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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HGZ8
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.612 |
CLV_PCSK_FUR_1 | 5 | 9 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.477 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.495 |
DEG_COP1_1 | 230 | 238 | PF00400 | 0.506 |
DOC_CYCLIN_RxL_1 | 36 | 46 | PF00134 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 214 | 220 | PF00134 | 0.665 |
DOC_MAPK_gen_1 | 39 | 45 | PF00069 | 0.473 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.692 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.317 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.414 |
DOC_USP7_MATH_2 | 11 | 17 | PF00917 | 0.706 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.573 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.709 |
LIG_EVH1_2 | 27 | 31 | PF00568 | 0.521 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.532 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.428 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.397 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.413 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.472 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.594 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.659 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.354 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.652 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.639 |
LIG_IBAR_NPY_1 | 319 | 321 | PF08397 | 0.559 |
LIG_LIR_Gen_1 | 187 | 198 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 30 | 37 | PF02991 | 0.272 |
LIG_LIR_LC3C_4 | 116 | 121 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.267 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.721 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.361 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.280 |
MOD_CDK_SPxxK_3 | 176 | 183 | PF00069 | 0.573 |
MOD_CDK_SPxxK_3 | 268 | 275 | PF00069 | 0.679 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.483 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.568 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.574 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.579 |
MOD_GlcNHglycan | 109 | 113 | PF01048 | 0.533 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.546 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.460 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.677 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.506 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.508 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.724 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.585 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.678 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.652 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.604 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.486 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.425 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.629 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.321 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.684 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.649 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.578 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.394 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.744 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.515 |
MOD_PKB_1 | 70 | 78 | PF00069 | 0.499 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.702 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.621 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.579 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.510 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.368 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.579 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.756 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.565 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.592 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 208 | 211 | PF00179 | 0.587 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3L5 | Leptomonas seymouri | 66% | 100% |
A0A1X0NQH6 | Trypanosomatidae | 39% | 100% |
A0A3S5IR49 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X224 | Leishmania donovani | 83% | 99% |
A4I430 | Leishmania infantum | 83% | 99% |
E9B0B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4Q7W7 | Leishmania major | 84% | 100% |
V5BI47 | Trypanosoma cruzi | 44% | 100% |