549 |
LIG_REV1ctd_RIR_1 | 161 | 170 | PF16727 | 0.462 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.640 |
LIG_SH3_1 | 219 | 225 | PF00018 | 0.474 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.389 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.438 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.337 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.474 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 49 | 56 | PF11976 | 0.621 |
LIG_UBA3_1 | 241 | 249 | PF00899 | 0.491 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.423 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.473 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.492 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.495 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.468 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.416 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.528 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.336 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.473 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.431 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.424 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.502 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.457 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.553 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.389 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.523 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.609 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.468 |
MOD_OFUCOSY | 167 | 173 | PF10250 | 0.419 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.629 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.608 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.521 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.399 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.455 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.533 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.518 |
MOD_SUMO_rev_2 | 243 | 251 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_4 | 293 | 299 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.559 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 127 | 132 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N8 | Leptomonas seymouri | 67% | 100% |
A0A1X0P3K8 | Trypanosomatidae | 42% | 98% |
A0A3S5H5F9 | Leishmania donovani | 95% | 100% |
A0A3S5ISB0 | Trypanosoma rangeli | 47% | 100% |
A4H458 | Leishmania braziliensis | 88% | 100% |
A4HSE1 | Leishmania infantum | 95% | 100% |
C9ZPX1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q4QJJ1 | Leishmania major | 93% | 100% |
V5AUY0 | Trypanosoma cruzi | 43% | 100% |