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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7WRE9
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 2 |
GO:0032259 | methylation | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.460 |
DEG_MDM2_SWIB_1 | 220 | 227 | PF02201 | 0.470 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.456 |
DOC_MAPK_gen_1 | 225 | 235 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 228 | 237 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.401 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.461 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.347 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.455 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.334 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.313 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.405 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.469 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.321 |
LIG_LIR_Gen_1 | 125 | 136 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 141 | 147 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 20 | 30 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 265 | 276 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 302 | 311 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 42 | 49 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.562 |
LIG_Pex14_2 | 220 | 224 | PF04695 | 0.470 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.310 |
LIG_PTB_Phospho_1 | 247 | 253 | PF10480 | 0.305 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.305 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.341 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.295 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.295 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.456 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.320 |
LIG_SH3_5 | 138 | 142 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 290 | 295 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 232 | 238 | PF11976 | 0.294 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.418 |
LIG_TYR_ITSM | 18 | 25 | PF00017 | 0.459 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.461 |
MOD_CDK_SPK_2 | 26 | 31 | PF00069 | 0.462 |
MOD_CDK_SPxxK_3 | 26 | 33 | PF00069 | 0.462 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.208 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.417 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.469 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.498 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.427 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.305 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.384 |
MOD_Cter_Amidation | 11 | 14 | PF01082 | 0.458 |
MOD_Cter_Amidation | 52 | 55 | PF01082 | 0.444 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.483 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.294 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.504 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.614 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.471 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.284 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.450 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.459 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.404 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.343 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.424 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.400 |
MOD_N-GLC_2 | 69 | 71 | PF02516 | 0.401 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.440 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.233 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.356 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.329 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.475 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.525 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.535 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.413 |
MOD_PKB_1 | 31 | 39 | PF00069 | 0.462 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.281 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.512 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.503 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.388 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.503 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.337 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.344 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.462 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.455 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.437 |
MOD_SUMO_rev_2 | 108 | 115 | PF00179 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.447 |
TRG_ER_FFAT_2 | 198 | 208 | PF00635 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF1 | Leptomonas seymouri | 61% | 100% |
A4H6B4 | Leishmania braziliensis | 72% | 100% |
A4HUN7 | Leishmania infantum | 100% | 100% |
E9ACR1 | Leishmania major | 89% | 100% |
E9AND6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |